Financial Statements

EXHIBIT 10.2
EXECUTION VERSION

SUPPLY AGREEMENT

     THIS SUPPLY AGREEMENT (the “AGREEMENT”), is made effective as of the 29^th day of June 2007 (the “EFFECTIVE DATE”) by and between InterMune, Inc. (“InterMune”), a California corporation, having an address at 3280 Bayshore Boulevard, Brisbane, California 94005, USA, and Boehringer Ingelheim Austria GmbH (“BI Austria”), an Austrian corporation, having its registered office at Dr. Boehringer-Gassge 5 – 11, A-1121 Vienna, Republic of Austria. InterMune and BI Austria may be referred to herein each individually as a “Party” and jointly as the “Parties.”

     WHEREAS, InterMune holds an exclusive sublicense under a license from GENENTECH (as defined herein) to manufacture, use and sell recombinant human gamma-interferon (“INTERFERON GAMMA 1b”, as further described herein) products in the USA and certain other territories, which INTERFERON GAMMA 1b is approved by the FDA for the indications Chronic Granulomatous Disease and severe, malignant Osteopetrois, and is sold in the USA under the trade-mark ACTIMMUNE^® (the “GENENTECH PRODUCT”, as further described herein); and

     WHEREAS, Boehringer Ingelheim International GmbH (BII), an affiliate of BI Austria and BI Pharma KG, holds an exclusive license from GENENTECH to manufacture, use and sell INTERFERON GAMMA 1b in certain other territories, and is the registration-holder for an INTERFERON GAMMA 1b product in certain countries for the indication Chronic Granulomatous Disease and is sold in Europe under the trade-mark IMUKIN^® (the “BI PRODUCT”, as further described herein); and

     WHEREAS, BI Austria and its affiliate BI Pharma KG (as defined hereinafter) own facilities specialized for cGMP manufacture of biopharmaceuticals and manufactures and supplies the BI PRODUCT to BII to meet BII’s needs with respect thereto; and

     WHEREAS, the Parties had entered into that certain Data Transfer, Clinical Trial and Market Supply Agreement dated the 27th of January 2000, as amended by the First Amendment dated the 19th of June 2002 (“Amendment No. 1”), Amendment No. 2 dated the 18th of September 2003 (“Amendment No. 2”), Amendment No. 3 dated the 26th of July 2005 (“Amendment No. 3”) and Amendment No. 4 dated the 21st of December 2006 (“Amendment No. 4”) (collectively, the “ORIGINAL SUPPLY AGREEMENT”) pursuant to which, among other things, (i) BI Austria conducted the activities necessary to show comparability between the GENENTECH PRODUCT and the BI PRODUCT for BI Austria to be registered with the FDA as a manufacturer for an INTERFERON GAMMA 1b product to be sold under the ACTIMMUNE^® trade-mark for the US market and other territories controlled by InterMune and (ii) BI Austria subsequently manufactured and supplied to InterMune finished INTERFERON GAMMA 1b product to meet InterMune’s needs with respect thereto; and

     WHEREAS, the Parties recently entered into that certain Termination Agreement dated the 6th of June 2007 (“TERMINATION AGREEMENT”) whereby the Parties agreed, among other things, to terminate the ORIGINAL SUPPLY AGREEMENT and enter into a new supply agreement to replace the ORIGINAL SUPPLY AGREEMENT; and

     WHEREAS, the Parties wish to enter into this AGREEMENT which shall constitute the “New Supply Agreement” for purposes of the TERMINATION AGREEMENT and which sets forth the terms and conditions pursuant to which BI Austria will continue on a going forward basis to manufacture and supply to InterMune and InterMune will purchase from BI Austria finished INTERFERON GAMMA 1b product to meet InterMune’s needs with respect thereto.

     NOW, THEREFORE, in consideration of the foregoing recitals which are hereby incorporated by reference herein and for other good and valuable consideration, the receipt and sufficiency of which is hereby acknowledged, the Parties hereto agree as follows:

1. Definitions

     The following capitalized definitions will apply throughout this Agreement:

1.1 AFFILIATE means (i) any corporation or business entity fifty percent (50 %) or more of the voting stock of which is and continues to be owned directly or indirectly by any party hereto; (ii) any corporation or business entity which directly or indirectly owns fifty percent (50 %) or more of the voting stock of any party hereto; or (iii) any corporation or business entity under the direct or indirect control of such corporation or business entity as described in (i) or (ii).

1.2 APPROVAL means a regulatory approval required from a HEALTH AUTHORITY in order to manufacture BBS or PRODUCT for use in clinical trials or market supply as applicable, in the applicable jurisdiction.

1.3 BI AUSTRIA’S IMPROVEMENTS shall mean all INFORMATION comprising any inventions, modifications and/or improvements to the INTERMUNE TECHNOLOGY or to the GENENTECH TECHNOLOGY, that BI Austria or BI Pharma KG conceive of or reduce to practice pursuant to the ORIGINAL SUPPLY AGREEMENT and/or this AGREEMENT, either individually or in conjunction with one or more third parties or BI Affiliates, including all patent and patent applications covering any of the foregoing.

1.4 BI AUSTRIA’S TECHNOLOGY means all INFORMATION in the field of manufacturing and testing of biopharmaceuticals, including without limitation the MANUFACTURING PROCESS but only to the extent that it relates solely to BI PRODUCT, and including all patents and patent applications covering any of the foregoing, that are owned or CONTROLLED by BI Austria or BI Pharma KG during the term of the ORIGINAL SUPPLY AGREEMENT and/or this AGREEMENT and that are related to or useful in BI Austria’s

carrying out its obligations under this AGREEMENT, but specifically excluding INTERMUNE’S TECHNOLOGY and BI AUSTRIA’S IMPROVEMENTS.

1.5 BII means Boehringer Ingelheim International GmbH, an AFFILIATE of BI Austria GmbH and BI Pharma KG.

1.6 BI PHARMA KG means BI Austria’s AFFILIATE BI Pharma KG, FRG-88397 Biberach an der Riss, Birkendorfer Straße 65, Germany, owning an FDA inspected and cGMP-certified facility.

1.7 BI PRODUCT means the liquid formulation of INTERFERON GAMMA 1b approved in various countries for which BII has acquired rights from GENENTECH for the treatment of Chronic Granulomatous Disease, and manufactured by BI Austria and BI Pharma KG for sale in Europe under the trademark IMUKIN^®.

1.8 BLA means a Biologics License Application, as defined by the regulations promulgated under the FD&C ACT, and any equivalent application with respective HEALTH AUTHORITIES.

1.9 BULK BIOLOGICAL SUBSTANCE (BBS) means a bulk form of the PRODUCT. This bulk form is the [*].

1.10 BULK SPECIFICATIONS mean the specifications for BBS listed in Exhibit 1.

1.11 cGMP means the current Good Manufacturing Practices of all applicable HEALTH AUTHORITIES, including without limitation the FDA, and including without limitation all applicable rules, regulations, guides and guidance, such as 21C.F.R. parts 210 and 211 and parts 600 and 610.

1.12 CMC means the Chemistry, Manufacturing, and Controls content of a submission to a HEALTH AUTHORITY.

1.13 COA means a Certificate of Analysis, a document listing testing parameters, specifications and test results (in a format and detail as listed in Exhibit 2).

1.14 COC means a Certificate of Compliance confirming compliance with cGMP regulations and signed by BI Austria’s authorized Qualified Person, the Head of Production and the Head of Quality Assurance (in a format and such detail as listed in Exhibit 3).

1.15 CONFIDENTIAL INFORMATION means any proprietary INFORMATION (a) disclosed by one Party to the other from and after the Effective Date hereof, or (b) developed by either Party pursuant to this AGREEMENT, except for INFORMATION which (i) is already in the public domain at the time of its disclosure to the receiving Party; (ii) becomes part of the

public domain through no wrongful action or omission of the receiving Party after disclosure to the receiving Party; (iii) is already known to the receiving Party at the time of disclosure as evidenced by the receiving Party’s written records; or (iv) is independently developed by the receiving Party without the use or application of the disclosing Party’s proprietary information.

1.16 CONTROLLED means, with respect to any material, INFORMATION or intellectual property right, possession of the ability by a Party to grant access, a license, or a sublicense to such material, INFORMATION or intellectual property right as provided for herein without violating an agreement with a Third Party as of the time such Party would be first required hereunder to grant the other Party such access, license or sublicense.

1.17 EURO means a euro, which is the European unit of currency.

1.18 FDA means the United States Food and Drug Administration and any successor agency thereto.

1.19 FD&C ACT means the United States Food, Drug & Cosmetic Act as amended from time to time and any supplements thereunder, and any equivalent regulation of any HEALTH AUTHORITIES.

1.20 FINAL RELEASE means the release of PRODUCT by InterMune or its licensees for clinical trial use or market supply, as applicable.

1.21 GENENTECH means Genetech, Inc. with its principle place of business at 1 DNA Way, South San Francisco, CA, 94080-4990.

1.22 GENENTECH PRODUCT means the formulation of INTERFERON GAMMA 1b which was manufactured in the US by GENENTECH for sale under the trademark ACTIMMUNE and approved by the FDA for the treatment of Chronic Granulomatous Disease and Osteopetrosis.

1.23 GENENTECH TECHNOLOGY means all INFORMATION relating to the manufacture, use or sale of INTERFERON GAMMA 1b that is licensed to either Party pursuant to an agreement with GENENTECH, including without limitation the MANUFACTURING PROCESS, and all patents and patent applications covering such INFORMATION.

1.24 HEALTH AUTHORITIES mean all regulatory authorities having jurisdiction over the manufacture, use and/or sale of the PRODUCT in the TERRITORY, including but not limited to the FDA.

1.25 INFORMATION means (a) techniques, data, inventions, practices, methods, knowledge, know-how, skill, experience, test data (including pharmacological, toxicological and clinical test data), analytical and quality control data, regulatory submissions, correspondence

and communications, marketing, pricing, distribution, cost, sales, manufacturing, patent and legal data or descriptions, compositions of matter, assays and biological materials, and (b) all intellectual property rights in and to any of the foregoing.

1.26 INTERFERON-GAMMA l b means the recombinant human Interferon-Gamma 1b derived from a [*], and that is the active ingredient in ACTIMMUNEÒ. The relevant amino acid sequence is set forth in Exhibit 4.

1.27 INTERMUNE’S TECHNOLOGY means all INFORMATION that is CONTROLLED by INTERMUNE during the term of the ORIGINAL SUPPLY AGREEMENT and/or the term of this AGREEMENT that is related to or useful in BI Austria’s manufacture of PRODUCT hereunder, and all patents and patent applications covering any of the foregoing; provided that “INTERMUNE’S TECHNOLOGY” shall not include any INFORMATION (i) owned or CONTROLLED by BI Austria prior to the Effective Date, (ii) conceived of, or reduced to practice or acquired by BI Austria outside the ORIGINAL SUPPLY AGREEMENT during the term thereof or outside this AGREEMENT during the term hereof, or (iii) the GENENTECH TECHNOLOGY.

1.28 MCB means the original Master Cell Bank derived from the [*] and established by GENENTECH.

1.29 MANUFACTURER’S RELEASE means the release of the PRODUCT by BI Austria to InterMune or its designee.

1.30 MANUFACTURING PROCESS means the process for fermentation, purification, filling, labeling and packaging of BBS and PRODUCT, as described in Exhibit 5.

1.31 MATERIAL SUPPLY BREACH means a failure of BI Austria: (a) to supply to InterMune at least [*] of InterMune’s binding forecasted requirements of PRODUCT (or actual orders, if less) that are due for delivery by the designated delivery date during the then-current calendar quarter; or (b) to repeatedly [*] materially violate against cGMP, as described in Sections 5.6 and 5.7.

1.32 ORIGINAL SUPPLY AGREEMENT has the meaning ascribed to it in the recitals of this AGREEMENT.

1.33 PRODUCT shall mean a finished product consisting of formulated INTERFERON GAMMA 1b filled into the designated containers for clinical supply and for market supply, as described in Exhibit 6, or shall mean a finished product of formulation buffer filled into the designated containers for clinical supply (placebo).

1.34 PROJECT MANAGER means the responsible person designated by each Party to be responsible for the communication of all information concerning this AGREEMENT. As of the

Effective Date, the person designated as InterMune’s PROJECT MANAGER and the person designated as BI Austria’s PROJECT MANAGER are listed in Exhibit 7. Either Party may change its own designated PROJECT MANAGER by providing written notice thereof to the other Party.

1.35 PRODUCT SPECIFICATIONS mean the specifications for the PRODUCT as set forth in Exhibit 8, or as otherwise agreed by the Parties in writing.

1.36 PROJECT TEAM means the team as listed in Exhibit 7 and described in Section 6.1.

1.37 QUALITY AGREEMENT means that Amended and Restated Quality Agreement dated the 15^th of December 2005 between the Parties.

1.38 QUALITY ASSURANCE REQUIREMENTS mean those requirements set forth in the QUALITY AGREEMENT.

1.39 STEERING COMMITTEE means the committee as listed in Exhibit 9 and as further described in Section 6.2.

1.40 TERMINATION AGREEMENT has the meaning ascribed to it in the recitals of this AGREEMENT.

1.41 TERRITORY means the US, Japan and all additional territories, including but not limited to Canada, as to which InterMune has or may acquire the right to manufacture, use or sell INTERFERON GAMMA 1b products during the term of this AGREEMENT.

1.42 US means the United States of America.

2. General

2.1 InterMune’s Tasks and Responsibilities

     2.1.1 Support

     InterMune shall timely send all documentation, and otherwise timely provide all information and other assistance, reasonably requested by BI Austria for use under this AGREEMENT. InterMune shall provide such reasonable technical support at its own expense, which support shall include access to InterMune’s expert personnel upon reasonable notice and at such reasonable times as the Parties may agree.

     2.1.2 Contact with Health Authorities

          2.1.2.1 InterMune, as the license holder for the GENENTECH PRODUCT in the US, shall have the overall responsibility regarding all contacts with the HEALTH AUTHORITIES and shall be solely responsible for filing all regulatory documents required by any HEALTH AUTHORITIES. BI Austria shall support InterMune in all matters regarding the manufacturing and quality control of PRODUCT as reasonably requested by InterMune, but InterMune shall be the leading Party, responsible for co-ordination of all regulatory matters.

          2.1.2.2 InterMune will notify BI Austria in due time, but in no event later than five (5) business days in advance of any meeting with any HEALTH AUTHORITIES with regard to manufacture, supply and quality control of the PRODUCT manufactured by BI Austria or BI Pharma KG under this AGREEMENT. BI Austria shall have the right to participate in such meetings with such HEALTH AUTHORITIES during the portion of such meetings relating to BI Austria’s or BI Pharma KG’s manufacture, supply and quality control of the PRODUCT.

          2.1.2.3 BI Austria will be responsible for drawing up the annual report required by the HEALTH AUTHORITIES reasonably in advance of the due date, and will be responsible of matters regarding the manufacture of PRODUCT. InterMune shall submit such report to the HEALTH AUTHORITIES and shall provide BI Austria with a copy of the finally submitted report.

     2.1.3 Shipment of Material by InterMune

     Any materials, e.g. samples, sent by InterMune (or by a third party on behalf of InterMune) to BI Austria shall be made by shipment from InterMune’s facility (or the third party’s facility, as the case may be) to BI Austria’s facility in Vienna. Shipping costs including insurance will be borne by InterMune, and risk of loss in transit shall lie with InterMune.

2.2 BI Austria’s Tasks and Responsibilities

     2.2.1 Regulatory Support

          2.2.1.1 BI Austria agrees to co-operate with InterMune in obtaining and maintaining all US governmental approvals and registrations relevant to the CMC section of the registration dossier (and their foreign equivalents) as requested by InterMune.

          2.2.1.2 The Parties shall consult with each other concerning the scope and content of all regulatory filings, and shall jointly define the requirements for the necessary PRODUCT registration with the FDA so that BI Austria shall be able to fulfill its obligations under this AGREEMENT with respect to the CMC portion of such PRODUCT registration. With respect to any part of the CMC portion which contain BI Austria and/or BI Pharma KG INFORMATION, BI Austria shall be provided an opportunity to review and comment on such parts prior to submission to a HEALTH AUTHORITY as set forth in the QUALITY AGREEMENT.

     2.2.2 Format and Content of Documents

     BI Austria’s Quality Management System demands a special format for certain documents (i.e. batch records, testing procedures, technical reports) which is binding. For those documents where a binding format is not obligatory the Parties shall agree in writing on a master format. With respect to the dates contained in these documents, and in particular in all reports and when dates occur in connection with signatures, the European writing style shall apply. The order shall be as follows: dd / mm / yy (day/month/year).

     2.2.3 [*] Production at [*] Versus [*]

     The Parties acknowledge and agree that as of the Effective Date hereof, BI Austria had developed a [*] process for production of BBS at [*] and has commenced production of BBS for InterMune at such a scale. The Parties have agreed that it is feasible to [*] to a [*] yield process for production of BBS at [*] given the [*] market demand of PRODUCT. As result, BI Austria shall, at its sole cost and expense, take all steps necessary to [*] the MANUFACTURING PROCESS to a [*] and to obtain any and all necessary process validation and APPROVALS for such [*] MANUFACTURING PROCESS. Upon receipt of the necessary process validation and APPROVALS for such scaled-down MANUFACTURING PROCESS, the Parties shall amend Exhibit 5 attached hereto to reflect the [*] process. During the process of obtaining the necessary process validation and APPROVALS for such [*] MANUFACTURING PROCESS, should a HEALTH AUTHORITY request additional certain PRODUCT-specific studies specifically for the PRODUCT to be supplied to InterMune and no HEALTH AUTHORITY requests such similar additional studies for the BI PRODUCT, InterMune shall bear the respective costs of such additional studies. In the event a HEALTH AUTHORITY requests additional studies for PRODUCT and the BI PRODUCT the Parties shall negotiate in good faith on sharing the cost for such studies.

3. Manufacture and Supply

3.1 General

     3.1.1 BI Austria shall [*] supply to InterMune BBS or PRODUCT for the treatment or prevention of any human disease or condition, except for the treatment or prevention of any type of cardiac or cardiovascular disease or condition. [*] BBS or PRODUCT for the treatment of any human disease or condition, except for the treatment or prevention of any type of cardiac or cardiovascular condition, [*]. InterMune shall [*] purchase from BI Austria, all of [*] for the term of this AGREEMENT, subject to Section 3.7. This provision does not in any way restrict [*].

     3.1.2 All BBS manufactured by BI Austria hereunder, and all PRODUCT manufactured and supplied to InterMune by BI Austria hereunder, shall be manufactured and supplied in

accordance with the BBS SPECIFICATIONS and PRODUCT SPECIFICATIONS, the cGMP requirements, the QUALITY ASSURANCE REQUIREMENTS as set forth in the QUALITY AGREEMENT and all applicable laws, regulations and ordinances of the jurisdiction in which such manufacture occurs.

     3.1.3 BI Austria shall manufacture BBS according to the BULK SPECIFICATIONS. BI Austria shall manufacture PRODUCT according to PRODUCT SPECIFICATIONS for clinical supply and for market supply. BBS for clinical and market supply shall be manufactured at BI Austria and transferred to BI Pharma KG for vialing, labeling (but only for market supply) and packaging. Manufacturing and filling of vials, labeling (but only for market supply) as well as the packaging and storing of PRODUCT shall be in accordance with the PRODUCT SPECIFICATIONS, the cGMP requirements, the QUALITY ASSURANCE REQUIREMENTS as set forth in the QUALITY AGREEMENT and all applicable laws, regulations and ordinances of the jurisdiction in which such manufacturing and/or filling occurs. Notwithstanding the fact that BI Austria takes BI Pharma KG as a toll manufacturer for filling, labeling (for market supply) and packaging of PRODUCT, BI Austria takes responsibility for the manufacture and supply of PRODUCT to InterMune in accordance with the terms and conditions of this AGREEMENT.

3.2 Forecasts

     3.2.1 Beginning with [*], unless otherwise agreed by the Parties, InterMune shall provide a rolling forecast for the next [*]. The first [*] of such forecast shall be firm (red zone). [*] shall be referred to as the blue zone. For [*] InterMune can reduce its forecast by [*] percent but only [*] in each [*], and may increase its forecast by [*] percent, but only [*] in each [*]. For [*] InterMune can reduce its forecast by [*] percent but only [*] in each [*], and may increase its forecast by [*] percent, but only [*] in each [*]. [*] will constitute a non-binding forecast (green zone). After the first forecast has been submitted by InterMune to BI Austria, successive forecasts shall be submitted on a [*] basis at the latest on every first day of every [*]. InterMune agrees to order the PRODUCT in filling lot quantities or multiples thereof (available lot sizes are 25.000 vials, or any other then available lot sizes). For purposes of clarity, the rolling forecast to be provided by InterMune under this Section 3.2 shall include the [*] vials that constitute the initial order of PRODUCTS described in Section 3.4 below.

     3.2.2 If InterMune requires more PRODUCT than is set forth in the current firm forecast, BI Austria shall use commercially reasonable efforts in good faith to supply InterMune with PRODUCT as requested; provided that for the amounts of PRODUCT in excess of such forecast which BI Austria is unable to supply, despite such commercially reasonable efforts, InterMune may use a secondary source manufacturer in accordance with the procedures set forth in Section 3.7.

     3.2.3 If InterMune reduces the forecast for [*] and [*] by an amount in excess of [*] percent (net of any increases in actual orders for these [*], then InterMune shall be [*] which was [*] in excess of the [*] percent reduction at the rate of [*] percent of the unit price of the PRODUCT then in effect. Similarly, if InterMune reduces the forecast for [*] by an amount in excess of [*] percent (net of any increases in actual orders for these [*], then InterMune shall be obligated to pay for PRODUCT which was not ordered in excess of the [*] percent reduction at the rate of [*] percent of the unit price of the PRODUCT then in effect.

3.3 Purchase Orders

     3.3.1 InterMune shall be obligated to purchase amounts of PRODUCT under this Agreement consistent with the binding/nonbinding rolling forecast set forth in Section 3.2 above. When purchasing PRODUCT hereunder, InterMune shall submit written purchase orders to BI Austria. To the extent that the terms of a purchase order or of BI Austria’s or BI Pharma KG’s “GENERAL CONDITIONS OF SALE” are inconsistent with the terms of this AGREEMENT, this AGREEMENT shall prevail.

     3.3.2 BI Austria shall guarantee that at the date of FINAL RELEASE all PRODUCT supplied to InterMune shall have a minimum residual shelf life of not less than [*] of PRODUCT shelf life, provided that InterMune shall strictly fulfill its contractual timelines regarding FINAL RELEASE as set forth in Sections 3.5 and 5.3.

     3.3.3 Subject to Section 3.4, BI Austria shall ship all PRODUCT as set forth in Section 3.5 by the date and in the quantities specified in the applicable purchase order. BI Austria shall be obligated to accept any purchase order within the range of permitted variation in the forecasted quantities as set forth in Section 3.2.1. and 3.2.2. Any other purchase order shall be binding on BI Austria only if it is accepted by BI Austria, which acceptance shall not be unreasonably withheld. If BI Austria does not accept such a purchase order, then InterMune may use a secondary source manufacturer for such purchase order in accordance with the procedures set forth in Section 3.7.

     3.3.4 InterMune shall be obligated to buy and BI Austria shall be obligated to sell only the quantities of PRODUCT which are subject to a purchase order accepted by BI Austria; provided that BI Austria shall accept sufficient purchase orders from InterMune annually to meet its obligations pursuant to Section 3.6.2 and in accordance with the rolling forecast model pursuant to Section 3.2.1. Any purchase order (or portion thereof) for which InterMune has not received a written rejection from BI Austria within thirty (30) business days of BI Austria’s receipt of such purchase order shall be deemed accepted by BI Austria. With respect to PRODUCTS ordered by InterMune for its clinical supply requirements, the number of vials supplied by BI Austria shall not exceed the number of vials subject to the applicable purchase order submitted by InterMune; provided, however, that if the number of vials BI Austria is able to supply falls below the number of vials ordered by InterMune in such purchase order and such

lesser number is within a reasonable range of the number ordered by InterMune, BI Austria shall notify InterMune in writing and inquire as to whether such lesser number of vials is acceptable and if not, whether BI Austria should produce an additional batch of BBS to produce enough vials to satisfy InterMune’s purchase order. If InterMune notifies BI Austria that such lesser number of vials is acceptable to InterMune, then the applicable purchase order shall be deemed to be amended to provide for such lesser number of vials and BI Austria shall be deemed to have accepted such purchase order in accordance with Section 3.3. On the other hand, if InterMune notifies BI Austria that BI Austria should manufacture an additional batch of BBS to produce the number of vials ordered by InterMune in its purchase order submitted to BI Austria, then BI Austria shall be obligated to produce the additional batch of BBS, InterMune shall be obligated to purchase any excess vials of PRODUCT produced by BI Austria from such additional batch of BBS and the purchase order submitted to BI Austria by InterMune shall be deemed amended to account for any excess vials resulting from the additional batch of BBS and such purchase order shall be deemed accepted by BI Austria in accordance with Section 3.3.

3.4 Initial Order

     The Parties acknowledge and agree that as of the Effective Date hereto, (i) InterMune has submitted to BI Austria and BI Austria has accepted a one-time purchase order for [*] vials of PRODUCT to be manufactured and delivered by BI Austria to InterMune in accordance with this AGREEMENT in the [*], and (ii) with respect to such [*] vials of PRODUCT, [*] set forth in the [*].

3.5 Shipment of Product and Material by BI Austria

     3.5.1 The PRODUCT and all material (e.g. samples) shall be shipped [*] either BI Pharma KG, FRG 88397 Biberach an der Riss, Germany or BI Austria’s facility in Vienna, Austria, as the case may be, to InterMune or as directed by InterMune, in accordance with Incoterms 2000 as published by the International Chamber of Commerce. InterMune’s designated carrier shall be used to ship PRODUCT to the site designated by InterMune. The Parties acknowledge and agree that the only deviation from the definition of [*] is that [*] shall be responsible and bear the cost of [*] the DRUG PRODUCT onto the [*] designated carrier such that [*] from BI Austria to InterMune only [*]. Risk of loss in transit by InterMune’s designated contract carrier shall lie with InterMune, except where such loss is caused by BI Austria’s or BI Pharma KG’s negligence.

     3.5.2 BI Austria will provide or will have provided assistance to InterMune regarding necessary procedures for exportation and/or importation of PRODUCT.

3.6 Testing and Rejection

     3.6.1 Within [*] business days of its receipt of PRODUCT at such destination as may be designated by InterMune, InterMune may perform such tests and samplings as are appropriate to determine whether such PRODUCT meets the applicable PRODUCT SPECIFICATIONS. If InterMune refuses acceptance of PRODUCT, then InterMune shall inform BI Austria in writing within [*] further business days of any aspect in which such PRODUCT fails to conform to the PRODUCT SPECIFICATIONS. If BI Austria does not receive such a notice within [*] business days of InterMune’s receipt of such PRODUCT, then InterMune shall be deemed to have accepted the PRODUCT; provided that InterMune shall have the right to revoke its acceptance of such goods if it later discovers latent defects not reasonably discoverable at the time of receipt.

     3.6.2 If BI Austria receives a notice from InterMune pursuant to Section 3.5.1 that InterMune does not accept any PRODUCT supplied hereunder, then BI Austria shall immediately start re-testing the PRODUCT using the retained samples in order to evaluate process issues and other reasons for such non-compliance.

     3.6.3 Regardless of whether BI Austria agrees with InterMune’s rejection of such PRODUCT, if requested in writing by InterMune, BI Austria shall use reasonable efforts to promptly replace such allegedly defective PRODUCT, the costs of which shall be borne as set forth in Section 3.6.4.

     3.6.4 In the event that BI Austria’s re-testing does not verify InterMune’s reasons for rejecting such PRODUCT and InterMune is convinced by BI Austria and agrees with BI Austria that InterMune’s reasons for rejecting such PRODUCT are unjustified , InterMune shall pay BI Austria reasonable internal and external costs for conducting such re-testing; provided, however, that, if InterMune is not convinced and does not agree that InterMune’s reasons for rejecting such PRODUCT are unjustified, the Parties shall mutually agree on an independent laboratory that shall determine by applying validated product-specific analytical methods whether such PRODUCT meets the PRODUCT SPECIFICATIONS. The conclusions of this independent laboratory shall be binding upon both Parties. If such laboratory determines that such PRODUCT does meet the PRODUCT SPECIFICATIONS, then InterMune shall bear the costs for such independent laboratory and for any replacement PRODUCT manufactured and supplied to InterMune by BI Austria pursuant to Section 3.6.3. If such laboratory determines that such PRODUCT does not meet the PRODUCT SPECIFICATIONS, then BI Austria shall bear the costs for such independent laboratory and for any such replacement of PRODUCT.

     3.6.5 Neither Party may destroy any PRODUCT alleged not to meet the PRODUCT SPECIFICATIONS until the independent laboratory determines whether such PRODUCT meets the applicable PRODUCT SPECIFICATIONS and provides written notification to the Parties with respect to such determination, unless BI Austria accepts InterMune’s basis for such rejection. Thereafter, BI Austria shall have the obligation to destroy or have destroyed, at its cost, all such rejected PRODUCT. Upon BI Austria’s written request and at BI Austria’s cost,

InterMune shall either destroy or return to BI Austria any rejected PRODUCT. The Parties agree that in the event of destruction of PRODUCT, the method of such destruction shall be in compliance with all applicable laws, rules and regulations.

     3.6.6 Claims on account of quantity, loss or damages to PRODUCT (other than claims that such PRODUCT does not meet the PRODUCT SPECIFICATIONS and latent defects not reasonably detectable upon inspection) will be dispatched by InterMune in writing within ten (10) business days following receipt thereof. BI Austria shall use reasonable efforts to replace the quantity of goods which such claims apply, which replacement shall be at InterMune’s expense unless such claims are due to the negligence of BI Austria.

3.7 Second Source Manufacturer

     3.7.1 BI Austria acknowledges that it is critical that InterMune be ensured continuity of supply of PRODUCT for use in clinical trials and market supply. BI Austria shall ensure continuity of supply of PRODUCT for use in clinical trials and market supply. Nevertheless, due to the potentially growing market demand of PRODUCT, BI Austria’s ability to manufacture and supply PRODUCT shall be carefully observed. Should at any time BI Austria have any indication that continuity of supply can not be ensured, BI Austria shall immediately inform InterMune thereof in writing. In this event the matter would be immediately forwarded to the STEERING COMMITTEE to discuss second source manufacture of PRODUCT reasonably and in good faith.

     3.7.2 In the event the STEERING COMMITTEE decides that it is appropriate for InterMune to establish a second source manufacturer, InterMune agrees to provide the first opportunity to qualify as a second source manufacturer for PRODUCT to a BI Austria AFFILIATE. If such an AFFILIATE is – as foreseeable — unable to supply InterMune’s PRODUCT requirements then InterMune shall be free to choose an alternate supplier. In this case BI Austria shall assist InterMune in transferring the MANUFACTURING PROCESS to a third party supplier by providing reasonable technical assistance and documentation as necessary for a transfer to a party well skilled in the manufacture of such biotech products at InterMune’s cost.

     3.7.3 In addition, the parties, through the STEERING COMMITTEE shall work together in good faith to develop a risk mitigation plan to minimize any risk of interruption in the supply of PRODUCT for use in clinical trials and market supply, which plan may include, among other things, production of excess PRODUCT or materials relating thereto (e.g., BBS) that can be used as a buffer and/or the off-site storage of certain PRODUCT or materials relating thereto.

3.8 Material Supply Breach

     3.8.1 In the event of a MATERIAL SUPPLY BREACH, InterMune shall provide BI Austria written notification of such MATERIAL SUPPLY BREACH. Upon BI Austria’s receipt of such notice and failure to cure such MATERIAL SUPPLY BREACH within the timetable and activity plan agreed upon the Parties to cure such MATERIAL SUPPLY BREACH, InterMune shall have the right to purchase from a second source manufacturer, to be agreed upon within the STEERING COMMITTEE in accordance with Section 3.7, such amounts of PRODUCT as necessary to offset BI Austria’s shortfall in fulfilling InterMune’s purchase orders for such PRODUCT (or the anticipated shortfall, in the event of repeated [*] material violation against cGMP).

     In the event, that

     (i) BI Austria AFFILIATE can not qualify as a second source manufacturer for PRODUCT or

     (ii) in the event such a BI Austria AFFILIATE is – as foreseeable — unable to supply InterMune’s PRODUCT requirements and

     (iii) provided that PRODUCT supply as requested by InterMune by a different second source manufacturer, a company experienced in manufacturing of biopharmaceuticals derived from [*], and selected by InterMune could demonstrably take place earlier than a MATERIAL SUPPLY BREACH by BI Austria could be remedied, BI Austria shall assist InterMune as requested in transferring the MANUFACTURING PROCESS to such a second source supplier, to be selected by InterMune by providing reasonable technical assistance and documentation relating to the manufacture, testing and supply of BBS and the PRODUCT as necessary at BI Austria’s cost. Such second source manufacturer would bear responsibility for putting the MANUFACTURING PROCESS in place. The total financial commitment for reasonable technical assistance shall not exceed the [*] for the period of [*].

     3.8.2 In the event that BI Austria reasonably anticipates that there is a substantial likelihood that a MATERIAL SUPPLY BREACH will occur, BI Austria shall promptly notify InterMune in writing thereof. Upon receipt of such notice, the Parties shall promptly confer to discuss the circumstances and magnitude of such potential MATERIAL SUPPLY BREACH, and to determine in good faith whether there are any reasonable steps that BI Austria could take to avoid such MATERIAL SUPPLY BREACH. If InterMune is not reasonably satisfied that BI Austria will be able to avoid such MATERIAL SUPPLY BREACH, then InterMune shall forward this issue to the STEERING COMMITTEE to determine whether it is necessary or desirable to establish a second source manufacturer in accordance with Section 3.7.

4. Prices and Payment

4.1 The prices to be paid by InterMune for the PRODUCT provided hereunder have been agreed to by the Parties. Initially, the price of PRODUCT for market supply shall be [*] for a unit of [*] vials of PRODUCT and the price of one single vial of PRODUCT for clinical supply shall be [*] (placebo [*]). Commencing [*], the price for the PRODUCT will be adjusted year by year in accordance with [*]. (By way of example, [*]. The price for 2005 will increase at [*].). Payments by InterMune to BI Austria under this AGREEMENT shall be in EUROS.

4.2 BI Austria will be entitled [*] prices [*] to BI Austria of [*] which are [*] PRODUCT at the time [*]. InterMune shall be entitled to have any [*] selected by InterMune and acceptable to BI Austria which [*] only. BI Austria shall provide InterMune with [*] days’ notice of any [*].

4.3 The price for PRODUCT or any services agreed by the Parties shall be paid to BI Austria no later than [*] days after the date that BI Austria’s invoice is received by InterMune. Payment of the invoice amounts shall be made in Austria, [*], into an account with such Austrian credit institution as shall be notified by BI Austria to InterMune from time to time.

4.4 All payments owed to BI Austria by InterMune on the basis of accounts rendered shall be made in such a way that [*] shall be [*] that are [*] invoice amounts (e.g. [*]). In the event of a default in payment for whatever reason, default interest at a rate of [*] p.a. shall be payable on the outstanding amount due. BI Austria reserves the right to claim any damage exceeding such amount that shall have been caused by such delay, subject to Section 11.1.

4.5 [*] owed to BI Austria by InterMune for the initial order of [*] vials of PRODUCT described in Section 3.4 above.

5. Quality Assurance and compliance with law

5.1 Manufacturer’s Release of Product

     5.1.1 BI Austria shall be responsible for the MANUFACTURER’S RELEASE of PRODUCT according to the PRODUCT SPECIFICATIONS, the cGMP requirements, the QUALITY ASSURANCE REQUIREMENTS as set forth in the QUALITY AGREEMENT and all applicable Austrian and German laws. BI Austria shall certify in writing that each shipment lot of PRODUCT was produced and tested in compliance with (i) the SPECIFICATIONS, (ii) the cGMP requirements (iii) QUALITY ASSURANCE REQUIREMENTS and (iv) all applicable laws, regulations and ordinances of the jurisdiction in which such manufacture occurs.

     5.1.2 BI Austria shall provide to InterMune, through BI Pharma KG, QUALITY ASSURANCE REQUIREMENTS as set forth in the QUALITY AGREEMENT including but not limited to a COA and COC signed by the appropriate personnel as defined in BI Austria’s Quality Management System for each shipment lot of PRODUCT from BI Pharma KG’s manufacture site in Biberach, Germany, in order to prove BI Austria’s compliance with the Article 5.1.1.

5.2 Storage of Records and Batch Samples

     5.2.1 BI Austria shall maintain in compliance with cGMP standards all batch samples and all records required by law or as otherwise mutually agreed in writing by the Parties (i.e. batch records, analytical raw data) necessary to evidence compliance with all its obligations under this AGREEMENT and relating to the manufacture of the BBS and of PRODUCT. The documentation concerning manufacture of BBS shall be stored at BI Austria and concerning manufacture of PRODUCT shall be stored in Biberach. Storage of retained samples of BBS as well as PRODUCT shall be at BI Austria or BI Pharma KG, as applicable.

     5.2.2 Copies of all documentation and information relating to the manufacture, processing, packaging and shipping of, BBS, PRODUCT and/or required to support InterMune’s BLA or other regulatory submissions, including but not limited to information relating to batch records, methods, equipment and the facility, will be provided by BI Austria to InterMune for review and inclusion as necessary in InterMune’s regulatory submissions.

     5.2.3 All such samples and records shall be maintained for a period not less than five (5) years from the date of expiration of each batch of PRODUCT to which such samples and records pertain, or such longer period as may be required by local law and the rules or regulations of the FDA or other applicable HEALTH AUTHORITIES. Following the expiration of such required retention period, prior to the destruction of any such sample or record, BI Austria shall give written notice thereof to InterMune, and InterMune shall have the right to request, receive and retain such samples and records with no further compensation to BI Austria.

5.3 Final Release

     FINAL RELEASE of PRODUCT supplied by BI Austria and/or BI Pharma KG hereunder for use in humans shall solely be made by and under the responsibility of InterMune.

5.4 Third Party Services

     Except as specifically provided for herein, BI Austria will not contract out to any third party the manufacture and testing of BBS or PRODUCT, without prior written approval from InterMune, which shall not be unreasonably withheld.

5.5 Consent to Changes

     BI Austria will not make any changes to BI Austria’s, and shall ensure that BI Pharma KG shall not make any changes to BI Pharma KG’s, respective manufacturing facilities, equipment, testing procedures, validation, suppliers of raw materials and components or documentation systems that are solely related to the BBS or PRODUCT and having a non-trivial impact on the BBS or PRODUCT, without the prior written consent of InterMune and solely as is permitted by cGMP. In the event that a supplier of raw material is unable to deliver the

respective raw material in time for scheduled manufacturing BI Austria is free to choose another supplier, provided that such supplier supplies such raw material that fully meets the respective raw material specification, and subject to BI Austria’s providing InterMune prior written notice thereof.

5.6 Inspections by Health Authorities

     5.6.1 BI Austria shall secure that during any inspections at BI Austria’s and/or BI Pharma KG’s facilities by any applicable HEALTH AUTHORITIES, BI Austria shall give InterMune prior written notice thereof promptly following BI Austria’s receipt of notice of such inspection, so that representatives of InterMune may attend and participate in such inspections, for example, to answer PRODUCT and any clinical trial related questions.

     5.6.2 BI Austria shall advise, and shall ensure that BI Pharma KG shall advise, InterMune in writing immediately of any requests by any applicable HEALTH AUTHORITIES for inspections at either of BI Austria’s or BI Pharma KG’s facilities, but in any event, no later than ten (10) business days prior to the scheduled date of such inspection. Upon reasonable notice, InterMune or its representatives may attend only such portions of such inspections or audits that deal with PRODUCT related issues, due to BI Austria’s other secrecy obligations. Access to such facilities may be subject to reasonable restrictions customarily placed upon visitors to the site.

     5.6.3 BI Austria also agrees to notify InterMune within [*] business days of any written or oral inquiries, notifications, or inspection activity by any HEALTH AUTHORITIES (or any third party authorized by the HEALTH AUTHORITIES) in regard to PRODUCT. BI Austria shall provide a reasonable description to InterMune of any such inquiries, notifications or inspections promptly (but in no event later than [*] business days) after such visit or inquiry. BI Austria shall furnish to InterMune (a) within [*] business days after receipt, any report or correspondence issued by the HEALTH AUTHORITIES (or a third party authorized by a HEALTH AUTHORITIES) in connection with such visit or inquiry, including but not limited to, any FDA Form 483 (List of Inspectional Observations) or warning letter, and (b) not later than five (5) business days prior to the time it provides to a HEALTH AUTHORITY, copies of any and all proposed written responses or explanations relating to items set forth above (each, a “Proposed Response”), in each case purged only of trade secrets or other confidential or proprietary information of BI Austria that are unrelated to its obligations under this AGREEMENT or are unrelated to PRODUCT. BI Austria shall discuss with InterMune any comments provided by InterMune on the Proposed Response; provided that InterMune shall have the final decision with respect to those portions of the final written response or explanation to be provided to the HEALTH AUTHORITIES that relate to PRODUCT manufactured hereunder. After the filing of a response with the appropriate HEALTH AUTHORITIES, BI Austria will notify InterMune of any further contacts with the HEALTH AUTHORITIES relating to BI Austria’s manufacture of PRODUCT hereunder.

     5.6.4 BI Austria shall promptly correct, and shall ensure that BI Pharma KG shall promptly correct, any facility-related violations or deficiencies promptly at its own expense. Equipment, system and process-related violations or deficiencies that are solely PRODUCT-related shall be corrected promptly by BI Austria or BI Pharma KG, respectively, at InterMune’s cost.

     In the event such corrections will not only be necessary for PRODUCT but as well for BI PRODUCT the appropriate allocation of the related costs between the Parties shall be determined by the PROJECT TEAM.

5.7 Audits by InterMune

     5.7.1 InterMune shall have the right to inspect and audit both of BI Austria’s and BI Pharma KG’s manufacturing facilities and records for regulatory compliance. These audits shall occur annually upon reasonable notice, and more frequently for good and reasonable cause. BI Austria shall respond in writing to InterMune regarding any items of non-compliance with cGMP identified by InterMune during such audits, whether with respect to the BI Austria or the BI Pharma KG facility, within [*] business days of InterMune’s notice thereof, and without delay remedy any such agreed upon items of non-compliance with cGMP.

     5.7.2 If BI Austria can not remedy such non-compliance, whether with respect to the BI Austria or the BI Pharma KG facility, within [*] business days of notice thereof BI Austria’s response shall include a written plan and timetable including reasonable timelines. Considering the fact that BI Austria is dependent on certain third parties to supply services to it, BI Austria shall use best efforts to assign such timelines to these third parties accordingly in order to meet all timelines for such remedy. Such plan and timetable shall be subject to InterMune’s approval, which shall not unreasonably be withheld. In the event that BI Austria does not respond with a plan and timetable as described above within such [*] day period, or InterMune does not approve such proposed plan and timetable for good reason, the issue shall be forwarded to the STEERING COMMITTEE for resolution. In the event InterMune approves such plan and timetable, but BI Austria fails to remedy such non-compliance in accordance with such plan and timetable, then InterMune shall have the right to terminate this AGREEMENT pursuant to Section 13.2.1.

5.8 Manufacturing Facilities

     BI Austria represents and warrants that it and BI Pharma KG shall obtain all relevant APPROVALS required by the relevant HEALTH AUTHORITIES for each of their respective manufacturing facilities and that each of their respective manufacturing facilities conform, and will during the term of this AGREEMENT conform, to the cGMP.

5.9 Compliance with Law

     5.9.1 BI Austria shall comply, and shall ensure that its subcontractor BI Pharma KG shall comply with, all local applicable rules, laws and regulations (including without limitation cGMP) in performing its obligations under this AGREEMENT. InterMune shall comply with all applicable rules, laws and regulations in performing its obligations under this AGREEMENT.

     5.9.2 All costs in connection with maintaining BI Austria’s and BI Pharma KG’s compliance with all applicable local regulatory requirements and cGMP in performing under this AGREEMENT, including but not limited to the maintenance and upgrading of all technical facilities and infrastructure and the training of personnel, shall be borne by BI Austria. BI Austria shall obtain and maintain, and shall ensure that BI Pharma KG obtains and maintains, all permits and licenses necessary to its performance under this AGREEMENT at their own expense. All costs in connection with any requirements by InterMune or a HEALTH AUTHORITY which relate specifically and solely to the PRODUCT (and not also to the BI PRODUCT) shall be solely borne by InterMune.

5.10 Environmental

     BI Austria shall, and shall ensure that BI Pharma KG shall, properly dispose of any and all hazardous waste materials involved with the manufacture of BBS and PRODUCT that are generated or resulting from the activities performed hereunder, if any, in full compliance with all applicable local laws and regulations at BI Austria’s sole liability and expense.

5.11 Quality Agreement

     The Parties hereby agree that the QUALITY AGREEMENT is hereby incorporated by reference herein and that it shall apply in full force to BBS and PRODUCT produced under this AGREEMENT. In the event of any conflict between this AGREEMENT and the QUALITY AGREEMENT, this AGREEMENT shall govern to the extent of such conflict except to the limited extent that a provision of the QUALITY AGREEMENT expressly and specifically states an intent to supersede.

6. Co-operation and co-ordination between the Parties

6.1 Project Team

     6.1.1 The day-to-day responsibilities of the Parties with respect to this AGREEMENT shall be overseen by the PROJECT TEAM, which shall be responsible for deciding operational and scientific issues arising out of this AGREEMENT and unanimously agreeing in good faith with respect to the monitoring of the compliance with this AGREEMENT.

     6.1.2 The PROJECT TEAM shall consist of a team consisting of equal numbers of people, if feasible, each appointed by InterMune and BI Austria and notified to the other, which appointees may be changed from time to time by the appointing Party on written notice to the

other Party. Each member of the PROJECT TEAM shall be a person of appropriate skill and experience. Either Party may change its own designated PROJECT TEAM members provided, however that the total number of members of the PROJECT TEAM may not be changed if feasible, nor the number of members representing InterMune decreased, without the Parties’ prior written agreement. InterMune’s and BI Austria’s respective members of the PROJECT TEAM as of the Effective Date are listed in Exhibit 7.

     6.1.3 During the term of this AGREEMENT, the PROJECT TEAM shall meet regularly to communicate updates and provide a forum for decision-making and rapid resolution of issues arising under this AGREEMENT. Meetings of the PROJECT TEAM may be conducted by telephone conference, videoconference or face-to-face meetings as agreed by the PROJECT TEAM, provided that the PROJECT TEAM shall meet at least once a year in a face-to-face meeting at a mutually agreed location.

     6.1.4 Decisions of the PROJECT TEAM shall be reflected in the approved minutes. Meeting minutes shall be prepared jointly by the PROJECT MANAGERS to record all issues discussed and decisions. Minutes that have not been objected to in writing by a Party within six (6) business days of receipt thereof shall be deemed approved by such Party and followed by issuance of two (2) copies of the minutes duly executed by the Parties’ PROJECT MANAGER.

     6.1.5 In the event that the PROJECT TEAM is unable to reach agreement on any issue and is unable to make decisions arising out of operational and scientific issues within ten (10) business days, each Party may call in an expert of its own choice to render advice to the PROJECT TEAM. Based on the advice of such expert(s) and the team members’ know-how, the PROJECT TEAM will try to resolve such issue. In the event that the PROJECT TEAM fails to reach agreement on an issue within thirty (30) business days of first undertaking resolution of such issue, such issue shall then be referred to the STEERING COMMITTEE for immediate resolution.

6.2 Steering Committee

     6.2.1 The Parties shall create a STEERING COMMITTEE consisting of the PROJECT MANAGER of each Party and authorized representatives who shall be appointed by InterMune and by BI Austria in equal numbers, if feasible, and notified to the other Party. The STEERING COMMITTEE shall be responsible for unanimously agreeing in good faith all issues on which the PROJECT TEAM has been unable to reach agreement and, where possible, make decisions arising out of such issues as well as carry out the specific functions, including but not limited to decisions with an impact on costs and timelines of any activities to be carried out under this AGREEMENT. Each Party may change its own designated STEERING COMMITTEE members by providing written notice thereof to the other Party; provided, however that the total number of members of the STEERING COMMITTEE may not be changed, if feasible, nor the number of

members representing InterMune decreased, without the Parties’ prior written agreement. The members of the STEERING COMMITTEE are listed in Exhibit 9.

     6.2.2 The STEERING COMMITTEE shall attempt in good faith to expeditiously and fairly resolve all issues before it. In the event that the STEERING COMMITTEE is unable to resolve any issue before it within fifteen (15) business days from the date that such issue is referred to it, such issue shall be referred to the Chief Executive Officer of InterMune and the Chief Executive Officer of BI Austria for prompt, good faith resolution. If such individuals do not reach agreement on such issue within fifteen (15) days of such referral, then each Party shall be free to pursue all available legal and/or equitable remedies.

6.3 Limitation of Powers

     The powers of the PROJECT TEAM and the STEERING COMMITTEE are limited to those expressly set forth in this AGREEMENT. Without limiting the generality of the foregoing, neither the PROJECT TEAM nor the STEERING COMMITTEE shall have the right to amend this AGREEMENT. The actions of the PROJECT TEAM and/or the STEERING COMMITTEE shall not substitute for either Party’s ability to exercise any right, nor excuse the performance of any obligation, set forth herein.

7. intellectual Property and Licenses

7.1 The ownership of INTERMUNE’S TECHNOLOGY and shall remain with InterMune and shall not vest in BI Austria.

7.2 The ownership of BI AUSTRIA’S TECHNOLOGY shall remain with BI Austria and shall not vest in InterMune.

7.3 BI Austria shall retain ownership of BI AUSTRIA’S IMPROVEMENTS. BI Austria hereby grants to InterMune a non exclusive, perpetual, sublicenseable, [*] license under BI AUSTRIA’S IMPROVEMENTS (i) to the extent necessary to develop, use, import, offer for sale and sell products containing INTERFERON GAMMA 1b in the name and on the account of InterMune in the TERRITORY, and (ii) in the event InterMune transfer the process to a second source manufacturer as permitted under this AGREEMENT, to make and have made products containing INTERFERON GAMMA 1b in the name and on account of InterMune in the TERRITORY, whereby in each case InterMune shall assume the costs to be paid by BI Austria for awards to inventors of BI AUSTRIA’S IMPROVEMENTS, as such awards are set forth in written agreements between BI Austria and such inventor or in an applicable industry labor contract or mandatory by Austrian laws.

7.4 The Parties shall each have an undivided one-half ownership interest in any INFORMATION jointly conceived of or reduced to practice by the Parties pursuant to the ORIGINAL SUPPLY AGREEMENT and/or this AGREEMENT (“JOINT INFORMATION”).

InterMune shall [*] of any JOINT INFORMATION that comprises (a) any regulatory filing (or documentation and raw data relating thereto) relating to PRODUCT manufactured hereunder or the ORIGINAL SUPPLY AGREEMENT, or (b) any manufacturing documentation (including without limitation batch records) relating to PRODUCT manufactured hereunder or the ORIGINAL SUPPLY AGREEMENT (“PRODUCT INFORMATION”). Upon request by InterMune, without additional consideration, BI Austria agrees to promptly execute documents, testify and take other acts at InterMune’s expense as InterMune may deem necessary or desirable to procure, maintain, perfect, and enforce the full benefits, enjoyment, rights, title and interest of the PRODUCT INFORMATION, on a worldwide basis. In the event InterMune is unable for any reason, after reasonable effort, to secure BI Austria’s signature on any document needed in connection with the actions specified in this Section 7.4, BI Austria hereby irrevocably designates and appoints InterMune and its duly authorized officers and agents as its agent and attorney in fact, which appointment is coupled with an interest, to act for and in its behalf to execute, verify and file any such documents and to do all other lawfully permitted acts to further the purposes of this Section 7.4 with the same legal force and effect as if executed by BI Austria.

7.5 InterMune hereby grants to BI Austria (with the right to sublicense solely to BI Pharma KG) a non-exclusive, nontransferable license to use INTERMUNE’S TECHNOLOGY solely for the purpose of manufacturing PRODUCT for InterMune, as provided in this AGREEMENT. The license granted under this Section shall automatically terminate upon the expiration or termination of this AGREEMENT.

7.6 New Indications

     7.6.1 In the event that InterMune receives approval in the TERRITORY to commercially sell PRODUCT for indications other than Chronic Granulomatous Disease and severe, malignant Osteopetrosis, and provided that InterMune has the right to grant a license to BII in the BI TERRITORY to make, use and sell PRODUCT for such additional indications (a “NEW INDICATIONS LICENSE”), InterMune shall provide BII written notice thereof.

     7.6.2 BII shall notify InterMune in writing within thirty (30) days of InterMune’s notice (the “NOTIFICATION PERIOD”) whether BII desires to obtain a NEW INDICATIONS LICENSE. If InterMune does not receive written notice from BII during the NOTIFICATION PERIOD that BII desires to obtain a NEW INDICATIONS LICENSE, then InterMune shall have no further obligations under this Section 7.6. If InterMune does receive written notice from BII that BII desires to obtain a NEW INDICATIONS LICENSE, then BII and InterMune shall engage in good faith negotiations for sixty (60) business days thereafter regarding the reasonable commercial terms upon which InterMune would be willing to grant such a license. If at the end of such sixty (60) business day period, BII and InterMune have not entered into a written agreement under which InterMune grants a NEW INDICATIONS LICENSE to BII, then InterMune shall have no further obligation under this Section 7.6.

8. Complaints; Adverse Events; Recalls

8.1 InterMune shall inform BI Austria of any complaints, adverse reaction reports, safety issues or toxicity issues relating to any PRODUCT of which it becomes aware, regardless of the origin of such information, within the time frame required by cGMP but in no event later than two (2) days from the initial complaint or report.

     8.1.1 InterMune shall retain and manage complaints in accordance with cGMP. The Parties hereby agree to cooperate with one another and with any HEALTH AUTHORITY in the evaluation and investigation of any complaint, claim or adverse reaction report related to the manufacture of such PRODUCT with the intention of complying with cGMP.

     8.1.2 If any such event occurs, BI Austria shall retain any unused supplies of such PRODUCT and its associated components, and all associated batch and other production records in such manner as InterMune may reasonably direct, and at InterMune’s expense, except to the extent such event is caused by BI Austria’s wrongful act or omission. BI Austria agrees to respond to InterMune in respect to such complaint investigations involving BI Austria’s manufacturing of a PRODUCT hereunder as soon as reasonably possible but in any case within thirty (30) days from receipt by BI Austria of the report of such complaint and sample (if available), or in the case of a serious adverse event, within ten (10) days from receipt of the report of such complaint and sample (if available). InterMune and/or its designee shall serve as the sole point of contact with the FDA or other applicable HEALTH AUTHORITY concerning any complaints, adverse reaction reports, safety issues or toxicity issues with respect to PRODUCT.

8.2 If either Party becomes aware at any time of any defect or the possibility of any defect associated with any PRODUCT manufactured by BI Austria hereunder, such Party will notify the other Party immediately and confirm the notification as soon as possible in writing.

8.3 InterMune shall notify BI Austria promptly if any PRODUCT manufactured by BI Austria hereunder is the subject of a recall, market withdrawal or correction, and InterMune and/or its designee shall have the sole responsibility for the handling and disposition of such recall, market withdrawal or correction. In the event that a recall is required in connection with BI Austria’s breach of any of its warranties set forth in Section 9.2 hereof, BI Austria shall reimburse InterMune for the purchase price of such PRODUCT and all other reasonable costs and expenses associated with such PRODUCT recall, market withdrawal or correction, but only to the extent that the foregoing costs and expenses are attributable to BI Austria’s breach of its warranties hereunder. In all other events of a recall, all costs and expenses incurred in connection with such PRODUCT recall shall be borne by InterMune. InterMune and/or its designee shall serve as the sole point of contact with the FDA or other applicable HEALTH AUTHORITY concerning any recall, market withdrawal or correction with respect to the PRODUCT.

8.4 Insurance

     During the term of this AGREEMENT, the Parties shall maintain product liability insurance in such amounts and with such scope of coverage as are adequate to cover the Parties’ obligations under this AGREEMENT and as appropriate for companies of like size, taking into account the scope of activities contemplated herein. Notwithstanding the foregoing the Parties shall maintain minimum limits of liability of [*] US$  per occurrence and in the aggregate annually. The Parties shall provide to each other within ten ( 10) business days of execution of this AGREEMENT and thereafter, once a year upon the other Party’s request, a certificate of insurance evidencing the respective Party’s product liability insurance. In addition to the foregoing coverage, the Parties shall maintain Comprehensive General Liability Insurance for limits of not less than [*] US$ combined single limit for bodily injury and broad form property damage.

9. Representations And Warranties

9.1 Each Party hereby represents and warrants to the other Party that: (a) the person executing this AGREEMENT is authorized to execute this AGREEMENT; (b) this AGREEMENT is legal and valid and the obligations binding upon such Party are enforceable by their terms; and (c) the execution, delivery and performance of this AGREEMENT does not conflict with any agreement, instrument or understanding, oral or written, to which such Party may be bound, nor violate any law or regulation of any court, governmental body or administrative or other agency having jurisdiction over it.

9.2 BI Austria represents and warrants that:

     9.2.1 All BBS manufactured hereunder shall conform to BULK SPECIFICATIONS;

     9.2.2 All PRODUCT manufactured and supplied hereunder shall – at the date of shipment - conform to the PRODUCT SPECIFICATIONS;

     9.2.3 All BBS and PRODUCT manufactured and supplied hereunder shall be manufactured in accordance with the MANUFACTURING PROCESS;

     9.2.4 All BBS and PRODUCT manufactured hereunder shall be manufactured, handled, stored, labeled, packaged and transported (from BI Austria to BI Pharma KG) in accordance with the cGMP requirements, the QUALITY ASSURANCE REQUIREMENTS as set forth in the QUALITY AGREEMENT and all applicable laws, regulations and ordinances of the jurisdiction in which such manufacture occurs.

     9.2.5 No PRODUCT manufactured and supplied to InterMune hereunder shall be (i) adulterated or misbranded by BI Austria within the meaning of the FD&C Act, or (ii) an article

that may not be introduced into interstate commerce under the provisions of Sections 404 or 505 of the FD&C Act; and

     9.2.6 BI Austria shall not use and shall secure that BI Pharma KG shall not use in any capacity the services of any persons debarred under 21 U.S.C. sections 335 (a) and 335 (b) in connection with the manufacture of the PRODUCT under this AGREEMENT.

9.3 Except as expressly provided for herein, BI Austria makes no further warranties of the merchantability or fitness of the PRODUCT or any warranties of any other nature, express or implied.

10. Indemnification

10.1 Subject to Section 10.3, BI Austria shall indemnify, defend and hold harmless InterMune and its officers, directors, employees and agents from and against all third party costs, claims, (including death and bodily injury) suits, expenses (including reasonable attorneys’ fees), liabilities and damages (collectively, “LIABILITIES”) arising out of or resulting from any willful or negligent act or omission by BI Austria or BI Pharma KG relating to the subject matter of this AGREEMENT, or any defect in the manufacture or any failure to deliver PRODUCT in accordance with BI Austria’s warranties (except to the extent such LIABILITIES arose or resulted from any negligent act or omission by InterMune).

10.2 Subject to Section 10.3, InterMune shall indemnify, defend and hold harmless BI Austria and its officers, directors, employees and agents from and against all LIABILITIES arising out of or resulting from any willful or negligent act or omission by InterMune relating to the subject matter of this AGREEMENT, or the use by or administration to any person of a PRODUCT that arises out of this AGREEMENT (except to the extent such LIABILITIES arose or resulted from any negligent act or omission by BI Austria or BI Pharma KG or any defect in the manufacture of PRODUCT or any failure to deliver PRODUCT in accordance with BI Austria’s warranties).

10.3 A Party and its directors, officers, employees and agents which intends to claim indemnification under this Article 10 (each, an “INDEMNITEE”) shall promptly notify the other Party (the “INDEMNITOR”) in writing of any action, claim or other matter in respect of which the INDEMNITEE intend to claim such indemnification; provided, however, that the failure to provide such notice within a reasonable period of time shall not relieve the INDEMNITOR of any of its obligations hereunder except to the extent that the INDEMNITOR is prejudiced by such failure. The INDEMNITEE shall permit the INDEMNITOR at its discretion to settle any such action, claim or other matter, and the INDEMNITEE agrees to the complete control of such defense or settlement by the INDEMNITOR. Notwithstanding the foregoing, the INDEMNITOR shall not enter into any settlement that would adversely affect the INDEMNITEE’s rights hereunder, or impose any obligations on the INDEMNITEE in addition to those set forth herein in order for it to exercise such rights, without INDEMNITEE’s prior

written consent, which shall not be unreasonably withheld or delayed. No such action, claim or other matter shall be settled without the prior written consent of the INDEMNITOR, which shall not be unreasonably withheld or delayed. The INDEMNITOR shall not be responsible for any attorneys’ fees or other costs incurred other than as provided herein. The INDEMNITEE shall cooperate fully with the INDEMNITOR and its legal representatives in the investigation and defense of any action, claim or other matter covered by the indemnification obligations of this Article 10. The INDEMNITEE shall have the right, but not the obligation, to be represented in such defense by counsel of its own selection and at its own expense.

11. Limitations On Liability

11.1 In no event shall either Party be liable to the other Party for any consequential, incidental, special or indirect damages arising in connection with this AGREEMENT except in the case of willful misconduct or omission by such Party.

11.2 Except as set forth in the following sentence, BI Austria’s total liability under this Agreement shall not exceed [*]. However, with respect to BI Austria’s indemnification obligations under Article 10, BI Austria’s total liability shall not exceed [*] Euros per occurrence of an act or omission by BI Austria giving rise to a claim for indemnification by InterMune against BI Austria under Article 10, except in the event of BI Austria’s gross negligence or willful misconduct.

12. Confidentiality

12.1 Each Party shall treat confidentially all CONFIDENTIAL INFORMATION of the other Party, and shall not use or disclose such CONFIDENTIAL INFORMATION other than it is expressly permitted under this AGREEMENT. Each Party will take steps to protect the other Party’s CONFIDENTIAL INFORMATION that are at least as stringent as the steps such Party uses to protect its own CONFIDENTIAL INFORMATION, but in no event shall be less than reasonable. Each Party may disclose the other Party’s CONFIDENTIAL INFORMATION to employees, contractors and agents who are bound by written obligations of confidentiality and non-use consistent with those set forth in this AGREEMENT. BI Austria may disclose CONFIDENTIAL INFORMATION for corporate reporting purposes to its AFFILIATES BI Pharma KG and Boehringer Ingelheim GmbH.

12.2 Each Party may disclose Confidential Information of the other Party hereunder to the extent that such disclosure is reasonably necessary for prosecuting or defending litigation, complying with applicable government regulations, conducting preclinical or clinical trials or obtaining marketing approval for the PRODUCT, provided that if a Party is required by law or regulation to make any such disclosure of the other Party’s CONFIDENTIAL INFORMATION it will, except where impracticable for necessary disclosures, for example in the event of medical emergency, give reasonable advance notice to the other Party of such disclosure requirement and

will use its best efforts assist such other Party to secure a protective order or confidential treatment of such CONFIDENTIAL INFORMATION required to be disclosed.

12.3 Neither Party shall disclose CONFIDENTIAL INFORMATION of the other Party in any patent filings without the prior written consent of such other Party.

12.4 The Parties agree that, except as may otherwise be required by applicable laws, regulations, rules, or orders, including without limitation the rules and regulations promulgated by the US Securities and Exchange Commission, and except as may be authorized in Section 12.2, no material information concerning this AGREEMENT and the transactions contemplated herein shall be made public by either Party without the prior written consent of the other. The Parties agree that the public announcement of the execution of this AGREEMENT shall be by one or more press releases mutually agreed to by the Parties. A failure of a Party to return a draft of a press release with its proposed amendments or modifications to such press release to the other Party within five (5) business days of such Party’s receipt of such press release shall be deemed as such Party’s approval of such press release as received by such Party. Each Party agrees that it shall cooperate fully and in a timely manner with the other with respect to all disclosures to the Securities and Exchange Commission and any other governmental and regulatory agencies, including requests for confidential treatment of CONFIDENTIAL INFORMATION of either Party included in any such disclosure.

12.5 This confidentiality obligations of this Article 12 shall survive the termination or expiration of this AGREEMENT for a period of five (5) years.

13. Duration and Termination

13.1 Duration

     The AGREEMENT shall be effective as of the Effective Date and shall continue in force until December 31, 2012. No later than [*] prior to the expiration of this AGREEMENT, the Parties shall discuss and determine whether the term of the AGREEMENT shall be extended by the Parties. In the event the Parties mutually determine that the term of the AGREEMENT should be extended, the Parties shall enter into an amendment to this AGREEMENT to effectuate such an extension.

13.2 Early Termination

     13.2.1 In the event that a Party materially breaches its obligations under this AGREEMENT (including without limitation a MATERIAL SUPPLY BREACH), the non-breaching Party may terminate this AGREEMENT upon thirty (30) days prior written notice to the breaching Party, unless the breaching Party cures such breach to the non-breaching Party’s reasonable satisfaction during such thirty day period. Notwithstanding the preceding sentence, in the event that a Party materially breaches its obligations under this AGREEMENT more than

two (2) times in any consecutive twenty-four (24) month period, the non-breaching Party may terminate this AGREEMENT immediately without providing the breaching Party an opportunity to cure such breach, by giving the breaching Party written notice thereof.

     13.2.2 Each Party may terminate this AGREEMENT by notice in writing to the other Party, for cause, if such other Party is adjudicated to be insolvent or files a petition in bankruptcy.

     13.2.3 InterMune may immediately terminate this AGREEMENT by notice in writing if InterMune should be prevented by the HEALTH AUTHORITIES from distributing PRODUCT on the market for all indications. In such event, [*] for the following: (A) InterMune shall either (at InterMune’s discretion) (i) [*] in accordance with the then existing [*] under the [*] (in which case [*] to InterMune) or (ii) [*] of the unit price of the PRODUCT then in effect for the PRODUCT forecasted in the then existing [*] under the [*]; and (B) InterMune [*] any non-cancelable costs incurred by BI Austria for equipment dedicated to the PRODUCT which equipment was purchased by BI Austria at InterMune’s request to the extent that InterMune has not yet paid for such equipment; provided that InterMune shall have no liability to BI Austria under this Section 13.2.3 in the event that such HEALTH AUTHORITY action is solely due to any breach of BI Austria’s warranties under this Agreement or any negligence or willful misconduct by BI Austria or BI Pharma KG.

     13.2.4 Either Party may terminate this AGREEMENT upon [*] months written notice in the event that the other Party assigns this AGREEMENT pursuant to Section 14.3.

     13.2.5 All payments in connection with early termination shall be due within thirty (30) days after receipt by BI Austria of the notice of early termination from InterMune and receipt by InterMune of the respective invoice from BI Austria.

13.3 Effect of Termination

     13.3.1 In the event of any termination of this AGREEMENT (other than for BI Austria’s material breach or negligence or willful misconduct by BI Austria or BI Pharma KG), InterMune shall also do one of the following (at InterMune’s option): (i) InterMune shall purchase (in which case BI Austria shall sell) PRODUCT forecasted for [*] (i.e., [*]) and for [*] (i.e., [*) of the then existing forecast or (ii) InterMune shall pay to BI Austria an amount equal to [*] of the unit price of the PRODUCT then in effect for the PRODUCT forecasted [*]; provided, however, that with regard to any [*] by BI Austria (or BI Pharma KG, as the case may be) at the time of termination, [*] PRODUCT at [*]. Notwithstanding the foregoing, in the event of termination by InterMune under Section 13.2.3, Section 13.2.3 shall govern rather than this Section 13.3.1.

     13.3.2 In the event of any termination or expiration of this AGREEMENT, at the request of InterMune, BI Austria shall either (i) destroy all material, including but not limited to samples

and all documentation received from InterMune under this AGREEMENT and under the ORIGINAL SUPPLY AGREEMENT, or (ii) deliver the same to InterMune or a party nominated by InterMune, at InterMune’s cost (except in the case of termination by InterMune for BI Austria’s material breach, in which case such destruction or delivery shall be at BI Austria’s expense).

     13.3.3 BI Austria shall promptly return all of InterMune’s CONFIDENTIAL INFORMATION (as well as all CONFIDENTIAL INFORMATION of InterMune provided to BI Austria under the ORIGINAL SUPPLY AGREEMENT) to InterMune, except for a single copy and/or sample of each item for documentation purposes only. BI Austria’s responsibility to keep and store all other materials provided by InterMune in the course of this AGREEMENT shall terminate six (6) months after expiration or termination of this AGREEMENT (except as otherwise provided in Section 5.2).

     13.3.4 InterMune shall promptly return all of BI Austria’s CONFIDENTIAL INFORMATION (as well as all CONFIDENTIAL INFORMATION of BI Austria provided to InterMune under the ORIGINAL SUPPLY AGREEMENT) to BI Austria, except for a single copy and/or sample for documentation purposes only.

     13.3.5 The following provisions shall survive termination of this AGREEMENT: Sections 3.8.1, 5.2.3, 7.1, 7.2, 7.3, 7.4, 7.5, 8, 10, 11, 12, 13.2.3, 13.2.5, 13.3 and 14. Termination of this AGREEMENT shall not relieve either Party of any liability which accrued hereunder prior to the effective date of such termination, nor preclude either Party from pursuing all rights and remedies it may have hereunder or at law or in equity with respect to any breach of this AGREEMENT, nor prejudice either Party’s right to obtain performance of any obligation.

14. Miscellaneous

14.1 Performance by Affiliates

     The Parties recognize that each Party may perform some or all of its obligations under this AGREEMENT through one or more of its AFFILIATES, provided, however, that each Party shall remain responsible for such performance by its AFFILIATES and shall cause its AFFILIATES to comply with the provisions of this AGREEMENT in connection with such performance. Each Party hereby expressly waives any requirement that the other Party exhaust any right, power or remedy, or proceed against an AFFILIATE, for any obligation or performance hereunder prior to proceeding directly against such Party.

14.2 Force Majeure

     Neither Party shall be liable for any failure or delay in performance or non-performance caused by circumstances beyond the reasonable control of such Party, including but not limited to acts of God, explosion, fire, flood, labor strike or labor disturbances, sabotage, order or decree

of any court or action of any governmental authority (except where such order, decree or action is a direct result of BI Austria’s breach of its obligations hereunder), or other causes, whether similar or dissimilar to those specified which cannot reasonably be controlled by the Party who failed to perform (each such event, a “FORCE MAJEURE EVENT”). A Party affected by a FORCE MAJEURE EVENT shall give notice of such to the other Party as soon as is reasonably possible, and shall resume performance hereunder as soon as is reasonably possible. Each Party shall have the right to terminate this AGREEMENT in the event that a FORCE MAJEURE EVENT continues for more than thirty (30) business days upon written notice thereof.

14.3 Assignment

     14.3.1 Except as expressly provided for herein neither this AGREEMENT nor any rights or obligations hereunder may be assigned by either Party except to an AFFILIATE of either one of the Parties without the prior written consent of the other Party which shall not be unreasonably withheld or delayed. Any subsequent assignee or transferee shall be bound by the terms of this AGREEMENT. Any assignment of this AGREEMENT that is not in conformance with this Section 14.3 shall be null, void and of no legal effect.

     14.3.2 Notwithstanding the foregoing, InterMune shall have the right to assign this AGREEMENT in case of a merger, acquisition or sale of substantially all of its assets that relate to this AGREEMENT after due written notification of BI Austria. In the event the InterMune assignee is a direct competitor of BI Austria in the field of contract manufacturing of biopharmaceuticals by means of microbial or yeast fermentation, any document reviews or site inspections (e.g. annual audit) by such assignee as permitted under this AGREEMENT must only be exercised by an independent third party consultant agreed upon between the Parties such that the assignee will not have direct access to BI Austria’s CONFIDENTIAL INFORMATION and such independent third party’s disclosure of BI Austria’s CONFIDENTIAL INFORMATION to such assignee will be limited to the full extent possible in order to protect BI Austria’s CONFIDENTIAL INFORMATION.

     14.3.3 In the event that either Party assigns this AGREEMENT as permitted under this Section, the other Party shall have the right to terminate this AGREEMENT upon [*] months written notice. InterMune shall not have the right to terminate this AGREEMENT under this Section 14.3.3 (i) in the event of assignment of the Agreement by BI Austria to an AFFILIATE existing on the Effective Date in accordance with Section 14.3.1, or (ii) in the event BI Austria assigns the Agreement to an AFFILIATE not in existence on the Effective Date and such assignment would have no impact on the day-to-day operations of BI Austria such that the same facility in [*] would continue to perform its manufacturing obligations under this Agreement.

14.4 Notices

     Any notice required or permitted to be given hereunder by either Party shall be in writing and shall be (i) delivered personally, (ii) sent by registered mail, return receipt requested, postage prepaid or (iii) delivered by facsimile and confirmed by certified or registered mail to the addresses or facsimile numbers set forth below:

If to InterMune:		InterMune, Inc. 3280 Bayshore Boulevard Brisbane, CA 94005 USA Facsimile: +1 – 415 – 466 – 2300 Attention:
With a copy to:		InterMune, Inc. 3280 Bayshore Boulevard Brisbane, CA 94005 USA Facsimile: +1 – 415 – 466 – 2300 Attention: General Counsel
If to BI Austria:		Boehringer Ingelheim Austria GmbH Dr. Boehringer-Gasse 5 – 11 A-1121 Vienna, Republic of Austria Facsimile: +43 – 1 – 801 05 – 2440 Attention: Monika Henninger Customer Relations & Projects
with a copy to:		Boehringer Ingelheim GmbH Binger Strasse 173 D-55 216 Ingelheim am Rhein Facsimile: +49 – 61 32 77 – 98 287 Attention: Rolf G. Werner Corporate Division Biopharmaceuticals

14.5 Dispute Resolution; Governing Law

     14.5.1 In the event of any controversy or claim arising out of, relating to or in connection with any provision of this AGREEMENT, or the rights or obligations of the Parties hereunder, the Parties first shall try to settle their differences amicably between themselves by referring the disputed matter to the Chief Executive Officer of InterMune and the Chief Executive Officer of BI Austria for discussion and resolution. Either Party may initiate such informal dispute resolution by sending written notice of the dispute to the other Party, and within ten (10) days of such notice the Chief Executive Officer of InterMune and the Chief Executive Officer of BI Austria shall meet for attempted resolution by good faith negotiations. If such personnel are

unable to resolve such dispute within thirty (30) days of initiating such negotiations, the controversy or claim will be referred to binding arbitration as set forth in Section 14.5.2.

     14.5.2 Any controversy or claim arising out of, relating to or in connection with any provision of this AGREEMENT, or the rights or obligations of the Parties hereunder, and not resolved by executive mediation in accordance with Section 14.5.1 hereof, shall be referred to and finally settled by binding arbitration, in accordance with the Rules of Arbitration of the International Chamber of Commerce in force on the date the demand for arbitration is filed, which Rules are deemed to be incorporated by reference into this clause. The demand for arbitration may be filed by either Party within a reasonable time after the executive mediation in accordance with Section 14.5.1 has concluded, but no later than after the date upon which institution of legal proceedings shall be barred by the applicable statute of limitations. There shall be three (3) arbitrators. Each Party shall designate one arbitrator and the two party-designated arbitrators shall select the third. In the event of the any one or more of the three (3) arbitrators has not been selected by the thirtieth (30th) day following the date of the demand for arbitration, then such arbitrator shall be selected in accordance with the aforesaid Rules. The language to be used in the arbitral proceedings shall be English. The place of arbitration shall be San Francisco, California, USA in the event InterMune is the defendant and Vienna, Austria in the event BI Austria is the defendant. Any determination by such arbitration shall be final and conclusively binding. Judgment on the arbitral award may be entered in any court having jurisdiction thereof. In the event of arbitration, the costs of the arbitration shall be fixed in accordance with Article 31 of the Rules of Arbitration of the International Chamber of Commerce and the final award will have the Parties bearing the costs of arbitration in proportion to the outcome of the arbitration. If applicable under the applicable law, the Parties will submit a proposed discovery schedule to the arbitrator(s) at the pre-hearing conference. The scope and duration of discovery shall be reasonably determined by the arbitrators.

     14.5.3 This AGREEMENT shall be governed by and construed in accordance with the laws of the place of domicile of the defendant party.

     14.5.4 The Parties expressly exclude the application of the United Nations Convention on Contracts for the International Sale of Goods to this AGREEMENT.

14.6 Independent Contractor

     Each of the Parties hereto is an independent contractor and nothing herein contained shall be deemed to constitute the relationship of partners, joint venture, nor of principal and agent between the Parties hereto. Neither Party shall have the authority to bind the other Party.

14.7 Waiver

     Any delay in enforcing a Party’s rights under this AGREEMENT or any waiver as to a particular default or other matter shall not constitute a waiver of such Party’s rights to the future enforcement of its rights under this AGREEMENT, excepting only as to an express written and signed waiver as to a particular matter for a particular period of time.

14.8 Severability

     If any of the provisions of this AGREEMENT or parts thereof should be or become invalid, the remaining provisions will not be affected. The Parties shall undertake to replace the invalid provision or parts thereof by a new provision which will approximate as closely as possible the intent of the Parties.

14.9 Entire Agreement

     This AGREEMENT, the QUALITY AGREEMENT, the TERMINATION AGREEMENT and the Exhibits set forth the entire agreement between the Parties, and supersede all previous agreements, negotiation and understanding, written or oral, regarding the subject matter hereof. This AGREEMENT may be modified or amended only by an instrument in writing duly executed on behalf of the Parties. For the avoidance of doubt, this AGREEMENT does not supersede the TERMINATION AGREEMENT entered into by the Parties on June 6, 2007.

14.10 Headings

     The section headings appearing herein are included solely for convenience of reference and are not intended to affect the interpretation of any provision of this AGREEMENT.

14.11 Ambiguities

     Ambiguities, if any, in this AGREEMENT shall not be strictly construed against either Party, regardless of which Party is deemed to have drafted the provision at issue.

14.12 Counterparts

     The AGREEMENT may be executed in two or more counterparts, each of which shall be an original and all of which shall constitute the same document.

14.13 English Language

     The English language will govern any interpretation of or dispute in connection with this AGREEMENT.

14.14 Effect on Termination Agreement

     Upon the full execution of this AGREEMENT by all the Parties, the Effective Date of this AGREEMENT shall be deemed the “Termination Date” for purposes of the TERMINATION AGREEMENT.

     In Witness Whereof, the Parties hereto have caused this AGREEMENT to be executed by their duly authorized representatives as of the Effective Date.

Vienna, Austria						Brisbane, California
BOEHRINGER INGELHEIM AUSTRIA GMBH						INTERMUNE, INC.
By:		/s/ Dipl. Vw. Frank Ternes				By:		/s/ Robin Steele
Name:		Dipl. Vw. Frank Ternes				Name:		Robin Steele
Title:		Senior Vice President, Division Biopharmaceuticals & Operations				Title:		Senior Vice President, General Counsel
Date:		29 June 2007				Date:		29 June 2007
By:		/s/ Prof. Dr. Rolf G. Werner
Name:		Prof. Dr. Rolf G. Werner
Title:		Senior Vice President,
		Corporate Division Biopharmaceuticals
Date:		29 June 2007

EXHIBIT 1

BBS SPECIFICATIONS

[*]

EXHIBIT 2

Certificate of Analysis (COA)

[*]

EXHIBIT 3

[*]

EXHIBIT 4

DNA sequence of INTERFERON GAMMA 1b

[*]

EXHIBIT 5

Manufacturing Process

[*]

EXHIBIT 6

Product

[*]

EXHIBIT 7

Project Manager and Project Team

[*]

EXHIBIT 8

Project Specification

[*]

EXHIBIT 9

Steering Committee

[*]