License Agreement

Exhibit 10.12

License Agreement

executed as of the date last below written (hereinafter referred to as “Effective Date”) by and between

XXXXXXX PHARMACEUTICA, Naamloze Vennootschap, a business corporation organized under the laws of Belgium, entered in the Trade Register of Turnhout under Nr. 4203, having its principal office at B-2340 Beerse (Belgium), Turnhoutseweg 30, facsimile: x00 00 000 000 (hereinafter referred to as “XXXXXXX”)

and

Theravance, INC., a businesses corporation organized under the laws of Delaware, United States of America, and having its principal xxxxxx xx Xxxxx Xxx Xxxxxxxxx, XX 00000, 000 Xxxxxxx Xxxxxxxxx, facsimile: x0000-000-0000 (hereinafter referred to as “THERAVANCE”)

WITNESSETH

WHEREAS, XXXXXXX has developed through its research a drug delivery system on the basis of cyclodextrin derivatives for the administration of therapeutic compounds with low aqueous solubility or chemical stability; and

WHEREAS, XXXXXXX has accumulated and is the owner of certain proprietary information in connection with the use of hydroxypropyl-beta-cyclodextrin (“HPBCD”) in pharmaceutical applications; and

WHEREAS, XXXXXXX owns or controls certain patent and/or patent applications in connection with the use of HPBCD in pharmaceutical applications; and

WHEREAS, THERAVANCE intends to use HPBCD in the development and commercialisation of injectable glycopeptide antibiotics for the treatment of gram positive bacteria in humans (e.g., TD-6424), and has requested a license from XXXXXXX under the above-mentioned patents and proprietary information for said purpose; and

WHEREAS, XXXXXXX is willing to grant such a license under the terms and conditions set forth hereinafter.

NOW, THEREFORE, in consideration of the premises, mutual covenants and obligations herein contained, it is agreed by and between the parties hereto as follows

Article 1 :  Definitions

Each term defined below shall, for the purpose of this Agreement, have the following meaning unless the context clearly requires otherwise and the singular shall include the plural and vice versa:

1.1 “Affiliate” of a party to this Agreement shall mean any company which owns or controls at least forty per cent (40%) of the voting stock of such party or any other company at least forty per cent (40%) of whose voting stock is owned by or controlled by such owning or controlling company or by a party to this Agreement.

1.2 “Field” shall mean injectable glycopeptide antibiotics for the treatment of gram positive bacteria in humans.

1.3 “HPBCD” shall mean a selected hydroxypropyl derivative of beta-cyclodextrin for use in pharmaceutical applications, as covered by the Patents, which increases the aqueous solubility of drugs with a low aqueous solubility and/or chemical stability and the toxicological and pharmacokinetic profile of which is specified in the Know How.

1.4 “Know-How” shall mean all scientific and technical data, information and knowledge concerning HPBCD and the use thereof in pharmaceutical applications now or hereafter owned by or under the control of XXXXXXX. Know-How shall include but shall not be limited to pharmaceutical data, the summary of the toxicological studies and specific data on the intravenous route and the summary of metabolism and kinetic studies of HPBCD, all as indicated in Exhibit II hereto and made a part hereof.

1.5 “Major Countries” shall mean any or all of the following: United States, UK, France, Germany, Spain and Italy.

1.6 “Net Sales” shall mean the amount billed, invoiced or received (whichever is first) on first sales of any Product to non-Affiliate third-party customers by THERAVANCE or by any Affiliate or sublicensee of THERAVANCE in the Territory, less:

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(a) Customary trade, quantity, or cash discounts and non-affiliated brokers’ or agents’ commissions actually allowed and taken, discounts, refunds, chargebacks, retroactive price adjustments, rebates, including but not limited to government mandated rebates, and any other allowances which effectively reduce the net selling price;

(b) Amounts repaid or credited by reason of rejections or return; and/or

(c) Any freight or other transportation costs, insurance charges, duties, tariffs and all sales and excise taxes based directly on sales or turnover or delivery or use of material produced under this Agreement and/or

(d) Any other similar and customary deductions (as defined and accepted by generally accepted accounting principles (“GAAP”)), actually incurred.

Net Sales shall not include sales of Product by THERAVANCE to its sub-licensees.

1.7 “Patents” shall mean the patents and patent applications owned or controlled (including patents that can be sublicensed) by XXXXXXX or by any XXXXXXX Affiliate claiming the use of HPBCD in pharmaceutical applications, including any continuations, continuations-in-part, divisions, reissues, renewals or extensions thereof or any supplementary protection certificate granted on the basis of the marketing authorisations obtained by THERAVANCE for the Product. An updated list of the Patents is attached hereto as Exhibit 1.

1.8 “Process Patents” shall mean the patent owned, or licensed by XXXXXXX, as specifically listed in Exhibit B, that claims a process for preparing HPBCD, including any extensions thereof or any supplementary protection certificate relating thereto or any other patent or patent application hereafter acquired by XXXXXXX under which XXXXXXX is licensed with the right to sub-license and which patent or patent applications claimed pertain to the process of manufacturing HPBCD.

1.9 “Product” shall mean any pharmaceutical product in finished dosage form containing TD-6424 and HPBCD for the treatment of multi-drug resistant gram positive infections in humans the manufacture, use or sale of which infringes a Valid Claim of a Patent, and/or, utilises the proprietary information encompassed in the Know-How.

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1.10 “Specifications” shall mean the basic specifications of HPBCD described in Exhibit III hereto and made a part hereof.

1.11 “Territory” shall mean the world.

1.12 “Valid Claim” shall mean a claim in a Patent which has not lapsed or become abandoned and which claim has not been declared invalid or that has not been finally rejected by a court of competent jurisdiction or a patent authority such as the European Patent Office or which has not been admitted to be invalid or unenforceable through reissue or disclaimer.

Article 2 :  Grant

2.1 Subject to the terms and conditions of this Agreement, XXXXXXX hereby grants THERAVANCE a world-wide sole license in the Field under the Patents (i.e. “sole license” means XXXXXXX solely retains the right to practice under the Patents in the Field without the right to transfer, other than to an Affiliate, any rights under the Patents in the Field and THERAVANCE has an exclusive license under the Patents in the Field subject only to XXXXXXX’x retained right) and a world-wide sole license in the Field under the Know-How for the sole purpose of developing, registering, making, having made, using and selling the Products and a non-exclusive license under the Process Patents for the sole purpose of making or having HPBCD made for the benefit of THERAVANCE, THERAVANCE’s Affiliates or THERAVANCE’s sublicensees for the Product in accordance with Article 5 below.

2.2 Promptly following the Effective Date, and thereafter during the term of this Agreement, XXXXXXX shall disclose the Know-How to THERAVANCE or to regulatory agencies as THERAVANCE deems necessary for the exercise of its rights hereunder.

2.3 All rights herein granted, are personal to THERAVANCE and are indivisible and non-transferable, subject to Article 2.4 below, except that the rights granted to THERAVANCE may be exercised by any of THERAVANCE’s Affiliates.

2.4 THERAVANCE will be entitled to grant sublicenses for the Product to third parties. THERAVANCE will notify XXXXXXX of any third party so sublicensed by THERAVANCE. THERAVANCE shall procure that any such third party so sublicensed

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will abide by the obligations of this Agreement. In the event such a sublicense pertains to one or more Major Countries, THERAVANCE shall require Xxxxxxx’x prior written approval, such approval not to be unreasonably withheld.

2.5 THERAVANCE acknowledges XXXXXXX’x representation that, depending on the nature and scope of the responsibilities sublicensed to such a third party in the United States, it may be necessary for XXXXXXX to consult with the Public Health Services Office of Technology (“XXX”) further to an agreement entered into between Xxxxxxx and XXX on March 26, 1998 (“XXX Agreement”).

Article 3 :  Royalties - Milestone payments

3.1 In consideration of the rights and licenses granted by XXXXXXX to THERAVANCE, THERAVANCE agrees to pay a royalty of two and one half percent (2.5%) on Net Sales for the license under the Know-How and a royalty of two and one half percent (2.5%) on Net Sales for the license under the Patents.

3.2 THERAVANCE’s obligation to pay Patent royalties hereunder will remain in effect on a country-by-country basis until expiration of the last Patent in the subject country having a Valid Claim covering the Product.

THERAVANCE’s obligation to pay Know-How royalties shall remain in effect for a period of ten years following the first commercial sale of Product in any country of the Territory. No further Know-How royalties shall be payable after the expiry of the above ten-year period.

Notwithstanding the above, it is understood that the combined Patent and Know-How royalties payable by THERAVANCE shall amount to no less than four percent (4%) on a country-by-country basis for a period of five years following first commercial sale of the Product notwithstanding the prior expiry of the last Patent in the subject country having a Valid Claim covering the Product.

3.3 In consideration of the rights and licenses granted hereunder, THERAVANCE agrees to pay milestone payments to XXXXXXX in accordance with the following schedule:

· US$ 200,000 shall be paid within thirty (30) days following the execution of this Agreement;

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· US$ 300,000 shall be paid within thirty (30) days following the first filing by THERAVANCE of a marketing authorisation application in relation to the Product;

· US$ 300,000 shall be paid within thirty (30) days following the approval of a marketing authorisation application in relation to the Product granted to THERAVANCE, any of its Affiliates or sub-licensee in the United States;

· US$ 200,000 shall be paid within thirty (30) days following approval of the first marketing authorisation of the Product in the European Union.

The foregoing milestone payments are non-refundable and not creditable against future royalties. In the event that the Product fails at any stage prior to any of the above milestone payments becoming due, such remaining milestone payments shall be payable if the failed Product is replaced by THERAVANCE with a back-up compound in the Field which requires HPBCD for its development and/or commercialisation.

Article 4 :  Sales and Royalty Reports - Royalty Payments

4.1 Ninety (90) days following each calendar quarter, THERAVANCE shall submit to XXXXXXX a sales report showing its total sales of Product in Territory in units and Net Sales value. Such sales report shall also include a royalty report containing a calculation of the royalty due and payable to XXXXXXX.

4.2 Together with such royalty report, THERAVANCE shall pay the royalty due and payable. All royalty payments to be made by THERAVANCE to XXXXXXX shall be converted into US Dollars at the average rate of exchange for the calendar quarter for which royalty payments are being remitted according to THERAVANCE’s normal procedures, as consistently applied by THERAVANCE for its other products.

All payments shall be made by wire transfer to a designated XXXXXXX account within ninety (90) days following the end of each calendar quarter. In the event that royalties are payable with respect to Net Sales in a country whose currency cannot be freely converted, such currency shall be converted in accordance with the normal procedures consistently applied by THERAVANCE

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4.3 Any income or other taxes which THERAVANCE is required by law to pay or withhold on behalf of XXXXXXX with respect to milestones or royalties payable to XXXXXXX under this Agreement shall be deducted from the amount due. THERAVANCE shall furnish XXXXXXX with proof of such payments. Any such tax required to be paid or withheld shall be an expense of and borne solely by XXXXXXX. THERAVANCE shall provide XXXXXXX with a certificate or other documentary evidence to enable XXXXXXX to support a claim for a refund or a foreign tax credit with respect to any such tax so withheld or deducted by THERAVANCE.

4.4 THERAVANCE shall keep true and accurate books clearly specifying its sales per country of Territory in Net Sales value as well as in units sold for the purpose of making such reports.

XXXXXXX shall have the right to nominate an independent certified public accountant acceptable to and approved by THERAVANCE who shall have access, on reasonable notice, to THERAVANCE and its Affiliates’ records during reasonable business hours for the purpose of verifying the royalties payable as provided in this Agreement for the two preceding years. This right may not be exercised more than once in any calendar year, and once a calendar year is audited it may not be re-audited. The said accountant shall disclose to XXXXXXX only information for the purpose of verifying the accuracy of the royalty report and the royalty payments made according to this Agreement.

Any adjustment required by such audit shall be made within thirty (30) days of the determination by the accountants. If the adjustment payable to XXXXXXX is greater than five percent (5%) of the amount paid for the calendar year, then the cost to XXXXXXX for the audit shall be paid by THERAVANCE.

Article 5 :  Supply of HPBCD

5.1 In order to be assured of a source being able to supply constant standard quality of pharmaceutical grade HPBCD complying with the Specifications and the toxicological and pharmacokinetic data contained in XXXXXXX’x Know-How, XXXXXXX has entered into an agreement with ROQUETTE FRERES a manufacturer of cyclodextrins which agreement provides that HPBCD produced by ROQUETTE FRERES shall comply with the Specifications. The data contained within the XXXXXXX Know-How have been validated utilising HPBCD supplied by the said supplier.

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5.2 It will be the responsibility of THERAVANCE to procure supplies of HPBCD either from ROQUETTE FRERES or from an alternative supplier under terms and conditions to be agreed separately with such supplier, provided that, at THERAVANCE’s request, XXXXXXX shall assist THERAVANCE in its negotiations with ROQUETTE FRERES regarding the terms and conditions of supply of HPBCD. If despite good faith efforts ROQUETTES FRERES and THERAVANCE would be unable to enter into a supply agreement, THERAVANCE and XXXXXXX will meet following THERAVANCE’s request to discuss in good faith potential course of action, including the use of alternative suppliers. It is understood by THERAVANCE that to the extent it wants to utilise an alternative supplier, XXXXXXX can not provide a guarantee that such supplier is capable of supplying pharmaceutical grade HPBCD nor that the specifications of such alternative supplier would comply with the data contained within the XXXXXXX Know-How.

Article 6 :  Warranties

6.1 XXXXXXX represents and warrants to the best of its knowledge, that as of the date hereof it has title to and ownership of the Patents and Know-How.

6.2 XXXXXXX makes no representation or warranty, express or implied, that the use of HPBCD shall eventually result in marketable Product. No further statement of warranty covering HPBCD shall be binding on XXXXXXX without the written consent of an authorised officer of XXXXXXX.

6.3 Each party further warrants that it has the right to enter into this Agreement and that it is under no obligation to any third party, express or implied, conflicting with the terms and conditions of this Agreement.

6.4 Nothing in this Agreement shall be considered as a warranty, either express or implied, that the use of HPBCD in Products will not infringe any third party’s patent rights.

Article 7 :  Product liability

7.1 THERAVANCE agrees to indemnify and hold XXXXXXX harmless from and against all claims, actions, direct damages, losses, costs and expenses of any kind resulting from or arising out of claims by third parties based on product liability or similar theories

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relating to the development, manufacturing, transportation, storage, promotion or sale of the Product, except to the extent such losses arose or resulted from faulty conduct or negligence by XXXXXXX in supplying the Know-How and so long as (i) XXXXXXX allows THERAVANCE to participate in or, at THERAVANCE’s sole option but without any obligation, to conduct at THERAVANCE’s expense the defense of a claim or action for which indemnification is sought under this Article, and (ii) XXXXXXX does not compromise or settle such claim or action without THERAVANCE’s prior written consent, which shall not be unreasonably withheld.

7.2 In no event shall THERAVANCE be liable for any consequential or indirect damage of XXXXXXX whatsoever.

Article 8 :  Patent Infringement

8.1 If either party learns of an infringement of a Patent by a third party, using HPBCD in the promotion or sale of a product substantially similar to a Product, the party learning of the alleged infringement shall promptly inform the other party.

8.1.1 In case of such an infringement, XXXXXXX shall have the right (but not the obligation), in its own name and at its own cost, to either bring an enforcement action to stop the alleged infringement or settle with the alleged infringer; provided, however, that no such settlement shall diminish or otherwise affect THERAVANCE’s rights hereunder, unless THERAVANCE gives its prior written consent. THERAVANCE will give reasonable assistance to XXXXXXX in such action against a third party, including making available to XXXXXXX records, information and evidence relevant to the infringement and, if necessary, being named a party in such action.

All sums awarded or received in settlement of such suit shall be equally divided between XXXXXXX and THERAVANCE, after having reimbursed both parties for all reasonable out of pocket expenses incurred in bringing or assisting in such action.

8.1.2 Whenever XXXXXXX elects not to take action against such infringement within a reasonable period of time not to exceed three (3) months THERAVANCE will have the right but not the obligation to take action in its own name, at its own expense and by counsel of its own choice.

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XXXXXXX will give all reasonable assistance in taking such action, including being a named party and making available to THERAVANCE records, information and evidence relevant to the infringement. THERAVANCE will be entitled to all recovery monies awarded or received in settlement of such suit. Any out of pocket expenses incurred by XXXXXXX in assisting THERAVANCE in such action will be reimbursed by THERAVANCE out of the recovery monies awarded or received.

Whenever THERAVANCE so elects to take action XXXXXXX will at any time be entitled to be represented in such action at its own cost and by counsel of its own choice.

THERAVANCE will in no event settle or consent to a judgement or other final disposition of a suit without the prior written approval of XXXXXXX, which shall not unreasonably be withheld. Furthermore, whenever during such action, the infringing party would invoke a declaration of invalidity of the Patents, XXXXXXX will be entitled to take over the direction of the suit.

8.1.3 In the event that all of the claims included within the Patents under which THERAVANCE is developing, registering, or selling the Product shall be held invalid or not infringed by a court of competent jurisdiction, whether or not there is a conflicting decision by another court of jurisdiction, THERAVANCE may pay the royalties which would have otherwise been due under the Patent on sales covered by such claims into an escrow account until such judgement shall be finally reversed by an unappealed or unappealable decree of a court of competent jurisdiction of higher authority, in which event royalty payments shall be resumed and the full amount in escrow shall become due and payable. In the event the judgement is upheld, the full escrow amount will revert to THERAVANCE and no further royalties under the Patents will be due.

8.2 THERAVANCE shall be responsible at its own cost and responsibility to defend against any claim or allegation that the development, manufacturing or commercialisation of the Product infringes a third party patent.

Article 9 :  Regulatory Matters

9.1 THERAVANCE shall be responsible at its own cost to file and maintain the marketing authorisation applications in connection with Product and in general to procure any license, registration or approval required to use HPBCD in the import, manufacture and

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sale of the Product in any country of Territory where THERAVANCE decides to commercialise Product.

All scientific and technical data, information and knowledge developed by THERAVANCE with respect to the Product, including the registration file shall be exclusively owned by THERAVANCE and XXXXXXX shall have no right to use such THERAVANCE’s information.

9.2 XXXXXXX shall reasonably assist THERAVANCE whenever the regulatory authorities in any country of the Territory have questions in relation to HPBCD and the use thereof in pharmaceutical applications. Any request for additional information specifically related to HPBCD shall be referred to XXXXXXX and XXXXXXX shall use reasonable efforts to address the same in due time in consultation with THERAVANCE. To the extent necessary representatives of both parties will meet to discuss any such requests.

Article 10 :  Adverse Drug Reporting

Each party will notify the other in writing of any adverse drug reaction or other unusual physiochemical, pharmacologic, toxicological or pharmacokinetic finding in relation to the use of HPBCD in the Product including, without limitation, any experimental or clinical use. The parties will establish a standard operating procedure in relation to ADE-reporting.

Article 11 :  Commercialisation

All business decisions, including but not limited to the selection of the trademark(s) for Product, pricing, reimbursement, package design, sales and promotional activities and the decision to launch or continue to market a Product in a particular country in the Territory, shall be within the sole discretion and responsibility of THERAVANCE.

Notwithstanding the above it is agreed that THERAVANCE shall otherwise use reasonable efforts consistent with its normal business practices to market and promote Product. In doing so it will use the same level of effort as with its other, similar products of similar sales potential. Failure to use reasonable efforts as qualified herein can be considered a material breach in accordance with the provisions of Article 14.1.

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Article 12 :  Confidentiality - Limitations on Use

12.1 Neither party shall disclose proprietary or confidential information of the other party to any third party without prior written consent of the other party, except and to the extent as required by law, including without limitation to governmental regulatory agencies, and is thereafter publicly disclosed or made available to the public by operation of law, or except that any of such confidential and proprietary information can be shown by the receiving party’s written records:

(i) to be in its possession or in the possession of its employees prior to such disclosure to the receiving party; or

(ii) is now or hereafter becomes available as public knowledge or literature through no fault of the receiving party; or

(iii) is received by such party from an independent third party who did not receive the information directly or indirectly from the other party.

Such proprietary and confidential information shall be disclosed to each party’s personnel only on a strict need-to-know basis.

The obligation of confidentiality contained in this Article, shall survive the expiration and/or termination of this Agreement for five (5) years.

12.2 In the event that THERAVANCE licenses the Product to third parties or otherwise involves third parties in the manufacturing and/or commercialisation of Product and such third party needs to receive certain Know-How, THERAVANCE shall, prior to disclosing any such Know-How enter into a confidentiality undertaking that is essentially similar to the one contained herein and shall in any event provide such Know-How on a strict need-to-know basis.

Article 13 :  Term

Unless sooner terminated in accordance with the provisions of Article 14, this Agreement shall remain in full force and effect from the Effective Date until the date THERAVANCE has no further royalty obligation towards XXXXXXX under the provisions of Article 3.

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Upon termination of THERAVANCE’s royalty obligations for Know-How, THERAVANCE will have a royalty-free right to use the Know-How in the manufacture, use and sale of Product.

Article 14 :  Termination

14.1 In the event XXXXXXX or THERAVANCE or their respective Affiliates (or licensees or distributors in case of THERAVANCE) are in breach of any of the respective obligations and conditions contained in this Agreement the other party shall be entitled to give the party in breach notice requiring it to make good such breach. If such breach constitutes a material breach and is not cured or there is no commencement of cure within sixty (60) days after receipt of such notice, including good faith efforts by senior management of both parties to overcome the issue, the notifying party shall be entitled (without prejudice to any of its other rights conferred on it by this Agreement) to terminate this Agreement by giving a notice to take effect immediately. The right of either party to terminate this Agreement in accordance with this Article 14.1 shall not be affected in any way by its waiver of, or failure to take action with respect to any previous breach.

14.2 In the event that one of the parties hereto shall go into liquidation, a receiver or a trustee be appointed over a significant and/or material property or estate of that party and said receiver or trustee is not removed within sixty (60) days, or the party makes an assignment for the benefit of creditors, and whether any of the aforesaid events be the outcome of the voluntary act of that party, or otherwise, the other party shall be entitled to terminate this Agreement forthwith by giving a written notice to the first party.

14.3 THERAVANCE may terminate this Agreement in its entirety upon one (1) month written notice to XXXXXXX.

Article 15 :  Effects of Termination

In case of termination of this Agreement in accordance with Article 14 and if there is no good faith dispute between the parties, THERAVANCE shall immediately refrain from formulating and selling or offering for sale Product in Territory and return all proprietary and confidential Know-How and information relative to HPBCD together with all physical embodiments thereof shall be returned to XXXXXXX. Furthermore THERAVANCE shall make all payments accrued under this Agreement prior to the effective termination date

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Notwithstanding the above, THERAVANCE may reasonably sell out its remaining stock of Product which THERAVANCE has in stock at the moment of termination of this Agreement, provided it shall pay the royalties due and payable on such sales.

Article 16 :  Force Majeure

Neither party hereto shall be liable to the other party for failure or delay in meeting any obligation hereunder due to circumstances beyond such party’s reasonable control such as, but not limited to, strikes, lockouts, acts of God, riots, war, fire, flood, embargoes, failure of power, acts of government or of any agency, provided that the party affected shall immediately inform the other party about the cause of such delay. The party so affected shall use its reasonable efforts to eliminate, cure and overcome any such causes and resume performance of its covenants with all possible speed.

Article 17 :  Severability

If any clause or provision of this Agreement or the application of any such clause or provision in a particular context or to a particular situation or circumstance should be held unenforceable or otherwise in conflict with or in violation of any applicable law, by, or as a result of determination of any court, tribunal or authority acting in a judicial capacity of competent jurisdiction, the decision of which is binding upon the parties, the parties agree that such determination shall not affect the validity and application of such clause or provision in contexts, situations or circumstances other than that in or to which it is held unenforceable and shall only apply for those countries of the Territory amenable under the law applied by such tribunal, court or authority.

Parties further agree to replace any clause or provision so held unenforceable in a lawful manner, reflecting to the extent possible, the economic, business and other purposes of the clause or provision held void or unenforceable in such specific contexts, situations or circumstances.

Article 18 :  General provisions

18.1 No damages shall be owed by either party to the other if this Agreement or any part of it is held invalid or void at any time by virtue of future acts of legislation.

18.2 Neither party shall assign or otherwise dispose of the whole or any part of its rights under this Agreement without the prior written consent of the other party, except that

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either party may assign this Agreement to one of its Affiliates and except as provided in 18.5.

18.3 Neither party nor its employees or representatives are under any circumstances to be considered as employees or agents or representatives of the other party. Neither party nor its employees have the authority or power to bind the other party or contract in the other party’s name.

18.4 Save as required by law, no announcement or circular in connection with the subject matter of this Agreement shall be made by or on behalf of XXXXXXX or THERAVANCE without the prior approval of the other party, such approval not to be unreasonably withheld. This Agreement may be filed with regulatory authorities as required by law.

18.5 A change of control of THERAVANCE through a merger, acquisition or sale of substantially all assets (including the assets relating to the development of the Product) shall not by and of itself give rise to the right for XXXXXXX to terminate the License, provided always that prior to the closing of any such transaction the acquiring party has agreed in writing to abide by the terms and conditions of the License Agreement.

18.6 No rights are granted by either party to the other except those expressly set forth in this Agreement.

Article 19 :  Dispute Resolution - Applicable Law

The Parties hereto shall attempt to settle any dispute arising out of or relating to this Agreement in an amicable way. In the event that such attempts should fail, then the Parties can take such actions as are available at law under the laws of the State of New York, United States of America, with venue for any such dispute being New York City, New York..

Article 20 :  Notices

Any notice required or permitted under this Agreement shall be made in writing either by registered mail or facsimile to the parties at their respective addresses first above written or as subsequently changed by notice duly given.

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Notices by registered mail are deemed to be given after three (3) days of mailing. Notices by facsimile shall be deemed to be given one day after the date on which such notice has been given.

Article 21 :  Headings

The section headings in this Agreement are for convenience only and shall not in any way affect the meaning or interpretation of this Agreement.

IN WITNESS WHEREOF, XXXXXXX and THERAVANCE have caused this instrument to be executed in duplicate by their respective duly authorised officers.

				THERAVANCE, INC.
				This 14th day of May, 2002
	/s/ Xxxx Xxxxxx			By	/s/ Xxxxx Xxxxxxxx
(title)	Xxxx Xxxxxx			(title)	Xxxxx Xxxxxxxx
	Senior Vice President				Senior Vice President
	General Counsel				Commercial Development
				XXXXXXX PHARMACEUTICA N.V.
				This 14th day of May 2002
/s/ Xxx Xxxxxxx				/s/ Xxx Xxxxxxxxxxx
Xxx Xxxxxxx				Xxx Xxxxxxxxxxx
Licensing Director				International Vice President,
				Business Development

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EXHIBIT I

PATENTS

SCHEDULE A

Hydroxypropyl-β-cyclodextrin patents (Xxxxxx)

“PHARMACEUTICAL COMPOSITIONS CONTAINING DRUGS WHICH ARE INSTABLE OR SPARINGLY SOLUBLE IN WATER AND METHODS FOR THEIR PREPARATION”

Country

Type

Application Number

Filing Date

Patent Number

Grant Date

Expiry Date

Abandonment Date

Australia

PCT

38352/85

20-Dec-84

565966

18-Jan-88

20-Dec-04

Bahrain

REG

BP980

06-Apr-94

10-Mar-08

Bermuda

REG

91

15-Feb-94

20-Dec-04

Canada

470876

21-Dec-84

1222697

09-Jun-87

09-Jun-04

Cyprus (Greek)

REG

1689

27-Jan-93

1689

00-Xxx-00

00-Xxx-00

Xxxxxxx

PCT

3595/85

20-Dec-84

20-Dec-04

EPO

84115965

20-Dec-84

149197

00-Xxx-00

00-Xxx-00

Xxxxxxx

EPO

84115965

20-Dec-84

149197

00-Xxx-00

00-Xxx-00

Xxxxxxx

EPO

84115965

20-Dec-84

149197

00-Xxx-00

00-Xxx-00

Xxxxxx

EPO

84115965

20-Dec-84

149197

00-Xxx-00

00-Xxx-00

Xxxxxxx

EPO

84115965

20-Dec-84

149197

21-Mar-90

20-Dec-04

Great Britain

EPO

84115965

20-Dec-84

149197

00-Xxx-00

00-Xxx-00

Xxxxx

EPO

84115965

20-Dec-84

149197

00-Xxx-00

00-Xxx-00

Xxxxxxxxx

EPO

84115965

20-Dec-84

149197

00-Xxx-00

00-Xxx-00

Xxxxxxxxxxx

EPO

84115965

20-Dec-84

149197

00-Xxx-00

00-Xxx-00

Xxxxxx

EPO

84115965

20-Dec-84

149197

00-Xxx-00

00-Xxx-00

Xxxxxxxxxxx

EPO

84115965

20-Dec-84

149197

00-Xxx-00

00-Xxx-00

Xxxxxxx

PCT

85/3198

20-Dec-84

86140

27-Jul-92

20-Dec-04

Hong Kong

REG

1312/1993

00-Xxx-00

00-Xxx-00

Xxxxxxx

PCT

795/85

20-Dec-84

200943

00-Xxx-00

00-Xxx-00

Xxxxx

PCT

500307/85

20-Dec-84

1852300

21-Jun-94

20-Dec-04

Korea S.

PCT

85-700172

20-Dec-84

59912

00-Xxx-00

00-Xxx-00

Xxxxxx

PCT

853070

20-Dec-84

171888

19-May-93

20-Dec-04

PCT

PCT/EP84/00417

20-Dec-84

Singapore

REG

248/93

16-Jun-93

20-Dec-04

South Africa

84/10042

21-Dec-84

84/10042

25-Sep-85

21-Dec-04

Tanganyika

REG

2465

00-Xxx-00

00-Xxx-00

Xxxxxxxx & Xxxxxx

REG

17/1993

16-Mar-93

20-Dec-04

USA

PCT

06/756498

20-Dec-84

02-Nov-88

USA

CONT

07/264726

31-Oct-88

Zanzibar

REG

P8/1993

22-Apr-94

20-Dec-04

Schedule B

Patents re the manufacture of hydroxypropyl-β-cyclodextrin

“REGIOSELECTIVE SUBSTITUTIONS IN CYCLODEXTRINS”

Country

Type

Application Number

Filing Date

Patent Number

Grant Date

Expiry Date

Abandonment Date

Australia

PCT

53587/90

30-Mar-1990

631628

26-Mar-1993

30-Mar-2010

Canada

PCT

2047726-1

30-Mar-1990

2047726

17-Apr-2001

30-Mar-2010

EPO

PCT

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

30-Mar-2010

Great Britain

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxxxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxxxxxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

00-Xxx-0000

Xxxxxxxxxxx

EPO

90905461.1

30-Mar-1990

465535

3-Jun-1998

30-Mar-2010

Finland

PCT

914620

30-Mar-1990

101385

15-Jun-1998

30-Mar-2010

Hong Kong

98109960

18-Aug-1998

HK100935

28-May-1999

30-Mar-2010

Xxxxxxx

XXX

0000/00

00-Xxx-0000

00-Xxx-0000

Xxxxx

PCT

505324/90

30-Mar-1990

2792610

19-Jun-1998

30-Mar-2010

Korea S.

PCT

91-701230

30-Mar-1990

163440

7-Sep-1998

7-Sep-2013

Norway

PCT

19913871

30-Mar-1990

304269

23-Nov-1998

30-Mar-2010

PCT

PCT/EP90/00524

30-Mar-1990

3-Oct-1991

XXX

000000

17-Dec-1990

5096893

17-Mar-1992

3-Apr-2009

USA

PARENT

332606

3-Apr-1989

3-Apr-1990

18

EXHIBIT II

KNOW-HOW TO BE PROVIDED UPON THE EFFECTIVE DATE

·              Pharmaceutical data

· Physical, chemical and microbiological specifications + analysis methodology and validation

· Reference substance sample

· Production method with specification of solvents used

· Quality of the starting materials used for the production and controls during production

· Evidence of Chemical Structure:

· Physical and chemical data (solubility,...)

· Impurities (related impurities -residual solvents - inorganic impurities...):

·              Nature

·              Control method and validation

·              Limits

· Summary of toxicological studies on the intravenous route.

· Summary of metabolism and kinetic studies of Encapsin

· Access to the Drug Master File and/or similar regulatory documents on a need-to-know basis in connection with TD-6424

19

EXHIBIT III

SPECIFICATIONS

Test description		Specifications		Method
Appearance		White to almost white powder		Visual inspection.
Identity by IR spectroscopy		Complies with reference spectrum		Ph Eur
Identity by Xxxxxxx’x reagent tests: Determination 1 Determination 2		1. The solution keeps clear and blue 2. A xxxxxxx-xxxxx precipitate is formed		E/ID/0006/01
Assay β-cyclodextrin		≤ 1.0 %		HPLC, E/A/0001/01
Relative complexation capacity		85% - 110%		UV absorbance
Molar substitution degree		0.58-0.73		IR spectroscopy
Light absorbing impurities		< 0.5 at 230 - 400 nm		UV absorbance, E/S/7005/01
Appearance of solution 10% w/v aq.		Clear and colourless		Ph Eur
pH		5.0-7.5		E/PH/0001/01
Loss on drying		≤ 5.0 %		Ph Eur
Sulphated ash		≤ 0.2 %		Ph Eur
Reducing Substances		≤ 1.0 %		β-cyclodextrin titration, USP
Heavy metals		≤ 10 ppm		Limit test, Ph Eur
Specific optical rotation		+138° - +144°-		Ph Eur
Total viable aerobic count: Bacteria Fungi and yeasts		≤100 CFU/g of product ≤100 CFUI of product		USP
Pathogens: Salmonella sp. Escherichia coli Staphylococcus aureus Pseudomonas aeruginosa		absent in 10 g of product absent in 10 g of product absent in 10 g of product absent in 10 g of product		USP
Bacterial endotoxins		< 25 EU/g		LAL, Ph. Eur.
Residual solvent: 1,2-propanediol		≤ 5000 ppm		GC
Propylene oxide (if tested)		≤1 ppm		CGC

20