|
Exhibit 10.1
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION. ASTERISKS
(*)
DENOTE SUCH OMISSIONS.
EXECUTION VERSION
ASSET PURCHASE AGREEMENT
by and between
PRAECIS PHARMACEUTICALS INCORPORATED
as Seller,
and
SPECIALITY EUROPEAN PHARMA LIMITED
as Buyer
Dated as of January 29, 2007
TABLE OF CONTENTS
ARTICLE I
DEFINITIONS
ARTICLE II
ASSET PURCHASE
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Section 2.1
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Purchase and Sale of Assets; Assumption of
Liabilities
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10
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Section 2.2
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Purchase Price and Related Matters
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15
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Section 2.3
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Closing
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17
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Section 2.4
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Additional Consideration; Mechanics
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18
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Section 2.5
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Reimbursement for Certain Minimum Annual
Commitment Payments
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20
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Section 2.6
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Further Assurances
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21
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ARTICLE III
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REPRESENTATIONS AND WARRANTIES OF
SELLER
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21
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Section 3.1
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Organization, Qualification and Corporate
Power
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22
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Section 3.2
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Authority
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22
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Section 3.3
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Consents and Approvals;
Noncontravention
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23
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Section 3.4
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Assigned Contracts
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24
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Section 3.5
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Closing Product Materials
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24
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Section 3.6
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Title to Acquired Assets
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25
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Section 3.7
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Intellectual Property
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26
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Section 3.8
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Brokers’ Fees
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26
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Section 3.9
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Litigation
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26
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Section 3.10
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Compliance with Laws; Governmental
Approvals
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26
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Section 3.11
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PRAECIS Europe
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26
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Section 3.12
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Reliance on Representations and
Warranties
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27
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Section 3.13
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No Other Representations or Warranties
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27
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ARTICLE IV
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REPRESENTATIONS AND WARRANTIES OF
BUYER
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Section 4.1
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Organization
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27
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Section 4.2
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Authority
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27
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Section 4.3
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Noncontravention
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28
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CONFIDENTIAL INFORMATION
OMITTED AND FILED SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
i
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Section 4.4
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Brokers’ Fees
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28
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Section 4.5
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Reliance on Representations and
Warranties
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29
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Section 4.6
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No Other Representations or Warranties
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29
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ARTICLE V
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INDEMNIFICATION
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Section 5.1
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Indemnification by Seller
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29
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Section 5.2
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Indemnification by Buyer
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29
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Section 5.3
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Claims for Indemnification
|
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30
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Section 5.4
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Survival
|
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32
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Section 5.5
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Limitations
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32
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Section 5.6
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Treatment of Indemnification Payments
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33
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ARTICLE VI
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ADDITIONAL COVENANTS
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Section 6.1
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Access to Information; Record Retention;
Cooperation
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33
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Section 6.2
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Collection of Accounts Receivable
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36
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Section 6.3
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Restrictive Covenants
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36
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Section 6.4
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Complaints; Recalls
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36
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Section 6.5
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Post-Closing Matters
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37
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Section 6.6
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Tax Matters
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37
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ARTICLE VII
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MISCELLANEOUS
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Section 7.1
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Press Releases and Announcements
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37
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Section 7.2
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No Third Party Beneficiaries
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38
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Section 7.3
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Entire Agreement
|
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38
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Section 7.4
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Succession and Assignment
|
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38
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Section 7.5
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Notices
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38
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Section 7.6
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Amendments and Waivers
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40
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Section 7.7
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Severability
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40
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Section 7.8
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Expenses
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40
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Section 7.9
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Governing Law
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40
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Section 7.10
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Submission to Jurisdiction
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41
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Section 7.11
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Construction
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41
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Section 7.12
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WAIVER OF JURY TRIAL
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41
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Section 7.13
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Exhibits and Schedules
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42
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Section 7.14
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Counterparts and Facsimile Signature
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42
|
CONFIDENTIAL INFORMATION
OMITTED AND FILED SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
ii
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Section 7.15
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Transfer and Sales Tax
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42
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Section 7.16
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Bulk Transfer Laws
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43
|
CONFIDENTIAL INFORMATION
OMITTED AND FILED SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
iii
SCHEDULES (as set forth in the Disclosure
Schedule)
|
Schedule 1.1(a)(iii)
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Certain Assigned Contracts
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Schedule 1.1(b)
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Designated Intellectual Property
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Schedule 1.1(c)
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Manufacturing Contracts
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Schedule 1.1(d)
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Minimum Annual Commitment Payments
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Schedule 1.1(e)
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Registrations
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Schedule 1.1(f)
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Rel-Ease™ Patents
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Schedule 1.1(g)
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PRAECIS Europe Shares
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Schedule 1.1(h)
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Closing Product Materials
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Schedule 2.1(b)(v)
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Excluded Assets
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Schedule 3.3(a)
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Governmental Consents
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Schedule 3.3(b)
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Third Party Consents
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Schedule 3.3(c)
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Conflicts
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Schedule 3.4
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Contracts
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Schedule 3.6
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Schedule 3.7(a)
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Termination and Settlement Agreements
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Schedule 3.7(b)
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Abarelix License
|
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Schedule 3.11
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PRAECIS Europe Contracts
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EXHIBITS
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Exhibit A
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Form of Rel-Ease™ License
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Exhibit B-1
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NDA Transfer Letter
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Exhibit B-2
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IND 51,710 Transfer Letter
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Exhibit B-3
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IND 56,259 Transfer Letter
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Exhibit B-4
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IND 68,939 Transfer Letter
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Exhibit C-1
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NDA Assumption Letter
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Exhibit C-2
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IND 51,710 Assumption Letter
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Exhibit C-3
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IND 56,259 Assumption Letter
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Exhibit C-4
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IND 68,939 Assumption Letter
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Exhibit D
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Bill of Sale
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Exhibit E
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Assignment of Intellectual Property
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Exhibit F
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Assumption Agreement
|
CONFIDENTIAL INFORMATION
OMITTED AND FILED SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
iv
THIS ASSET PURCHASE AGREEMENT (as may be amended,
modified, or supplemented from time to time as provided herein,
this " Agreement ") is made as of the 29th day of January,
2007, by and between PRAECIS PHARMACEUTICALS INCORPORATED, a
Delaware corporation (" Seller ") and SPECIALITY EUROPEAN
PHARMA LIMITED, a companyorganized under the laws of England and
Wales (" Buyer "). Seller and Buyer are referred to
collectively herein as the "Parties" and each, individually as a
"Party."
W I T N E
S S E T H :
WHEREAS, Buyer wishes to purchase from Seller, and Seller wishes
to sell to Buyer, all of Seller’s right, title and interest
in and to the Acquired Assets (as defined below), upon the terms
and subject to the conditions set forth herein; and
WHEREAS, Buyer has agreed to assume the Assumed Liabilities (as
defined below), upon the terms and subject to the conditions set
forth herein;
NOW, THEREFORE, in consideration of the premises, covenants,
representations and warranties contained herein, and for other good
and valuable consideration, the receipt and sufficiency of which
are hereby acknowledged, the Parties, intending to be legally
bound, agree as follows:
ARTICLE I
DEFINITIONS
Whenever used in this Agreement, the terms defined below shall
have the respective indicated meanings:
"Abarelix License" means Seller’s license agreement dated
as of October 17, 1996, as amended as of June 3, 1998, with Indiana
University Foundation (or its assignees) relating to the Indiana
University Intellectual Property.
"Abarelix Product" means (i) abarelix for injectable suspension
and (ii) any other product in whatever form covered by the Abarelix
License.
"Accountant" has the meaning set forth in Section 2.2(b).
"Accounts Receivable" means all accounts receivable, notes
receivable and indebtedness for borrowed money or overdue accounts
receivable, in each case, due and owing from any Third Party.
"Acquired Assets" has the meaning set forth in Section
2.1(a).
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
1
"Acquired Assets MAE" means a material adverse
effect on the Acquired Assets taken as a whole; provided ,
however , that none of the following circumstances, facts or
effects (each an " Effect "), either alone or in
combination, shall be deemed to constitute, nor shall any of the
following be taken into account in determining whether there has
been or will be, an Acquired Assets MAE: (i) any Effect
resulting from Seller’s compliance with the terms of this
Agreement; (ii) any Effect that results from changes or facts or
circumstances affecting the pharmaceutical or biotechnology
industries, or pharmaceutical products for ***************,
generally or (iii) any Effect disclosed in the Disclosure
Schedule.
"Act" means the Federal Food, Drug, and Cosmetic Act, 21 U.S.C.
321, et seq., as amended, and the rules and regulations promulgated
thereunder.
"Additional Abarelix Product" means any Abarelix Product in a
significantly different formulation to that of the Plenaxis
â Product ************************** including any
sustained release or depot formulation.
"Additional Marketing Region" means, collectively, the countries
or territories other than (i) ************** and (ii)
*************************************.
"Agreed Amount" has the meaning set forth in Section 5.3(b).
"Agreement" has the meaning set forth in the first paragraph of
this Agreement.
"Affiliate" means, with respect to any Person, any Person which
directly or indirectly through stock ownership or otherwise either
controls, or is controlled by or under common control with, such
Person.
"Allocation Resolution Period" has the meaning set forth in
Section 2.2(b).
"Ancillary Agreements" has the meaning set forth in Section
2.3(b).
"Assigned Contracts" means, collectively, (i) the Abarelix
License, (ii) the Manufacturing Contracts and (iii) the Contracts
set forth on Schedule 1.1(a)(iii) pursuant to which services
are or have been provided to Seller or PRAECIS Europe with respect
to Plenaxis â Product or the Product Operations; provided ,
however , that "Assigned Contracts" shall not be deemed to
include any Excluded Contracts.
"Assumed Liabilities" has the meaning set forth in Section
2.1(c).
"BfArM" means Bundesinstitut für Arzneimittel und
Medizinprodukte, or any successor agency with substantially the
same responsibility for regulating the development, manufacture and
sale of human pharmaceutical products.
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
2
"Business Day" means any day other than (i) a
Saturday or Sunday or (ii) a day on which banking institutions
located in Boston, Massachusetts are permitted or required by law,
executive order or governmental decree to remain closed.
"Buyer" has the meaning set forth in the first paragraph of this
Agreement.
"Buyer Indemnitees" has the meaning set forth in Section
5.1.
"Buyer Licensed Party" means (i) Affiliates of Buyer and members
of Buyer’s distribution chain for Abarelix Products, and (ii)
any other Third Parties, in each case to which Buyer grants a
license with respect to, or assigns, any of Buyer’s rights
under this Agreement, any Ancillary Agreement or under any of the
Assigned Contracts, or otherwise directly or indirectly sells any
Abarelix Product under any agreement, arrangement or understanding
with Buyer or any Person referred to in clause (i) of this
definition.
"Buyer Licensed Party Consideration" means
****************************.
"Claim Notice" has the meaning set forth in Section 5.3(b).
"Claimed Amount" has the meaning set forth in Section
5.3(b).
"Closing" has the meaning set forth in Section 2.3(a).
"Closing Date" means the date on which the Closing occurs, which
shall be the date of this Agreement.
"Closing Product Inventory" means
********************************.
"Closing Product Materials" means
********************************.
"Code" means the Internal Revenue Code of 1986, as amended.
"Commercially Reasonable Efforts" means
*****************************.
"Confidentiality Agreement" means that certain confidentiality
agreement dated October 4, 2006 between Buyer and Seller.
"Consideration" has the meaning set forth in Section 2.2(b).
"Contracts" means any and all purchase orders, sales orders,
leases, subleases, licenses, indentures, contracts, agreements and
other legally binding arrangements, whether oral or written, in
effect between Seller or PRAECIS Europe, on the one hand, and one
or more Third Parties, on the other hand.
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
3
"Cost Adjusted Sales" means
***************************************.
"Damages" shall have the meaning set forth in Section 5.1.
"Designated Intellectual Property" all patents, patent
applications, domain names, trademarks, service marks, trademark
applications and trade names, including the Trademark Rights, set
forth on Schedule 1.1(b) .
"Development Costs" has the meaning set forth in Section
2.4(b).
"Disclosure Schedule" has the meaning set forth in Article
III.
"Dossier" means the regulatory dossier supporting the Mutual
Recognition Procedure.
"EMEA" means the European Medicines Evaluation Agency, or any
successor agency with substantially the same responsibility for
regulating the development, manufacture and sale of human
pharmaceutical products.
************************************************.
"End User Kits" means
****************************************.
"Excluded Assets" has the meaning set forth in Section
2.1(b).
"Excluded Contracts" means any oral or written contract,
commitment, purchase order, lease, note or other agreement to which
Seller is a party, other than the Assigned Contracts.
"Excluded Records" means (i) records related to human resources
and any other employee-related files and records; (ii) notes and
lab notebooks; (iii) personal files and records; and (iv) records
relating to the filing, prosecution, issuance, maintenance,
enforcement or defense of any intellectual property rights not
included in the Designated Intellectual Property or related to the
Abarelix License.
"European Marketing Region" means
*******************************.
"Final Allocation" has the meaning set forth in Section
2.2(b).
"FDA" means the United States Food and Drug Administration, or
any successor agency with substantially the same responsibility for
regulating the development, manufacture and sale of human
pharmaceutical products.
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
4
"GAAP" means generally accepted accounting
principles as used in the United States of America, consistently
applied.
"German Marketing Authorization" means the Certificate of
Registration with respect to Plenaxis â Product received by PRAECIS Europe from BfArM on September 27,
2005 to market Plenaxis â Product in Germany, together with all amendments, supplements
and updates thereto.
"Governmental Authority" means any governmental department,
commission, board, bureau, agency, court or other instrumentality
of any country, or any state, county, jurisdiction, municipality or
other political subdivision of such country.
"Governmental Consents" has the meaning set forth in Section
3.3(a).
"Governmental Filings" registrations, filings and notices with
or to Governmental Authorities.
"Gross Sales" means *********************.
"Incremental Consideration" has the meaning set forth in Section
2.4(a)(i).
"INDs" means the investigational new drug applications listed on
Schedule 1.1(e) .
"Indemnified Party" has the meaning set forth in Section
5.3(a).
"Indemnifying Party" has the meaning set forth in Section
5.3(a).
"Indiana University Intellectual Property" means the patents and
other intellectual property covering GnRH antagonist compounds,
including abarelix (PPI-149), the active ingredient of Plenaxis
â Product, licensed to Seller under
the Abarelix License.
"Information" has the meaning set forth in Section 6.1(a).
"Initial Regulatory Target Countries" means
*******************.
"Intangible Property Rights" has the meaning set forth in
Section 2.1(a)(iv).
"Knowledge of Seller" or "Seller’s Knowledge" has the
meaning set forth in Article III.
"Knowledge of Buyer" has the meaning set forth in Article
IV.
"Law" means any federal, state, local or foreign law, statute or
ordinance, or any
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
5
rule, regulation or regulatory requirement
promulgated by any Governmental Authority.
"Lien" means any lien, charge, claim, pledge, security interest,
conditional sale agreement or other title retention agreement,
lease, mortgage, security agreement, right of first refusal,
option, restriction, license, covenant, or other encumbrance, other
than (i) mechanic’s, materialmen’s, and similar liens
and (ii) liens on goods in transit incurred pursuant to documentary
letters of credit, in each case arising in the Ordinary Course of
Business of Seller and not material to the Acquired Assets.
"MAA" means the marketing authorization application submitted by
PRAECIS Europe to BfArM on June 23, 2003 (as supplemented or
amended from time to time).
"Manufacturing Contracts" means Contracts relating to the
manufacture of Plenaxis â
Product which are in effect on the Closing
Date, all of which Manufacturing Contracts are set forth on
Schedule 1.1(c) .
"Marketing Region" means **************************.
"Material Third Party Consents" means Third Party Consents, if
any, required under any Manufacturing Contract.
"Medical Product Regulatory Authority" means any Governmental
Authority that regulates the safety, efficacy, manufacture,
investigation, sale or marketing of pharmaceuticals, medical
products, biologics or biopharmaceuticals, including, without
limitation, the FDA and EMEA.
"Medicare National Coverage Determination" means Seller’s
files relating to the determination by the Centers for Medicare and
Medicaid Services with respect to Plenaxis â Product, listed as NCD Section Number 110.19.
"Minimum Annual Commitment Payments" means the payment amounts
set forth opposite the name of each Manufacturing Contract or the
reference to the Baxter Agreement, in each case listed on
Schedule 1.1(d) .
"Mutual Recognition Procedure" means the procedure whereby a
Regulatory Target Country may recognize the German Marketing
Authorization in accordance with Article 28(4) of Directive
2001/83/EC. Such terms also include any analogous or
successor procedure under any successor legislation.
"NDA" means the New Drug Application (No. 21-320) approved by
the FDA, together with all amendments, supplements and updates
thereto.
"NDA Assumption Letter" has the meaning set forth in Section
2.1(e).
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
6
"NDC Number" means a National Drug Code number,
as listed with the FDA.
"Net Sales" means *****************.
"Net Sales Deductions" means ****************.
"Order" means any order, judgment, decree or ruling of any
Governmental Authority or arbitrator.
"Ordinary Course of Business" means an action that is in
compliance with applicable Laws and is generally consistent in all
material respects with the past practices of Seller and its
Affiliates with respect to Seller’s Product Operations or
other activities in respect of the Acquired Assets in the twelve
(12) months preceding the effective date of this Agreement.
"Parties" has the meaning set forth in the first paragraph of
this Agreement.
"Permitted Liens" means Liens for Taxes that are not yet due and
payable andLiens arising from any actions of Buyer.
"Person" means an individual, a corporation, a limited liability
company, a partnership, an association, a trust or other entity or
organization, including a federal, state, local or foreign
government or regulatory entity or political subdivision or an
agency or instrumentality thereof.
"Plenaxis â
Product" means
*******************.
"PRAECIS Europe" means PRAECIS Europe Limited, a private limited
company incorporated in England and Wales.
"Preliminary Allocation" has the meaning set forth in Section
2.2(b).
"Proceeding" shall mean any action, suit, litigation,
arbitration, proceeding (including any civil, criminal,
administrative, investigative or appellate proceeding),
prosecution, contest, hearing, inquiry, inquest, audit, examination
or investigation brought or conducted by or before any Governmental
Authority or any arbitrator or arbitration panel.
"Product Operations" means the development (preclinical and
clinical), manufacture (including the right to have manufactured),
marketing, distribution and sale of Plenaxis â Product.
"Product Records" means collectively (i) regulatory and other
reports (including
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
7
pharmacovigilance reports), information on
adverse events, written contact regulatory reports and formal
minutes with any Governmental Authority, any documents (including,
without limitation, clinical and pre-clinical animal study data)
relating to the Registrations or to the subject matter of the
Registrations, in each case to the extent relating exclusively to
the Plenaxis â
Product or
Seller’s Product Operations and for the period commencing no
earlier than 1995, and (ii) records for the period commencing no
earlier than 1995 relating to the filing, prosecution, issuance,
maintenance, enforcement or defense of the Designated Intellectual
Property or in relation to the Abarelix License, in the case of (i)
and (ii) that are owned or controlled by or otherwise in the
possession of Seller as of the Closing Date and except to the
extent included in or primarily related to any Excluded Assets or
Retained Liabilities and excluding the Excluded Records.
"Purchase Price" has the meaning set forth in Section
2.2(a).
"Quarter" has the meaning set forth in Section 2.4(c).
"Registration Assumption Letters" has the meaning set forth in
Section 2.1(e).
"Registrations" means the NDA, the German Marketing
Authorization and the investigational new drug applications listed
in Schedule 1.1(e) .
"Registration Transfer Letter" has the meaning set forth in
Section 2.1(e).
"Regulatory Approval" means recognition by a Regulatory Target
Country of the German Marketing Authorization in accordance with
the Mutual Recognition Procedure and any approval to market
Plenaxis â Product in any other country or
territory.
"Regulatory Target Countries" means **********************.
"Rel-Ease™" means Seller’s proprietary depot drug
delivery technology as described under the Seller’s
Rel-Ease™ Patents as of the date of this Agreement.
"Rel-Ease™ License" means the License Agreement,
substantially in the form of Exhibit A ,
**********************.
"Retained Liabilities" has the meaning set forth in Section
2.1(d).
"Royalties" has the meaning set forth in Section 2.4(a)(ii).
"Royalty Bearing IP" means *****************.
"Royalty Term" has the meaning set forth in Section 2.4(b).
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
8
"Sale" (as a noun) means
***************************.
"Sales Statement" has the meaning set forth in Section
2.4(c).
"Section 1060 Forms" has the meaning set forth in Section
2.2(b).
"Seller" has the meaning set forth in the first paragraph of
this Agreement.
"Seller Indemnitees" has the meaning set forth in Section
5.2.
"Seller Licensed Party Consideration" means
******************.
"Seller’s NDC Number" means the NDC Number that has been
used by Seller in connection with Plenaxis â Product prior to
Closing.
"Seller’s Product Operations" means any Product Operations
conducted by Seller through the Closing Date.
"Seller Purposes" has the meaning set forth in Section
6.1(b).
"Seller’s Rel-Ease™ Patents" means the
Seller’s issued patents listed on Schedule 1.1(f)
.
"Shares" means all of the issued and outstanding shares of
PRAECIS Europe as identified on Schedule 1.1(g) .
"Taxes" (and with correlative meanings, "Tax" and "Taxable")
means all taxes of any kind imposed by a Governmental Authority,
including but not limited to those on, or measured by or referred
to as income, gross receipts, financial operation, sales, use, ad
valorem, value added, alternative or add-on minimum, franchise,
profits, license, withholding, payroll (including all contributions
or premiums pursuant to governmental social security laws or
pursuant to other tax laws and regulations), employment, excise or
severance and any interest, fines, penalties, assessments or
additions to tax imposed with respect to such items or any contest
or dispute thereof.
"Tax Returns" means all reports, returns, schedules and any
other documents required to be filed with a Governmental Authority
(including federal, state, local and foreign) with respect to
Taxes, including any attachments, schedule and amendment
thereof.
"Third Party" means any entity other than Seller or Buyer and
their respective Affiliates.
"Third Party Claim" has the meaning set forth in Section
5.3(a).
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
9
"Third Party Consents" has the meaning set forth
in Section 3.3(b).
"Trademark Rights" has the meaning set forth in Section
2.1(a).
"UK Business Day" means any day other than (i) a Saturday or a
Sunday or (ii) a day on which banking institutions located in
the United Kingdom are permitted or required by law to remain
closed.
"Valid Claim" means a claim of an issued and unexpired patent
that has not been held permanently revoked, unenforceable or
invalid by a decision of a court or other Governmental Authority of
competent jurisdiction, unappealable or un-appealed within the time
allowed for appeal, and that has not been admitted to be invalid or
unenforceable through reissue or disclaimer or otherwise.
ARTICLE II
ASSET PURCHASE
(a)
Transfer of Assets . Upon and subject to the terms and
conditions set forth in this Agreement, at the Closing, Seller
shall sell, convey, assign, transfer and deliver to Buyer, and
Buyer shall purchase and acquire from Seller, all of Seller’s
right, title and interest in and to the following assets,
properties and rights of Seller (the " Acquired Assets "),
excluding, however, the Excluded Assets:
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(i)
all of Seller’s rights under the Assigned Contracts, with
respect to the period following Closing;
(ii)
the Registrations, subject, however, to Section 6.1(b);
(iii) the
name "Plenaxis" and any variant thereof, the trademarks and trade
names and all registrations thereof and all related registration
applications set forth on Schedule 1.1(b) and all proceeds
of the foregoing and the right to sue for past, present and future
infringements of any of the foregoing and all future proceeds of
such suits (the " Trademark Rights "), and the domain names
set forth on Schedule 1.1(b) ;
(iv) the
Designated Intellectual Property (other than the Trademark Rights),
and other intangible property rights owned by Seller as of the
Closing Date to the extent primarily related to Plenaxis
â Product or
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
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Seller’s Product Operations, including, to
the extent so related, trade secrets, technical information and
know-how (collectively, the " Intangible Property Rights "),
it being understood for the avoidance of doubt that Intangible
Property Rights does not include Seller’s rights under the
Abarelix License or Seller’s rights with respect to
Rel-Ease™ or Seller’s Rel-Ease™
Patents;
(v)
all brochures and other promotional and printed materials, trade
show materials (including displays), videos, web pages, advertising
and/or marketing materials, package inserts and packaging materials
(all in physical form, pdf, quark, or other electronic file and
camera-ready artwork) in Seller’s possession or under its
control as of the Closing Date previously used exclusively in
connection with Seller’s promotion and sale of the Plenaxis
â Product; provided , however , that Seller
shall be obligated to provide only one copy of any electronic file
containing any of the foregoing;
(vi)
copies of all customer and supplier lists, marketing studies and
consultant reports related exclusively to the Plenaxis â Product or
Seller’s Product Operations to the extent maintained by
Seller and as in existence and in Seller’s possession or
under its control as of the Closing Date, and all complaint files
and adverse event files related exclusively to the Plenaxis
â Product or Seller’s Product Operations and as in
existence and in Seller’s possession or under its control as
of the Closing Date;
(vii) all
Closing Product Materials;
(viii) all the
goodwill of Seller’s Product Operations;
(ix)
all of Seller’s right, title, and interest in and to the
Plenaxis â Product as of the Closing Date, including all rights of
Seller and its Affiliates to develop, manufacture, make and have
made, offer to sell, sell, distribute, promote, and use the
Plenaxis â
Product, to the extent Seller has such
rights;
(x)
the Rel-Ease™ License;
(xi)
the manufacturing equipment located at Baxter Pharmaceutical
Solutions LLC and which is used or held for use in the operation
and conduct of Seller’s Product Operations;
(xii) all
Product Records, to the extent not covered by any of the
foregoing;
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
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(xiii) the
Medicare National Coverage Determination;
(xiv) the Shares;
and
(xv) all other
assets, properties and rights owned by Seller as of the Closing
Date principally used in Seller’s Product Operations or
otherwise principally used in relation to Plenaxis â
Product.
Such Acquired Assets shall be free and clear of all Liens, other
than Permitted Liens. Notwithstanding anything contained
herein, Seller may retain two (2) archival copies of (A) the
Registrations, (B) the Medicare National Coverage Determination,
(C) any Product Records, and any supplements and associated
materials related to the foregoing items (A) and (B), in each case
solely for legal, regulatory, Tax or accounting purposes.
This Agreement shall not constitute an agreement to assign any
Acquired Asset (including any Assigned Contract), or any claim or
right arising thereunder if an attempted assignment thereof,
without consent of a Third Party, would constitute a breach or
other contravention of any agreement with respect to such Acquired
Asset. Seller and Buyer will each use reasonable commercial
efforts (but without any payment of money by Seller, other than
out-of-pocket legal expenses) to obtain the consent of the other
party or parties to any such Acquired Asset (including any Assigned
Contract) or any claim or right arising thereunder for the
assignment thereof to Buyer. If such consent is not obtained,
or if an attempted assignment of any such Acquired Asset (including
any Assigned Contract) or claim or right would be ineffective or
would adversely affect the rights of Buyer thereunder so that Buyer
would not in fact receive all such rights, Buyer shall not, except
as provided in this sentence, assume liabilities or obligations
with respect thereto, and Seller shall at its expense effect an
alternate arrangement, in the form of a sublicense, sublease,
subcontract, operating agreement or other arrangement, in any case
reasonably satisfactory to Buyer, which results in Buyer obtaining
all the benefits and assuming the liabilities and other obligations
with respect to any such Acquired Asset or Seller shall enforce for
the benefit of Buyer with Buyer assuming Seller’s
obligations, any and all rights of Seller against a Third
Party. Seller will promptly pay to Buyer when received all
monies received by such Party under or with respect to any such
Acquired Asset (including any Assigned Contract) as to which such
arrangement has been entered into, or any claim or right or any
benefit arising thereunder, except to the extent the same
represents an Excluded Asset as contemplated by Section 2.1(b)
below. For the avoidance of doubt, nothing under this Section
2.1(a) or under Section 2.6 shall require Seller to effect the
recordation of any assignments of any Trademark Rights.
(b)
Excluded Assets . Notwithstanding anything to the contrary
in this Agreement, Seller is not selling, conveying, assigning,
transferring or delivering to Buyer any assets, properties or
rights of Seller other than those specifically identified in
Section 2.1(a). The term "Excluded Assets" shall mean:
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
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(i)
any right, title or interest, including without limitation, any
rights in any issued United States and foreign patents or other
intellectual property and pending United States and foreign patents
or other intellectual property applications, relating to
Seller’s Rel-Ease™ drug delivery technology and depot
formulation, but excluding rights granted to Buyer pursuant to the
Rel-Ease™ License;
(ii)
any Accounts Receivable (including Accounts Receivable with respect
to Plenaxis â Product which has been shipped prior to the Closing),
and, for the avoidance of doubt, any cash, cash equivalents, bank
deposits or similar cash items, or prepaid expenses (other than
royalties) of Seller and its Affiliates, in each case as of the
Closing (whether or not reflected on the books of Seller or its
Affiliates as of the Closing Date);
(iii) any
rights, claims and credits, including all guaranties, warranties,
indemnities and similar rights in favor of Seller or any of its
Affiliates or any of their respective employees to the extent
relating to (A) any other Excluded Asset, (B) any Excluded
Liability or (C) any matter to the extent Seller indemnifies any
Buyer Indemnitees pursuant to Article V;
(iv) any
Excluded Records; and
(v)
any other assets, properties and rights set forth on Schedule
2.1(b)(v) .
(c)
Assumed Liabilities . Buyer shall, and hereby does, assume
and agree to pay, perform and discharge when due the following
liabilities and obligations (the " Assumed Liabilities
"):
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(i)
all liabilities arising, and all obligations of Seller to be
performed, from and after the Closing under the Assigned Contracts;
provided , however , that any obligations in respect
of Minimum Annual Commitment Payments shall be included in Assumed
Liabilities whether or not such payments are required to be paid
prior to the Closing;
(ii)
all liabilities and obligations of Seller and/or PRAECIS Europe
under the Registrations to the extent to be performed from and
after the Closing , including with respect to the
post-marketing commitments and pharmacovigilance obligations
relating to FDA approval of the NDA and any outstanding commitments
under the German Marketing Authorization;
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
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(iii) all
liabilities with respect to all actions, suits, proceedings,
disputes, claims or investigations arising out of or related to the
ownership, use, maintenance or operation of any Abarelix Product,
the Acquired Assets or the Product Operations after the Closing,
subject to the proviso to clause (i) above;
(iv) all
liabilities and obligations relating to the replacement, return or
refund of the purchase price of any Abarelix Product distributed or
sold by or on behalf of Buyer, any of its Affiliates or any Buyer
Licensed Party after the Closing;
(v)
all liabilities and obligations relating to any claim for breach of
warranty in respect of (i) any Abarelix Product manufactured,
distributed or sold by or on behalf of Buyer, any of its Affiliates
or any Buyer Licensed Party after the Closing or (ii) the Closing
Product Materials;
(vi) all
liabilities and obligations arising out of or relating to any
product liability claim involving (i) any Abarelix Product
manufactured, distributed or sold by or on behalf of Buyer, any of
its Affiliates or any Buyer Licensed Party after the Closing or
(ii) the Closing Product Materials, in each case including, without
limitation, injury to or death of persons or damage to or
destruction of property, to the extent such injury, death, damage
or destruction occurs after the Closing; and
(vii) all other
liabilities and obligations not specifically referred to in
subsections (i) through (vi) above (subject to the proviso to
clause (i) above), arising out of or related to the ownership, use,
maintenance or operation of any Abarelix Product, the Acquired
Assets or the Product Operations after the Closing, including,
without limitation, the tax liabilities to which reference is made
in the second sentence of Section 7.15(b).
(d)
Retained Liabilities . Buyer shall not be obligated
hereunder to be responsible for, assume or agree to pay, perform or
discharge, and Seller shall remain responsible and liable for, any
and all liabilities and obligations of Seller (whether known or
unknown, whether absolute or contingent, whether liquidated or
unliquidated and whether due or to become due), other than the
Assumed Liabilities (the " Retained Liabilities ").
(e)
Registrations . On the Closing Date, Seller shall assign or
transfer to Buyer, and Buyer will assume, the Registrations to the
extent provided in this Agreement. Without limiting the
generality of the foregoing, attached as Exhibits B-1
through B-4 are copies of the letters to be duly executed by
and submitted by or on behalf of Seller to the
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
14
FDA on the Closing Date authorizing the transfer
of ownership of the NDA and the INDs from Seller to Buyer (each
such letter, a " Registration Transfer Letter ") pursuant to
21 C.F.R. § 314.72. As soon as practicable after the
Closing and the receipt by Buyer of copies of the Registration
Transfer Letters and evidence of the FDA’s receipt of each
such letter, Buyer shall execute and submit to the FDA the letters,
substantially in the form of the letters attached as Exhibits
C-1 through C-4 , acknowledging Buyer’s commitment
to assume ownership of the NDA and the INDs (collectively, the "
Registration Assumption Letters ").
(a)
Purchase Price . In consideration of the sale and transfer
of the Acquired Assets, Buyer shall (i) reimburse Seller for any
Minimum Annual Commitment Payments made by Seller and documented
for Buyer, in accordance with Section 2.5 and (ii) pay the
Incremental Consideration, the Seller Licensed Party Consideration
and the Royalties, each as provided in Section 2.4 (the payments
contemplated by subsections (i) and (ii), collectively, the "
Purchase Price ") and (iii) assume the Assumed Liabilities
as provided in Section 2.1(c). All payments under this
Agreement to Seller shall be made in United States Dollars by wire
transfer of immediately available funds to an account designated by
Seller in writing at least two (2) Business Days prior to the date
that the payment is due and shall be non-refundable.
(b)
Allocation .
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(i)
Buyer shall propose to Seller an allocation of the Purchase Price
********************** plus the Assumed Liabilities among the
Acquired Assets for tax purposes (the " Consideration ") in
accordance with the methodology required by Section 1060 of the
Code within forty-five (45) Business Days after the Closing Date
(the " Preliminary Allocation "). Within ten (10)
Business Days following the receipt of the Preliminary Allocation,
Seller shall have the right to provide Buyer with a written notice
objecting to the Preliminary Allocation. Within five (5)
Business Days following receipt of Seller’s objections, if
any, to the Preliminary Allocation (the " Allocation Resolution
Period "), Buyer and Seller shall negotiate in good faith to
resolve any differences regarding the Preliminary Allocation, and
Buyer shall make such changes as are reasonably requested by Seller
(as so resolved, the " Final Allocation "). If Seller does
not object to the Preliminary Allocation within ten (10) Business
Days a set forth above, the Preliminary Allocation shall be deemed
to be the Final Allocation for purposes of this Agreement.
(ii)
If Buyer and Seller are unable to resolve any differences with
regard to the Preliminary Allocation within the Allocation
Resolution Period, then Buyer and Seller shall jointly engage
an
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
15
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internationally recognized accounting firm (the "
Accountant "). The Accountant shall resolve any such
differences based upon its appraisal of the fair value of the
Acquired Assets among which the Consideration is to be
allocated. Buyer and Seller shall promptly provide to the
Accountant such information as the Accountant may reasonably
request in connection with the preparation of such allocation and
shall request that the Accountant prepare and deliver to Buyer and
Seller such allocation as promptly as practicable. Buyer and
Seller shall each pay 50% of the fees and expenses of the
Accountant for its services under this Section 2.2(b)(ii).
The resolution by the Accountant of the matters set forth in this
Section 2.2(b)(ii) shall be conclusive and binding upon Buyer and
Seller. Buyer and Seller agree that the procedure set forth
in this Section 2.2(b)(ii) for resolving disputes with respect to
the Preliminary Allocation shall be the sole and exclusive method
for resolving any such disputes; provided , however ,
that this provision shall not prohibit either Party from
instituting litigation to enforce any ruling of the
Accountant. The Accountant’s determination shall be
deemed to be the Final Allocation for purposes of this
Agreement.
(iii)
Buyer and Seller shall (x) be bound by the Final Allocation for all
Taxes purposes, (y) timely file IRS Form 8594 and all Tax Returns
required to be filed in connection with the Final Allocation (and
any other forms or reports required to be filed pursuant to Section
1060 of the Code or any comparable provisions of U.S. local or
state, or foreign law (the " Section 1060 Forms ")), in
accordance with the Final Allocation, and (z) take no position
inconsistent with the Final Allocation in any Section 1060 Form or
Tax Return, any audit or examination by, or any proceeding before,
any Governmental Authority or otherwise, unless otherwise required
by the final determination of a Governmental Authority. Buyer
and Seller shall make proper adjustments to the Final Allocation at
the time Buyer makes any of the payments contemplated by this
Section 2.2(a)(iii).
(iv) In
the event that the Final Allocation is disputed by any Governmental
Authority, the Party receiving notice of such dispute shall
promptly notify and consult with the other Party and keep such
other Party apprised of material developments concerning resolution
of such dispute. The Party receiving notice of such dispute
shall control any examination, investigation, audit or other
proceeding resulting from such dispute by any taxing authority
regarding the Final Allocation; provided , however ,
that the other Party shall have the nonexclusive right to
participate in such examination, investigation, audit or other
proceeding at its sole cost and expense.
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
16
(c)
Payments of the Purchase Price . Any and all payments of the
Purchase Price as set forth in Section 2.2(a) shall be made free
and clear of and without deduction for any and all Taxes. If
Buyer shall be required by applicable Law to deduct any such Taxes
from or in respect of any such payment, then (i) such payment shall
be increased as may be necessary so that after making all required
deductions (including deductions applicable to additional sums
payable under this Section 2.2(c)) Seller shall receive an amount
equal to the payment it would have received had no such deductions
been made, (ii) Buyer shall make such deductions and (iii) Buyer
shall pay the full amount deducted to the relevant taxation
authority or other authority in accordance with applicable
Law.
(a)
Time and Location . The closing of the transactions
contemplated by this Agreement (the " Closing ") shall take
place, and is taking place, at the offices of Skadden, Arps, Slate,
Meagher & Flom LLP in Boston, Massachusetts (or at such other
place as the parties may designate in writing), commencing at 10:00
a.m., Boston time, on the date of this Agreement.
(b)
Actions at the Closing . At the Closing:
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(i)
Seller shall execute and deliver to Buyer a Bill of Sale
substantially in the form of Exhibit D ;
(ii)
Seller shall execute and deliver the Assignment of Intellectual
Property substantially in the form of Exhibit E , suitable
for recordation in the United States Patent and Trademark Office
and/or United States Copyright Office, as applicable, or any other
applicable Governmental Authority to evidence the assignment of
intellectual property rights thereunder;
(iii)
Seller shall deliver to Buyer a copy of each executed Registration
Transfer Letter;
(iv)
Seller and Buyer shall execute and deliver to each other
counterparts of the Rel-Ease™ License;
(v)
Seller and Buyer shall execute and deliver to each other
counterparts of an Assignment and Assumption Agreement
substantially in the form of Exhibit F ;
(vi)
Seller shall deliver (or cause to be delivered) to Buyer all of the
Governmental Consents set forth in Schedule 3.3(a) (not
otherwise identified on such Schedule as not being delivered);
CONFIDENTIAL INFORMATION OMITTED AND FILED
SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
17
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(vii) Seller
shall deliver (or cause to be delivered) to Buyer a copy of duly
executed Material Third Party Consents and other Third Party
Consents to the extent obtained by Seller through the Closing
Date;
(viii) Seller shall
deliver to Buyer a certificate of corporate good standing of Seller
in Delaware and a certificate as to the incumbency of officers of
Seller executing this Agreement and the Ancillary Agreements and
the adoption by Seller’s board of directors of authorizing
resolutions with respect to the transactions contemplated by this
Agreement;
(ix)
Buyer shall deliver to Seller a certificate of good standing (or
analogous equivalent) of Buyer in England and Wales and a
certificate as to the incumbency of officers of Buyer executing
this Agreement and the Ancillary Agreements and the adoption by
Buyer’s board of directors of authorizing resolutions with
respect to the transactions contemplated by this Agreement; and
(x)
Seller shall deliver to Buyer certificate(s) representing the
Shares, duly endorsed (or accompanied by duly executed stock
powers), for transfer to Buyer.
The agreements and instruments referred to in clauses (i), (ii),
(iii), (iv) and (v) above and the Registration Assumption Letters
are referred to herein as the "Ancillary Agreements."
(a)
Additional Consideration .
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(i)
Incremental Consideration . Buyer shall pay to Seller
*****************************. The payments described in this
Section 2.4(a)(i) are collectively referred to as the "Incremental
Consideration". At such time as Buyer delivers the Sales
Statement to Seller, Buyer shall pay to Seller the Incremental
Consideration due hereunder for the applicable Quarter.
********************.
(ii)
Seller Licensed Party Consideration . Buyer shall
notify Seller within three (3) Business Days of the receipt by
Buyer or any of its Affiliates of any Buyer Licensed Party
Consideration. Buyer shall pay or cause to be paid to Seller
the Seller Licensed Party Consideration within ten (10) Business
Days of the receipt by Buyer or any such Affiliate of such Buyer
Licensed Party Consideration, together with a calculation of such
Seller Licensed Party Consideration, including a breakdown of
any
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ASTERISKS (*) DENOTE SUCH OMISSIONS.
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(b)
Conduct of the Product Operations .
Buyer shall, and shall cause its controlled Affiliates to, use
Commercially Reasonable Efforts to commercialize, or cause to be
commercialized, Plenaxis â Product in
**********. Buyer shall use Commercially Reasonable Efforts
to obtain Regulatory Approval for Plenaxis â Product in
each of the Regulatory Target Countries , including, in the
Initial Regulatory Target Countries only, using Commercially
Reasonable Efforts to commence, as soon as practicable and no later
than one hundred eighty (180) days after the Closing Date, the
Mutual Recognition Procedure for Plenaxis â Product. After obtaining a Regulatory Approval in
any Regulatory Target Country, Buyer shall, and shall cause its
controlled Affiliates to, use Commercially Reasonable Efforts to
commercialize, or cause to be commercialized, Plenaxis
â Product in the Regulatory Target
Countries. Buyer shall notify Seller within two (2) Business
Days after commencing the Mutual Recognition Procedure for
Plenaxis â
Product in a Regulatory Target Country or
filing for the applicable Regulatory Approval in any other
country. For purposes of this Section 2.4(b), "commencing"
the Mutual Recognition Procedure for Plenaxis â Product in a
Regulatory Target Country means Buyer’s confirmation both to
the applicable Governmental Authority in ******** and in such
Regulatory Target Country of the date of dispatch of the Dossier to
such Regulatory Target Country. For the avoidance of doubt,
none of the following shall, in and of itself, constitute a failure
to use Commercially Reasonable Efforts under this Section
2.4(b): (i) not commencing or causing to be commenced a
Mutual Recognition Procedure in any Regulatory Target Country other
than an Initial Regulatory Target Country; (ii) ceasing or causing
to be discontinued efforts to obtain Regulatory Approval in any
Regulatory Target Country; or (iii) not commencing or continuing,
or causing not to be commenced or continued, efforts to
commercialize Plenaxis â Product in any Regulatory
Target Country.
(c)
Reports . Buyer shall deliver to Seller, within
forty-five (45) days after the last day of each calendar quarter
(each, a " Quarter "), a statement (each, a " Sales
Statement "), setting forth (i) the aggregate amount of Gross
Sales by or on behalf of Buyer or its Affiliates for each Abarelix
Product (including unit quantities) for such Quarter, (ii) the
aggregate Net Sales for such Quarter, including a breakdown of the
Net Sales Deductions (which deductions shall be aggregated by
category), for each Abarelix Product in each Marketing Region
**********************, (iii) the aggregate Cost Adjusted Sales for
such Quarter, (iv) ********************* and (v) the calculation of
the Incremental Consideration for such Quarter and (vi) the
calculation of the Royalties for such Quarter.
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ASTERISKS (*) DENOTE SUCH OMISSIONS.
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(d)
Late Payments; Collections . Any amount not paid when due
under this Section 2.4 shall bear interest at an annual rate equal
to the lesser of (i) the highest U.S. Prime Interest Rate per annum
published in the Wall Street Journal on the first Business Day
after the payment first became due, plus three (3) percentage
points, and (ii) the highest rate permitted by applicable
law.
(e)
Books and Records; Audits . Notwithstanding
Section 6.1 to the contrary, Buyer and its Affiliates shall keep
full, true and accurate books of account sufficient to determine
the amounts payable pursuant to this Section 2.4.
Seller shall have the right to have the books and records of
Buyer and its Affiliates audited by a qualified independent
certified public accounting firm selected by Seller, subject to
Buyer’s approval, which approval shall not be unreasonably
withheld or delayed, under appropriate confidentiality provisions,
to ascertain the accuracy of the reports and payments under this
Section 2.4 for any year ending not more than thirty-six (36)
months prior to the date of such request. For the avoidance
of doubt, Seller’s audit right shall extend to ascertaining
the accuracy of Development Costs and reimbursed costs and expenses
which have been excluded in determining Buyer Licensed Party
Consideration. Such audit shall be conducted upon at least
ten (10) days’ advance written notice during normal business
hours, not more than once in each year, and in a manner that does
not interfere unreasonably with the business of the audited
entity. The accounting firm shall disclose to Seller only
whether such reports are correct or incorrect and the specific
details concerning any discrepancies. Subject to
Buyer’s right to dispute such amounts, any underpayment
determined by such audit shall promptly be paid by Buyer after
delivery to Buyer of such accounting firm’s report so
concluding. In the event such accounting firm concludes that
amounts were overpaid by Buyer during such period, subject to
Seller’s right to dispute such amounts, Seller shall promptly
repay Buyer the amount of such overpayment after delivery to Buyer
and Seller of such accounting firm’s written report so
concluding. Seller and Buyer shall treat all
financial information subject to review under this Section 2.4(e)
in accordance with the confidentiality provisions of this Agreement
and shall cause the accounting firm selected by it to enter into a
customary and mutually satisfactory confidentiality agreement with
Buyer obligating such firm to retain all such financial information
in confidence pursuant to such confidentiality agreement. If
Buyer has underpaid an amount due under this Section 2.4 by more
than ten percent (10%) of the Royalties due hereunder for the
period being reviewed, Buyer shall reimburse Seller for the
reasonable fees and costs charged by such accounting firm (with all
fees and costs of the audit to be borne by Seller in all other
cases).
Seller shall pay any Minimum Annual Commitment Payments
payable in respect of the year 2006 and forthwith provide evidence of such payments to Buyer
who shall reimburse Seller for the amount of such Minimum
Annual Commitment Payments thus paid, promptly upon receipt of
evidence of such payments but in any event no later than ten
(10) UK Business Days after the Closing Date.
For the avoidance of doubt, other than with
respect to Minimum Annual Commitment
CONFIDENTIAL INFORMATION
OMITTED AND FILED SEPARATELY
WITH THE SECURITIES AND EXCHANGE COMMISSION.
ASTERISKS (*) DENOTE SUCH OMISSIONS.
20
Payments payable in respect of the year 2006, this
Section 2.5 shall not limit Buyer’s obligations
under Section 2.1(c).
At any time and from time to time after the Closing Date, as and
when requested by any Party, the other Party shall promptly execute
and deliver, or cause to be executed and delivered, all such
documents, instruments and certi
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