SECOND AMENDMENT TO LICENSE AGREEMENT Relating to Encapsulated Cells Producing Viral Particles and Encapsulated Cells Expressing Biomolecules LICENSORS Bavarian Nordic A/S, reg. no. 16271187 a company incorporated in Denmark, whose registered office...
Exhibit 10.1
SECOND AMENDMENT TO LICENSE AGREEMENT
Relating to
Encapsulated Cells Producing Viral Particles
and
Encapsulated Cells Expressing Biomolecules
LICENSORS
Bavarian Nordic A/S, reg. no. 16271187
a company incorporated in Denmark, whose registered office is at Xxxxxxxxxxxx 00X,
XX-0000 Xxxxxxxxx, Xxxxxxxx
and
Helmholtz Zentrum Miinchen/GSF — Forschungszentrum
fur Umwelt u.
Gesundheit GmbH,
Ingolstadter Xxxxxxx. 0, X-00000 Xxxxxxxxxx, Xxxxxxxxxxx
and
LICENSEE
Bio Xxxx Xxxx XX,
Xxxxxxxx. 0, XX-0000 Xxxxx, Xxxxxxxxxxxxx
This Second Amendment to Licensee Agreement ("Second Amendment") is made effective as of the 1st day of October 2016 ("Effective Date of the Second Amendment") between:
| (1) | BAVARIAN NORDIC A/S, reg. no. 16271187, a company incorporated in Denmark, whose registered office is at Xxxxxxxxxxxx 00X, XX-0000 Xxxxxxxxx, Xxxxxxx ("BAVARIAN NORDIC") and | |
| (2) | Helmholtz Zentrum Munchen/GSF-Forschungszentrum fur Umwelt u. Gesundheit GmbH, Ingolstadter Xxxxxxx. 0, X-00000 Xxxxxxxxxx, Xxxxxxxxxxx ("GSF") (BAVARIAN NORDIC and GSF jointly referred to as "LICENSORS") and | |
| (3) | Bio Blue Bird AG, Pflugstr. 7, FL-9490 Vaduz, Liechtenstein ("LICENSEE"). |
| WHEREAS | LICENSEE and LICENSORS entered Into a License Agreement on 6 July 2005 ("License Agreement") whereby LICENSEE was granted a non-exclusive license to, in particular, further develop, make, have made (including services under contract for Licensee or sub-licensee, by Contract Manufacturing Organizations, Contract Research Organisations, Consultants, Logistics Companies or others), obtain marketing approval, sell and offer for sale the Licensed Product or otherwise use the Licensed Patent Rights in the Territory within the Field of this Agreement. |
| WHEREAS | LICENSEE and LICENSORS amended the License Agreement on 20 December 2006 ("Amendment") to reflect: (i) the license granted shall be exclusive; (ii) a royalty rate increase; (iii) LICENSEE taking over expenses; and (iv) to make clear that the license will survive as a license granted by one of the LICENSORS if the other LICENSOR rejects performance under the License Agreement due to any actions or declarations of insolvency. |
| WHEREAS | LICENSEE and LICENSORS now desire to further amend the License Agreement in order to include the right to import, reflect Ownership and Notification of Improvements, clarify which provisions survive expiration or termination of the License Agreement, to provide rights to the LICENSEE to the Clinical Data after the expiration of the Licensed Patent Rights and to change the Notice address and recipients of LICENSEE. |
It is agreed:
Clause 3.1 of the License Agreement shall be deleted and replaced with the following:
| 3.1 | License to LICENSEE. Subject to the terms of this Agreement, LICENSORS hereby grant to LICENSEE the exclusive irrevocable (except as provided for in clause 9.2) royalty-bearing, license, with the right to sublicense in accordance with Clause 3.2, under the Licensed Patent Rights to further develop, make, have made (including services under contract for Licensee or sub-licensee, by Contract Manufacturing Organizations, Contract Research Organizations, Consultants, Logistics Companies or others), obtain marketing approval, sell, import and offer for sale the Licensed Product or otherwise use the Licensed Patent Rights in the Territory within the Field of this Agreement. |
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Clause 4.1 of the License Agreement shall be deleted and replaced with the following:
| 4.1 | BAVARIAN NORDIC hereby grants LICENSEE and any sub-licensee, the exclusive right to use the Clinical Data (Annex 1) that may be deemed necessary or appropriate in order for LICENSEE or any sub-licensee to develop, make, have made (including services under contract for LICENSEE or sub-licensee, by Contract Manufacturing Organizations, Contract Research Organizations, Consultants, Logistics Companies or others), obtain marketing approval, sell, import and offer for sale the Licensed Products or otherwise use the Clinical Data pursuant to Clause 3. |
Clause 6.3 of the License Agreement shall be deleted and replaced with the following:
| 6.3 | Patent Prosecution. LICENSORS shall have the sole and exclusive right, except as otherwise provided below, to file, prosecute
and maintain any patents with claims covering inventions in the Licensed Patent Rights. LICENSORS shall use good faith, diligent
efforts to file, prosecute, and maintain such patents, including Supplementary Protection Certificates ("SPC") and Patent
Term Extensions ("PTE") and the like, and shall consider the best interest of both LICENSEE and LICENSORS in so doing;
provided, however, that LICENSOR shall defer to the LICENSEES request as to which patent(s), if any, should be the subject of an
application for and/or selection of such SPC, PTE or the like. However, any such request by Licensee to obtain any such Patent
Term Extension shall be procured by a mutually agreed external counsel. LICENSEE is solely responsible for providing all information
required to obtain any Patent Term Extension, and within the relevant period for such filing, to said external counsel including,
but not limited to, the identity of the product subject to regulatory review, the identity of the patent for which extension is
being sought and the identity of each claim, all information needed to enable the eligibility of a patent for extension, the description
of the activities undertaken by the applicant, or the LICENSEE as the case may be, during the applicable regulatory review period,
and any other information required to obtain said Patent Term Extension. LICENSORS shall provide the external counsel all necessary
assistance in terms of documentation and declarations that pertain to said patents needed to obtain Patent Term Extension. As of the first day of January 2007 LICENSEE will bear LICENSORS' external attorneys' costs and official fees necessary for filing, prosecuting and maintaining any patent claims covering inventions in the Licensed Patent Rights. LICENSORS' internal costs will be borne by themselves. At the end of each calendar quarter LICENSORS shall send LICENSEE a detailed specification of external costs and fees incurred in that quarter, if any. Upon receipt of such specification LICENSEE shall pay the external costs and fees within one month to the invoicing LICENSOR. Upon request from the LICENSEE, the invoicing LICENSOR shall provide invoices or other documents evidencing the external costs and fees. Notwithstanding the foregoing, the cost incurred by an external counsel retained to procure a Patent Term Extension shall be invoiced to, and paid for directly, by LICENSEE. |
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If LICENSORS decline to file or prosecute a patent or maintain a patent within the Licensed Patent Rights, LICENSORS shall timely, at least three months before any relevant deadline, notify LICENSEE and LICENSEE may thereafter file and prosecute at its expense a patent or application or maintain a patent claiming such invention. LICENSORS shall in such case provide to LICENSEE all necessary assistance, in particular assignment declarations and copies of all relevant patent office correspondence and copies of the relevant patent application and all patent documents. As a result of its maintenance of such patents or filing and or prosecution of such patent applications (or paying any fees according to this Clause), LICENSEE shall obtain all rights in these patents (including SPCs and PTEs and the like) and patent applications for that jurisdiction and cease to be obliged to further pay royalties here based on said patents (including SPCs, PTEs and the like) or patent applications prosecuted or maintained at its own expense. |
Clause 9.3.1 of the License Agreement shall be deleted and replaced with the following:
| 9.3.1 | In the event of termination or expiry of this Agreement, the following provisions (Clauses) of this Agreement shall survive in their entirety (2.2, 6.7, 8, 9.3, 13.1, 13.2, 13.3, 14.1, 14.4, 14.7). |
The following Clause 9.3.3 shall be added to the License Agreement as follows:
| 9.3.3 | Upon expiration, but not earlier termination, pursuant to Section 9.1, Licensee will have a non-exclusive, irrevocable, perpetual, fully-paid license, with the right to sublicense, to use the Clinical Data (Annex 1) as set forth in Clause 4.1. |
The Notices "To LICENSEE", including "With copies to" set forth in Clause 14.7 of the License Agreement, are hereby deleted and restated as follows:
| To LICENSEE: | Bio Bluebird AG |
| Xxxxxxxxxxxx 0 | |
| XX-0000 | |
| Xxxxx, Xxxxxxxxxxxxx | |
| Attn: Xx. Xxxxxxx X. Xxxxxxxx |
| With copies to: | PharmaCyte Biotech, Inc. |
| 23046 Xxxxxxx xx xx Xxxxxxx | |
| Xxxxx 000 | |
| Xxxxxx Xxxxx, Xxxxxxxxxx 00000 XXX | |
| Attn: Xx. Xxxxxxx X. Xxxxxxxx |
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| If to GSF: |
Helmholtz Zentrum Munchen Deutsches Forschungszentrum fur Gesundheit und Umwelt (GmbH) |
| (now HMGU) | Legal Affairs |
| Ingolstadter Xxxxxxxxxxx 0 | |
| 00000 Xxxxxxxxxx | |
| Attn: Head of Legal Affairs and Head of Innovation Management (2016744) |
Except as amended and set forth above, the License Agreement shall continue in full force and effect.
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