Notice2021-19618
Prospective Grant of an Exclusive Patent License: Development and Commercialization of Allogeneic T Cell and Gene Therapy Vector Chimeric Antigen Receptor (CAR) Therapies Targeting CD22 Alone or in Combination With CARs Targeting CD19 for the Treatment of B-Cell Malignancies
Primary source
Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.
Published
September 13, 2021
Issuing agencies
Health and Human Services DepartmentNational Institutes of Health
Abstract
The National Cancer Institute, an institute of the National Institutes of Health, Department of Health and Human Services, is contemplating the grant of an Exclusive Patent License to practice the inventions embodied in the Patents and Patent Applications listed in the Supplementary Information section of this Notice to Sana Biotechnology Inc. Life Sciences Inc., ("Sana"), located in Seattle, Washington.
Full Text
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<title>Federal Register, Volume 86 Issue 174 (Monday, September 13, 2021)</title>
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[Federal Register Volume 86, Number 174 (Monday, September 13, 2021)]
[Notices]
[Pages 50895-50897]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2021-19618]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Prospective Grant of an Exclusive Patent License: Development and
Commercialization of Allogeneic T Cell and Gene Therapy Vector Chimeric
Antigen Receptor (CAR) Therapies Targeting CD22 Alone or in Combination
With CARs Targeting CD19 for the Treatment of B-Cell Malignancies
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
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SUMMARY: The National Cancer Institute, an institute of the National
Institutes of Health, Department of Health and Human Services, is
contemplating the grant of an Exclusive Patent License to practice the
inventions embodied in the Patents and Patent Applications listed in
the Supplementary Information section of this Notice to Sana
Biotechnology Inc. Life Sciences Inc., (``Sana''), located in Seattle,
Washington.
DATES: Only written comments and/or complete applications for a license
which are received by the National Cancer Institute's Technology
Transfer Center on or before September 28, 2021 will be considered.
[[Page 50896]]
ADDRESSES: Requests for copies of the patent applications, inquiries,
and comments relating to the contemplated Exclusive Patent License
should be directed to: Jim Knabb, Senior Technology Transfer Manager,
at Telephone: (240)-276-7856; or at Email: <a href="/cdn-cgi/l/email-protection#177d7e7a397c7976757557797e7f39707861"><span class="__cf_email__" data-cfemail="375d5e5a195c5956555577595e5f19505841">[email protected]</span></a>.
SUPPLEMENTARY INFORMATION:
Intellectual Property
E-080-2012-0: Human Monoclonal Antibodies Specific for CD22
1. US Provisional Patent Application 61/042,329, filed April 4,
2008 (E-080-2008-0-US-01);
2. International Patent Application PCT/US2009/039,080, Filed April
1, 2009 (E-080-2008/0-PCT-02);
3. US Patent Application: 12/934,214, filed September 23, 2010 (E-
080-2008-0-US-03);
4. US Patent Application 13/959,061, filed August 5, 2015 (E-080-
2008-0-US-04);
5. US Patent Application 15/012,023, filed February 1, 2016 (E-080-
2008-0-US-05);
6. US Patent Application 15/424,238, filed February 3, 2017 (E-080-
2008-0-US-06).
E-291-2012-0: M971 Chimeric Antigen Receptors
1. US Provisional Patent Application 61/717,960, filed October 24,
2012 (E-291-2012-0-US-01);
2. International Patent Application PCT/US2013/060332, filed
September 18, 2013 (E-291-2012-0-PCT-02);
3. Australia Patent Application No: 2019235926, filed September 2,
2020 (E-291-2012-0-AU-03);
4. Brazil Patent Application BR112015009003-6, filed April 22, 2015
(E-291-2012-0-BR-04);
5. Canada Application No: 2889055, filed September 18, 2013 (E-291-
2012-0-CA-05);
6. China Application No: 201380061387.5, filed May 25, 2015 (E-291-
2012-0-CN-06);
7. European Patent Application No: 13773468.7, filed September 18,
2013 (E-291-2012-0-EP-07);
8. India Patent Application No: 2344/CHENP/2015, filed September
18, 2013 (E-291-2012-0-IN-08);
9. Japan Application No: 539602/2015, filed April 24, 2015 (E-291-
2012-0-JP-09);
10. Russia Patent Application: 2015117237, filed May 7, 2015 (E-
291-2012-0-RU-10);
11. US Patent Application: 14/437,889, filed April 23, 2015 (E-291-
2012-0-US-11);
12. Hong Kong Patent Application: 16101891.0, filed February 19,
2016 (E-291-2012-0-HK-12);
13. Russia Patent Application: 2018116582, filed May 4, 2018 (E-
291-2012-0-RU-13);
14. Japan Patent Application: 2018-088908, filed May 2, 2018, (E-
291-2012-0-JP-14);
15. Australia Patent Application: 2018204257, filed June 14, 2018
(E-291-2012-0-AU-16);
16. US Patent Application: 16/107,271, filed August 21, 2018 (E-
291-2012-0-US-17);
17. Germany Patent Application: 13773468.7, filed April 22, 2015
(E-291-2012-0-DE-18);
18. Spain Patent Application: 13773468.7, filed April 22, 2015 (E-
291-2012-0-ES-19);
19. France Patent Application: 13773468.7, filed April 22, 2015 (E-
291-2012-0-FR-20);
20. Great Britain Patent Application: 13773468.7, filed April 22,
2015 (E-291-2012-0-GB-21);
21. Italy Patent Application: 13773468.7, filed April 22, 2015 (E-
291-2012-0-IT-22);
22. China Patent Application: 201910500128.7, filed June 11, 2019
(E-291-2012-0-CN-23);
23. US Patent Application: 16/869,792, filed May 8, 2020 (E-291-
2012-0-US-24).
E-106-2015-0: Chimeric Antigen Receptors Targeting Both CD19 and CD22
1. US Provisional Patent Application No.: 62/135,442, filed March
19, 2015 (E-106-2015-0-US-01);
2. International Patent Application PCTUS2016/023055, Filed March
18, 2016 (E-106-2015-0-PCT-02);
3. US Patent Application: 15/559,485. Filed September 19, 2017 (E-
106-2015-0-US-03).
E-017-2017-0: CD19/CD22 Bicistronic CAR Targeting Human B-Cell
Malignancies
1. US Provisional Patent Application No.: 62/135,442, filed May 15,
2017 (E-017-2017-0-US-01);
2. International Patent Application PCT/US2018/032,809, filed May
15, 2018 (E-017-2017-0-PCT-02);
3. Australia Patent Application No.: 2018269194, filed October 28,
2019 (E-017-2017-0-AU-03;
4. Canada Patent Application No: 3062433, filed May 15, 2018 (E-
017-2017-0-CA-04);
5. China Patent Application No.: 201880032676.5, filed Date: May
15, 2018 (E-017-2017-0-CN-05);
6. European Patent Application No.: 18733012.1, filed May 15, 2018
(E-017-2017-0-EP-06);
7. Japan Patent Application No.: 2019-563082, filed November 13,
2019 (E-017-2017-0-JP-07);
8. Korea Patent Application No.: 2019-7017289, filed December 13,
2019, (E-017-2017-0-KR-08);
9. Singapore Patent Application No.: 11201910499V, filed November
11, 2019 (E-017-2017-0-SG-09);
10. United States Patent Application No.: 16/613,187, filed
November 13, 2019 (E-017-2017-0-US-10).
The patent rights in these inventions have been assigned and/or
exclusively licensed to the government of the United States of America.
The prospective exclusive license territory may be worldwide, and
the fields of use may be limited to the following:
``Field 1: ``Ex vivo allogeneic CAR-T''
The development, manufacture and commercialization of chimeric
antigen receptor T cells (CAR-T cells) for the treatment of B cell
malignancies, wherein the CAR-T cells are engineered to express a
CAR that comprises the m971 binder and is mono-specific for CD22, or
is specific to both CD22 and CD19 (but are not engineered to bind to
any other B cell antigen), and the engineered CAR-T cells are
generated ex vivo using allogeneic T cells that are engineered to
over-express CD47.
Field 2: ``In vivo gene therapy vector''
The development, manufacture and commercialization of gene
therapy vectors encoding a chimeric antigen receptor construct (CAR
construct), wherein the CAR construct comprises either (i) a CD22
binder m971 or (ii) the CD22 binder m971 and a CD19 binder, but, in
each case (i) and (ii), comprises no other binder against a B cell
antigen. For the avoidance of doubt, the field of use excludes
development, manufacture and commercialization of genetically
modified autologous T cells made by obtaining a patient's T cells
via a standard leukapheresis procedure, genetically modifying the T
cells ex vivo, expanding the T cells in cell culture, and
formulating the T cells for later administration to the patient.''
This technology discloses CAR therapies that target CD22 alone or
in combination with CD19 by utilizing the anti-CD22 binder known as
m971. CD22 and CD19 are expressed on the surface of B cells in B cell
malignancies and CAR-T utilizing binders targeting CD 19 and CD22 have
shown early promise in clinical trials for B cell malignancies.
This Notice is made in accordance with 35 U.S.C. 209 and 37 CFR
part 404. The prospective exclusive license will be royalty bearing,
and the prospective exclusive license may be granted unless within
fifteen (15) days from the date of this published Notice, the National
Cancer Institute receives written
[[Page 50897]]
evidence and argument that establishes that the grant of the license
would not be consistent with the requirements of 35 U.S.C. 209 and 37
CFR part 404.
In response to this Notice, the public may file comments or
objections. Comments and objections, other than those in the form of a
license application, will not be treated confidentially, and may be
made publicly available.
License applications submitted in response to this Notice will be
presumed to contain business confidential information and any release
of information from these license applications will be made only as
required and upon a request under the Freedom of Information Act, 5
U.S.C. 552.
Dated: September 7, 2021.
Richard U. Rodriguez,
Associate Director, Technology Transfer Center, National Cancer
Institute.
[FR Doc. 2021-19618 Filed 9-10-21; 8:45 am]
BILLING CODE 4140-01-P
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