[Federal Register Volume 84, Number 26 (Thursday, February 7, 2019)]
[Notices]
[Pages 2537-2539]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-01431]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Prospective Grant of an Exclusive Patent License: Development and
Commercialization of Cell Therapies for Cancer
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
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 Ziopharm
Oncology, Inc. (``Ziopharm''), headquartered in Boston, MA.
DATES: Only written comments and/or applications for a license which
are received by the National Cancer Institute's Technology Transfer
Center on or before February 22, 2019 will be considered.
ADDRESSES: Requests for copies of the patent applications, inquiries,
and comments relating to the contemplated Exclusive Patent License
should be directed to: Andrew Burke, Ph.D., Senior Technology Transfer
Manager, NCI Technology Transfer Center, 9609 Medical Center Drive, Rm.
1E530, MSC 9702, Bethesda, MD 20892-9702 (for business mail),
Rockville, MD 20850-9702; Telephone: (240)-276-5484; Facsimile: (240)-
276-5504; Email: [email protected].
SUPPLEMENTARY INFORMATION:
Intellectual Property
Group A
E-028-2015: Anti-Mutated KRAS T Cell Receptors
1. US Provisional Patent Application 62/084,654, filed November 26,
2014 (E-028-2015-0-US-01);
2. International Patent Application PCT/US2015/062269, filed
November 24, 2015 (E-028-2015-1-PCT-01);
3. Australian Patent Application 2015353720, filed May 18, 2017 (E-
028-2015-1-AU-02);
4. Canadian Patent Application 2968399, filed May 18, 2017 (E-028-
2015-1-CA-03);
5. Chinese Patent Application 201580070673.7, filed June 23, 2017
(E-028-2015-1-CN-04);
6. European Patent Application 15807756.0 filed June 23, 2017 (E-
028-2015-1-EP-05);
7. Israeli Patent Application 252258, filed May 14, 2017 (E-028-
2015-1-IL-06);
8. Japanese Patent Application 527874/2017, filed May 24, 2017 (E-
028-2015-1-JP-07);
9. Korean Patent Application 2017-7017289, filed June 23, 2017 (E-
028-2015-1-KR-08);
10. Mexican Patent Application MX/a/2017/006865, filed May 25, 2017
(E-028-2015-1-MX-09);
11. New Zealand Patent Application 732045, filed May 18, 2017 (E-
028-2015-1-NZ-10);
12. Saudi Arabian Patent Application 517381608, filed May 25, 2017
(E-028-2015-1-SA-11);
13. Singapore Patent Application 11201704155U, filed May 23, 2017
(E-028-2015-1-SG-12);
14. United States Utility Patent Application 15/528,813, filed May
23, 2017 (E-028-2015-1-US-13); and
15. Hong Kong Patent Application 18103250.9, filed March 7, 2018
(E-028-2015-1-HK-14).
E-180-2015: Anti-Mutated KRAS T Cell Receptors
1. US Provisional Patent Application 62/171,321, filed June 5, 2015
(E-180-2015-0-US-01).
E-265-2015: T Cell Receptors Recognizing HLA-CW8 Restricted Mutated
KRAS
1. US Provisional Patent Application 62/218,688, filed September
15, 2015 (E-265-2015-0-US-01);
2. International Patent Application PCT/US2016/050875, filed
September 9, 2016 (E-265-2015-0-PCT-02);
3. Australian Patent Application 2016323017, filed March 6, 2018
(E-265-2015-0-AU-03);
4. Canadian Patent Application 2998869, filed March 15, 2018 (E-
265-2015-0-CA-04);
5. Chinese Patent Application 201680058891.3, filed April 3, 2018
(E-265-2015-0-CN-05);
6. European Patent Application 16770408.9 filed March 7, 2018 (E-
265-2015-0-EP-06);
7. Israeli Patent Application 257840, filed March 4, 2018 (E-265-
2018-0-IL-07);
8. Japanese Patent Application 513423/2018, filed March 13, 2018
(E-265-2015-0-JP-08);
9. Korean Patent Application 2018-7010326, filed April 12, 2018 (E-
265-2015-0-KR-09);
10. Mexican Patent Application MX/a/2018/003062, filed March 12,
2018 (E-265-2015-0-MX-10);
11. New Zealand Patent Application 740714, filed March 14, 2018 (E-
265-2015-0-NZ-11);
12. Saudi Arabian Patent Application 518391109, filed March 13,
2018 (E-265-2015-0-SA-12);
13. Singapore Patent Application 11201802069U, filed March 13, 2018
(E-265-2015-0-SG-13); and
14. United States Utility Patent Application 15/758,954, filed
March 9, 2018 (E-265-2015-0-US-14).
E-175-2016: Anti-KRAS G12D T Cell Receptors
1. US Provisional Patent Application 62/369,883, filed August 2,
2016 (E-175-2016-0-US-01); and
2. International Patent Application PCT/US2017/044615, filed July
31, 2017 (E-175-2016-0-PCT-02).
E-181-2017: HLA Class II-Restricted T Cell Receptors Against Mutated
RAS
1. US Provisional Patent Application 62/560,930, filed September
20, 2017 (E-181-2017-0-US-01);
2. International Patent Application PCT/US2018/051641, filed
September 19, 2018 (E-181-2017-0-PCT-02);
3. Argentine Patent Application P180102695, filed September 20,
2018 (E-181-2017-0-AR-03);
4. Taiwan Patent Application 107133221, filed September 20, 2018
(E-181-2017-0-TW-05); and
5. United States Utility Patent Application 16/135,231, filed
September 19, 2018 (E-181-2017-0-US-06).
E-239-2017: HLA Class I-Restricted T Cell Receptors Against Mutated RAS
1. US Provisional Patent Application 62/594,244, filed December 4,
2017 (E-239-2017-0-US-01); and
2. International Patent Application PCT/US2018/063581, filed
December 3, 2018 (E-239-2017-0-PCT-02).
E-166-2018: HLA-A3-Restricted T Cell Receptors Against Mutated RAS
1. US Provisional Patent Application 62/749,750, filed October 24,
2018 (E-166-2018-0-US-01).
[[Page 2538]]
Group B
E-237-2017-0: T Cell Receptors Recognizing Mutated P53
1. US Provisional Patent Application 62/565,383, filed September
29, 2017 (E-237-2017-0-US-01); and
2. International Patent Application PCT/US2018/051285, filed
September 17, 2018 (E-237-2017-2-PCT-01).
Group C
E-098-2018: T Cell Receptors Which Recognize Mutated EGFR
1. US Provisional Patent Application 62/665,234, filed May 01, 2018
(E-098-2018-0-US-01).
Group D
E-237-2017-1: Methods of Isolating T Cells Having Antigenic Specificity
for a P53 Cancer-Specific Mutation
1. US Provisional Patent Application 62/565,464, filed September
29, 2017 (E-237-2017-1-US-01); and
2. International Patent Application PCT/US2018/051280, filed
September 17, 2018 (E-237-2017-1-PCT-02).
Group E
E-182-2017: Methods for Selectively Expanding Cells Expressing a TCR
with a Murine Constant Region
1. US Provisional Patent Application 62/568,339, filed October 5,
2017 (E-182-2017-0-US-01); and
2. International Patent Application PCT/US2018/052432, filed
September 24, 2018 (E-182-2017-0-PCT-02).
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:
Fields of Use Applying to Intellectual Property Group A
``Development, manufacture and commercialization of autologous,
peripheral blood T cell therapy products engineered by transposon-
mediated gene transfer to express T cell receptors reactive to mutated
KRAS, as claimed in the Licensed Patent Rights, for the treatment of
human cancers. Specifically excluded from this field of use are, a)
retrovirally-engineered peripheral blood T cell therapy products for
the treatment of human cancers, and b) CRISPR-engineered peripheral
blood T cell therapy products for the treatment of human cancers.
Development, manufacture and commercialization of companion
diagnostics approved or cleared by the FDA or equivalent foreign
regulatory agency for Licensee-proprietary T cell therapy products.''
Fields of Use Applying to Intellectual Property Group B
``Development, manufacture and commercialization of autologous,
peripheral blood T cell therapy products engineered by transposon-
mediated gene transfer to express T cell receptors reactive to mutated
P53, as claimed in the Licensed Patent Rights, for the treatment of
human cancers. Specifically excluded from this field of use are CRISPR-
engineered peripheral blood T cell therapy products for the treatment
of human cancers.
Development, manufacture and commercialization of companion
diagnostics approved or cleared by the FDA or equivalent foreign
regulatory agency for Licensee-proprietary T cell therapy products.''
Fields of Use Applying to Intellectual Property Group C
``Development, manufacture and commercialization of autologous,
peripheral blood T cell therapy products engineered by transposon-
mediated gene transfer to express T cell receptors reactive to mutated
EGFR, as claimed in the Licensed Patent Rights, for the treatment of
human cancers.
Development, manufacture and commercialization of companion
diagnostics approved or cleared by the FDA or equivalent foreign
regulatory agency for Licensee-proprietary T cell therapy products.''
Fields of Use Applying to Intellectual Property Group D
``Development, manufacture and commercialization of autologous,
peripheral blood T cell therapy products engineered by transposon-
mediated gene transfer to express T cell receptors reactive to mutated
P53, isolated as claimed in the Licensed Patent Rights, for the
treatment of human cancers. Specifically excluded from this field of
use are CRISPR-engineered peripheral blood T cell therapy products for
the treatment of human cancers.
Development, manufacture and commercialization of companion
diagnostics approved or cleared by the FDA or equivalent foreign
regulatory agency for Licensee-proprietary T cell therapy products.''
Fields of Use Applying to Intellectual Property Group E
``Development, manufacture and commercialization of autologous,
peripheral blood T-cell therapy products engineered by non-viral gene
transfer to express tumor-reactive T cell receptors, as claimed in the
Licensed Patent Rights, for the treatment of human cancers.
Development, manufacture and commercialization of companion
diagnostics approved or cleared by the FDA or equivalent foreign
regulatory agency for Licensee-proprietary T cell therapy products.''
Intellectual Property Group A is primarily directed to isolated T
cell receptors (TCRs) reactive to mutated Kirsten rat sarcoma viral
oncogene homolog (KRAS), within the context of several human leukocyte
antigens (HLAs). Mutated KRAS, which plays a well-defined driver role
in oncogenesis, is expressed by a variety of human cancers, including:
pancreatic, lung, endometrial, ovarian and prostate. Due to its
restricted expression in precancerous and cancerous cells, this antigen
may be targeted on mutant KRAS-expressing tumors with minimal normal
tissue toxicity.
Intellectual Property Group B is primarily directed to isolated
TCRs reactive to mutated tumor protein 53 (TP53 or P53), within the
context of several HLAs. P53 is the archetypal tumor suppressor gene
and the most frequently mutated gene in cancer. Contemporary estimates
suggest that >50% of all tumors carry mutations in P53. Because of its
prevalence in cancer and its restricted expression to precancerous and
cancerous cells, this antigen may be targeted on mutant P53-expressing
tumors with minimal normal tissue toxicity.
Intellectual Property Group C is primarily directed to isolated
TCRs reactive to mutated epidermal growth factor receptor (EGFR),
within the context of HLA DPA1*02:01 and HLA DPB1*01:01. EGFR is a
transmembrane protein involved in cell growth and proliferation
signaling. Mutations in the gene encoding EGFR can lead to its
overexpression, causing several types of cancer (e.g., non-small cell
lung cancer (NSCLC)). Because of its prevalence in certain cancers and
its restricted expression to precancerous and cancerous tissues, this
antigen may be targeted on mutant EGFR-expressing tumors with minimal
normal tissue toxicity.
Intellectual Property Group D is primarily directed to methods of
isolating T cells which are reactive to mutated P53 antigens. Briefly,
pools of 25-mer peptides covering known P53 ``hotspot'' mutations have
been generated. These peptides may be pulsed into autologous antigen
presenting cells which are subsequently co-cultured with the patient's
isolated T
[[Page 2539]]
cells. Reactive T cells are then purified and may be used as source
material for the further isolation of mutant P53-targeting TCRs.
Intellectual Property Group E is primarily directed to a method of
selectively sorting and expanding T cells which have been engineered to
stably express a murine-human hybrid TCR; a TCR wherein the human
constant region has been replaced with the corresponding murine
constant region sequences. Unlike typical OKT3 antibody-mediated cell
expansion protocols, which operate in a non-specific manner to
stimulate all T cells via the CD3 complex, the H57 antibody utilized in
the claimed method(s) binds specifically to the mouse constant region
domain of the hybrid TCR, leading to selective expansion of T cells
expressing the desired exogenous receptor.
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 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: January 30, 2019.
Richard U. Rodriguez,
Associate Director, Technology Transfer Center, National Cancer
Institute.
[FR Doc. 2019-01431 Filed 2-6-19; 8:45 am]
BILLING CODE 4140-01-P