Prospective Grant of an Exclusive Patent License: “Treatment of Acute Lymphoblastic Leukemia, T-Cell Lymphoma, and Non-Small Cell Lung Cancer Using the 4A10 Antibody and Fragments Thereof”, 4492 [2019-02442]
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Federal Register / Vol. 84, No. 32 / Friday, February 15, 2019 / Notices
Microbiology and Infectious Diseases
Research, National Institutes of Health, HHS)
Dated: February 11, 2019.
Natasha Copeland,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2019–02424 Filed 2–14–19; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Prospective Grant of an Exclusive
Patent License: ‘‘Treatment of Acute
Lymphoblastic Leukemia, T-Cell
Lymphoma, and Non-Small Cell Lung
Cancer Using the 4A10 Antibody and
Fragments Thereof’’
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
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
Patent Applications listed in the
Supplementary Information section of
this notice to Fannin Partners L.L.C.,
(‘‘Fannin’’) of Houston, Texas.
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 March 4, 2019 will be
considered.
ADDRESSES: Requests for copies of the
patent application, inquiries, and
comments relating to the contemplated
an Exclusive Patent License should be
directed to: Lauren Nguyen-Antczak, Sr.
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)–276–5530;
Facsimile: (240)-276–5504 Email:
lauren.nguyen-antczak@nih.gov.
SUPPLEMENTARY INFORMATION:
khammond on DSKBBV9HB2PROD with NOTICES
SUMMARY:
Intellectual Property
Entitled ‘‘IL–7R-alpha Specific
Antibodies for Treating Acute
Lymphoblastic Leukemia’’
(1) U.S. Provisional Patent
Application No. 62/238,612, filed
October 7, 2015, corresponding to NIH
Ref. No. E–247–2015/0–US–0;
(2) International Patent Application
No. PCT/US2016/055957, filed October
7, 2016, corresponding to NIH Ref. No.
E–247–2015/0–PCT–02;
VerDate Sep<11>2014
19:41 Feb 14, 2019
Jkt 247001
(3) Australian Patent Application No.
2016–335750, filed October 7, 2016,
corresponding to NIH Ref. No. E–247–
2015/0–AU–03;
(4) Canadian Patent Application No.
2997809, filed October 7, 2016,
corresponding to NIH Ref. No. E–247–
2015/0–CA–04;
(5) European Patent Application No.
16784678.1, filed October 7, 2016,
corresponding to NIH Ref. No. E–247–
2015/0–EP–05;
(6) U.S. Patent Application No. 15/
760,193, filed March 14, 2018,
corresponding to NIH Ref. No. E–247–
2015/0–US–07;
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 where patent
applications are filed and the field of
use may be limited to ‘‘Treatment of
acute lymphoblastic leukemia, T-cell
lymphoma, and non-small cell lung
cancer using the 4A10 antibody and
fragments thereof’’. Additional
licensable fields of use are available.
The subject technology is directed to
monoclonal antibodies (mAb) specific
for the alpha chain of the interleukin 7
receptor (IL–7Ra), and corresponding
antigen binding fragments, bispecific
antibodies, antibody drug conjugates,
and encoding nucleic acid thereof.
Specifically developed mAbs include
those called ‘‘4A10’’ and ‘‘2B8’’. In
certain embodiments, the 4A10
antibody can be administered to treat
acute lymphoblastic leukemia,
particularly those that arise from
aberrations in T-cell lineages.
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 in these license
applications will be made only as
required and upon a request under the
PO 00000
Frm 00061
Fmt 4703
Sfmt 4703
Freedom of Information Act, 5 U.S.C.
552.
Dated: February 6, 2019.
Richard U. Rodriguez,
Associate Director, Technology Transfer
Center, National Cancer Institute.
[FR Doc. 2019–02442 Filed 2–14–19; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Office of The Director, National
Institutes of Health; Notice of Meeting
Pursuant to section 10(a) of the
Federal Advisory Committee Act, as
amended, notice is hereby given of a
meeting of the Advisory Committee to
the Director, National Institutes of
Health.
The meeting will be open to the
public, with attendance limited to space
available. Individuals who plan to
attend and need special assistance, such
as sign language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the meeting.
Name of Committee: Advisory Committee
to the Director, National Institutes of Health.
Date: June 13, 2019.
Time: 9:00 a.m. to 5:30 p.m.
Agenda: NIH Director’s Report, ACD
Working Group Reports, Other Business of
the Committee.
Place: National Institutes of Health,
Natcher Building, Conference Room D, 45
Center Drive, Bethesda, MD 20892.
Name of Committee: Advisory Committee
to the Director, National Institutes of Health.
Date: June 14, 2019.
Time: 9:00 a.m. to 1:00 p.m.
Agenda: ACD Working Group Reports,
Other Business of the Committee.
Place: National Institutes of Health,
Natcher Building, Conference Room D, 45
Center Drive, Bethesda, MD 20892.
Contact Person: Gretchen Wood, Staff
Assistant, National Institutes of Health,
Office of the Director, One Center Drive,
Building 1, Room 126, Bethesda, MD 20892,
301–496–4272, Woodgs@od.nih.gov.
Name of Committee: Advisory Committee
to the Director, National Institutes of Health
Date: December 12, 2019.
Time: 9:00 a.m. to 5:30 p.m.
Agenda: NIH Director’s Report, ACD
Working Group Reports, Other Business of
the Committee.
Place: National Institutes of Health,
Natcher Building, Conference Room D, 45
Center Drive, Bethesda, MD 20892.
Name of Committee: Advisory Committee
to the Director, National Institutes of Health.
Date: December 13, 2019.
Time: 9:00 a.m. to 1:00 p.m.
Agenda: ACD Working Group Reports,
Other Business of the Committee.
E:\FR\FM\15FEN1.SGM
15FEN1
Agencies
[Federal Register Volume 84, Number 32 (Friday, February 15, 2019)]
[Notices]
[Page 4492]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-02442]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Prospective Grant of an Exclusive Patent License: ``Treatment of
Acute Lymphoblastic Leukemia, T-Cell Lymphoma, and Non-Small Cell Lung
Cancer Using the 4A10 Antibody and Fragments Thereof''
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 Patent Applications listed in the
Supplementary Information section of this notice to Fannin Partners
L.L.C., (``Fannin'') of Houston, Texas.
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 March 4, 2019 will be considered.
ADDRESSES: Requests for copies of the patent application, inquiries,
and comments relating to the contemplated an Exclusive Patent License
should be directed to: Lauren Nguyen-Antczak, Sr. 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)-276-5530; Facsimile: (240)-
276-5504 Email: lauren.nguyen-antczak@nih.gov.
SUPPLEMENTARY INFORMATION:
Intellectual Property
Entitled ``IL-7R-alpha Specific Antibodies for Treating Acute
Lymphoblastic Leukemia''
(1) U.S. Provisional Patent Application No. 62/238,612, filed
October 7, 2015, corresponding to NIH Ref. No. E-247-2015/0-US-0;
(2) International Patent Application No. PCT/US2016/055957, filed
October 7, 2016, corresponding to NIH Ref. No. E-247-2015/0-PCT-02;
(3) Australian Patent Application No. 2016-335750, filed October 7,
2016, corresponding to NIH Ref. No. E-247-2015/0-AU-03;
(4) Canadian Patent Application No. 2997809, filed October 7, 2016,
corresponding to NIH Ref. No. E-247-2015/0-CA-04;
(5) European Patent Application No. 16784678.1, filed October 7,
2016, corresponding to NIH Ref. No. E-247-2015/0-EP-05;
(6) U.S. Patent Application No. 15/760,193, filed March 14, 2018,
corresponding to NIH Ref. No. E-247-2015/0-US-07;
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 where patent
applications are filed and the field of use may be limited to
``Treatment of acute lymphoblastic leukemia, T-cell lymphoma, and non-
small cell lung cancer using the 4A10 antibody and fragments thereof''.
Additional licensable fields of use are available.
The subject technology is directed to monoclonal antibodies (mAb)
specific for the alpha chain of the interleukin 7 receptor (IL-
7R[alpha]), and corresponding antigen binding fragments, bispecific
antibodies, antibody drug conjugates, and encoding nucleic acid
thereof. Specifically developed mAbs include those called ``4A10'' and
``2B8''. In certain embodiments, the 4A10 antibody can be administered
to treat acute lymphoblastic leukemia, particularly those that arise
from aberrations in T-cell lineages.
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 in 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: February 6, 2019.
Richard U. Rodriguez,
Associate Director, Technology Transfer Center, National Cancer
Institute.
[FR Doc. 2019-02442 Filed 2-14-19; 8:45 am]
BILLING CODE 4140-01-P