[Federal Register Volume 89, Number 92 (Friday, May 10, 2024)]
[Notices]
[Page 40495]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-10198]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

National Institutes of Health


Prospective Grant of an Exclusive Patent License: Antibody-Drug 
Conjugates (ADCs) for Targeting CD56-Positive Tumors

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 McSAF Inside 
Oncology SAS (``McSAF Inside Oncology'') located in Tours, France.

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 May 28, 2024 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: Rose Freel, Ph.D., Unit Supervisor, NCI 
Technology Transfer Center, Telephone: (301) 624-1257; Email: 
[email protected].

SUPPLEMENTARY INFORMATION:

Intellectual Property

    1. United States Provisional Patent Application No. 62/199,707 
filed July 31, 2015, entitled ``Antibody-drug conjugates for targeting 
CD56-positive tumors'' [HHS Reference No. E-221-2015-0-US-01];
    2. International Patent Application No. PCT/US2016/044777 filed 
July 29, 2016, entitled ``Antibody-drug conjugates for targeting CD56-
positive tumors'' [HHS Reference No. E-221-2015-0-PCT-02]; and
    3. United States Patent No. 10,548,987 issued February 02, 2020 
(corresponding to United States Patent Application No. 15/747,620 filed 
January 25, 2018), entitled ``Antibody-drug conjugates for targeting 
CD56-positive tumors'' [HHS Reference No. E-221-2015-0-US-03].
    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 field of use may be limited to the following:
    ``The use, development, and commercialization of an antibody-drug 
conjugate (ADC) for the treatment of Merkel cell carcinoma, wherein the 
ADC utilizes any technology for attachment of the cytotoxic payload and 
has:
    (1) The CDR sequences of the m906 antibody; and
    (2) a cytotoxic payload.''
    and
    ``The use, development, and commercialization of an antibody-drug 
conjugate (ADC) for the treatment of CD56-positive cancers except 
glioblastoma, wherein the ADC:
    (1) has the CDR sequences of the m906 antibody;
    (2) has a cytotoxic payload; and
    (3) utilizes solely McSAF Inside Oncology's proprietary or 
exclusively in-licensed bioconjugation technologies for attachment of 
the linker-payload(s) to the m906 antibody.
    The E-221-2015 patent family is directed to ADCs utilizing the 
CD56-specific monoclonal antibody known as m906 and conjugated to a 
drug. The technology is intended to be used as a therapeutic for CD56-
positive cancers such as neuroblastoma, multiple myeloma, ovarian 
cancer, acute myeloid leukemia, and small cell lung cancer. The 
exclusive field of use which may be granted to McSAF Inside Oncology 
applies to only ADCs which either (1) treat Merkel Cell Carcinoma; or 
(2) use McSAF Inside Oncology's proprietary bioconjugation platform for 
attachment of the antibody to the linker-payload. Accordingly, the 
proposed scope of rights which may be conveyed under the license covers 
only a portion of the total scope of the E-221-2015 patent family and 
only a subset of the possible ADCs that incorporate the m906 antibody 
as well as the possible therapeutic applications of the ADCs.
    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: May 6, 2024.
Richard U. Rodriguez,
Associate Director, Technology Transfer Center, National Cancer 
Institute.
[FR Doc. 2024-10198 Filed 5-9-24; 8:45 am]
BILLING CODE 4140-01-P