94-5496. Prospective Grant of Exclusive and Co-Exclusive Licenses: In-Vivo Imaging and Radiotherapy Targeting Antigens Recognized by the B1, B3 and B5 Antibodies  

  • [Federal Register Volume 59, Number 47 (Thursday, March 10, 1994)]
    [Unknown Section]
    [Page 0]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 94-5496]
    
    
    [[Page Unknown]]
    
    [Federal Register: March 10, 1994]
    
    
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    DEPARTMENT OF HEALTH AND HUMAN SERVICES
     
    
    Prospective Grant of Exclusive and Co-Exclusive Licenses: In-Vivo 
    Imaging and Radiotherapy Targeting Antigens Recognized by the B1, B3 
    and B5 Antibodies
    
    AGENCY: National Institutes of Health, Public Health Services, DHHS.
    
    ACTION: Notice.
    
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    SUMMARY: This is notice in accordance with 35 U.S.C. 209(c)(1) and 37 
    CFR 404.7(a)(1)(i) that the National Institutes of Health (NIH), 
    Department of Health and Human Services, is contemplating the grant of 
    limited field of use exclusive and co-exclusive licenses in the United 
    States to practice the invention embodied in U.S. Patent Application 
    Number 07/596,289 entitled ``Antibodies Specific for Normal Primate 
    Tissue, Malignant Human Cultured Cell Lines and Human Tumors'', to 
    NeoRx Corporation, having a place of business in Seattle, WA and 
    ImmunoMedics, Inc., having a place of business in Morris Plains, New 
    Jersey. The patent rights in this invention have been assigned to the 
    United States of America.
        The prospective licenses will be royalty-bearing and will comply 
    with the terms and conditions of 35 U.S.C. 209 and 37 CFR 404.7.
        The prospective licenses may be granted unless, within 60 days from 
    the date of this published notice, NIH receives written evidence and 
    argument that establishes that the grant of the licenses would not be 
    consistent with the requirements of 35 U.S.C. 209 and 37 CFR 404.7.
        (1.) NeoRx Corporation would be granted a co-exclusive license 
    limited to the use of the monoclonal antibodies of the subject 
    invention with Tc-99m for in-vivo imaging of cancer and with Yttrium-
    90, Rhenium-186, Rhenium-188 and Iodine-125 for cancer radiotherapy. 
    NeoRx would also be granted an exclusive license limited to the use of 
    the monoclonal antibodies of the subject invention with Lutetium-177 
    and Lead-212 for cancer radiotherapy.
        (2.) ImmunoMedics, Inc. would be granted a co-exclusive license 
    limited to the use of the monoclonal antibodies of the subject 
    invention with Tc-99m for in-vivo imaging of cancer and with Yttrium-
    90, Rhenium-186, Rhenium-188 and Iodine-125 for cancer radiotherapy. 
    ImmunoMedics, Inc. would also be granted an exclusive license limited 
    to the use of the monoclonal antibodies of the subject invention with 
    Iodine-131 for cancer radiotherapy.
        The present invention relates to the monoclonal antibodies(MAb) B1, 
    B3, and B5. Of particular importance is the Mab B3 of this invention, 
    which shows strong reactivity with the Lewis-Y antigen on many human 
    solid tumors and has limited reactivity with normal human tissues. MAb 
    B3 reacts strongly with all adenocarcinomas of the colon and 75% of 
    them react strongly and homogeneously. MAb B3 has also shown similar 
    strong reactivity with other gastrointestinal malignancies such as 
    esophageal (80%) and gastric carcinomas (75%); MAb B3 reacts strongly 
    with approximately 70% of adenocarcinomas of the lung and also reacts 
    with about 40% of squamous cell carcinomas of the lung and 25% of large 
    cell carcinomas. MAb B3 reacts heterogeneously with 70% of breast 
    carcinomas and homogeneously with about 65% of adenocarcinomas of the 
    prostate and 100% of transitional cell carcinomas of the bladder. 
    Several important characteristics of MAb B3 make it an ideal candidate 
    for further development for use as an immunotoxin for treatment of 
    cancers: (1) Its strong and uniform reactivity with many human solid 
    carcinomas; (2) its limited reactivity with normal tissues and (3) the 
    fact that similar reactivity is found in normal monkey and human 
    tissues (which allow for performance of preclinical toxicology studies 
    with predictive value for a clinical trial).
    
    ADDRESSES: Request for a copy of this patent application, inquiries, 
    comments and other materials relating to the contemplated license 
    should be directed to: Mr. Daniel R. Passeri, Office of Technology 
    Transfer, National Institutes of Health, Box OTT, Bethesda, MD 20892. 
    Telephone: (301) 496-7735; Facsimile: (301) 402-0220. A signed 
    Confidentiality Agreement will be required to receive copies of the 
    patent application. Properly filed competing applications for a 
    licensee filed in response to this notice will be treated as objections 
    to the contemplated license. Only written comments and/or application 
    for a license which are received by the NIH Office of Technology 
    Transfer within sixty (60) days of this notice will be considered.
    
        Dated: March 2, 1994.
    Donald P. Christoferson,
    Acting Director, Office of Technology Transfer.
    [FR Doc. 94-5496 Filed 3-9-94; 8:45 am]
    BILLING CODE 4140-01-M
    
    
    

Document Information

Published:
03/10/1994
Department:
Health and Human Services Department
Entry Type:
Uncategorized Document
Action:
Notice.
Document Number:
94-5496
Pages:
0-0 (1 pages)
Docket Numbers:
Federal Register: March 10, 1994