SBIR-STTR Award

Improved Reagents for Prostate Cancer Imaging
Award last edited on: 12/2/04

Sponsored Program
SBIR
Awarding Agency
NIH : NCI
Total Award Amount
$100,000
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Eric Holmes

Company Information

Northwest Biotherapeutics Inc (AKA: NWBT)

4800 Montgomery Lane Suite 800
Bethesda, MD 20841
   (240) 497-9024
   lkrois@nwbio.com
   www.nwbio.com
Location: Single
Congr. District: 06
County: Montgomery

Phase I

Contract Number: 1R43CA103221-01A1
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2004
Phase I Amount
$100,000
Prostate cancer is the most common cancer in men and results in the second highest cancer death rate. Effective treatment options exist for localized prostate cancer, however there are few available treatment options once the disease has spread outside the prostate. As a result, accurate diagnosis and staging is critical for effective treatment and management of the disease. Imaging for occult prostate cancer has utilized bone and CT scans with limited success. More recently, the ProstaScint scan has been utilized with improved results. The ProstaScint scan utilizes the 7E11 antibody specific for an intracellular epitope of Prostate-Specific Membrane Antigen (PSMA). Because of the inaccessibility of the epitope in live prostate cancer cells, this test is relatively insensitive as tumors must reach a size wherein a substantial portion is composed of dead or apoptotic cells for detection. In this application, we propose to conduct preclinical studies aimed at developing an improved imaging reagent utilizing monoclonal antibodies specific for extracellular PSMA epitopes. These antibodies have been shown to strongly bind to live prostatic cancer cells. Studies will be conducted to obtain preclinical data on a selected antibody, designated 3C6, specific for a protein conformational epitope that has been determined to have optimal cell and antigen binding properties to conduct a phase I clinical imaging trial. Methods for coupling of the chelator CHX-A"-DTPA to the antibody without loss in binding properties will be determined. Antibody manufactured under cGMP conditions will be analyzed for structural integrity, specificity, and potency. Biodistribution of the labeled antibody will be tested in mice bearing PSMA-expressing human prostate cancer cell tumors. Stability of the antibody in vivo and in normal human serum will be tested. Finally, general safety tests will be conducted with the final antibody product. The results will form a body of basic preclinical results to guide the next phase of this work involving clinical studies in humans. An imaging reagent utilizing antibodies capable of strong and efficient binding to live prostate cancer cells would be expected to provide dramatically improved capability compared to current methods

Thesaurus Terms:
diagnosis quality /standard, image enhancement, monoclonal antibody, neoplasm /cancer classification /staging, neoplasm /cancer diagnosis, prostate neoplasm, prostate specific antigen, reagent /indicator biomarker, chemical conjugate, contrast media, tumor antigen athymic mouse, bioimaging /biomedical imaging, guinea pig, immunoaffinity chromatography, immunocytochemistry, male

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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