SBIR-STTR Award

Monoclonal antibody conjugates for therapy and diagnosis
Award last edited on: 1/30/14

Sponsored Program
SBIR
Awarding Agency
NIH : NCI
Total Award Amount
$300,000
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
Raymond J Kelleher

Company Information

T & B Bioclone

4786 Enser Road
Eden, NY 14057
   (716) 992-2633
   nejat.egilmez@louisville.edu
   N/A
Location: Single
Congr. District: 27
County: Erie

Phase I

Contract Number: N44CM087779-000
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
1988
Phase I Amount
$50,000
Monoclonal antibodies specific for a human lung tumor-associated glycoprotein antigen (gp160) will be used to develop and test a cytotoxic drug delivery system for therapy of cancer patients and to develop simple diagnostic/ prognostic immunoassays. The gp-160 is a membrane-associated glycoprotein that is found in significant levels on several major types of human lung tumors including squamous cell carcinomas, adenocarcinomas, and large cell tumors. The specificity of a monoclonal antibody (5E8) for the tumor-associated antigen has been established. The proposed therapeutic exploitation involves covalent coupling of these monoclonal antibodies to unilamellar liposomes that are filled with a cytotoxic drug. Recent advances in the preparation of liposomes have been made and the successful therapeutic exploitation of such immunospecific liposomes has been established in a mouse tumor model.Phase I of this proposal will include 1. preparation of gp-l60-specific drug-containing liposomes, 2. a test of the ability of immunospecific liposomes to kill gp-160-positive human lung tumors selectively in vitro, 3. generation and purification of 2S50 grams of gp-l60-specific antibodies, and 4. establishment of simple and sensitive immenoassays for detecting circulating gp160 or anti-gp-160 in lung tumor patients.The ultimate goal of Phase I is to establish a rationale for testing the immunospecific liposomes for their ability to selectively deliver diagnostic and/or cytotoxic agents to a tumor site in the patient and to produce tumor killing in excess of that induced by either antibody or cytotoxic agent alone. It is expected that clinical trials can begin as soon as selective killing with the liposomes is established in vitro and gram quantities of antibody are available.National Cancer Institute (NCI)

Phase II

Contract Number: N44CM087779-001
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
1989
Phase II Amount
$250,000
No Abstract Available

Thesaurus Terms:
Immunity, Immunotherapy Immunological Preparations, Monoclonal AntibodiesNational Cancer Institute (NCI)