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NON-NATURAL AMINO ACIDS IN PEPTIDE DRUG DEVELOPMENT

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R41DA016033-01
Agency Tracking Number: DA016033
Amount: $125,279.00
Phase: Phase I
Program: STTR
Solicitation Topic Code: N/A
Solicitation Number: N/A
Timeline
Solicitation Year: N/A
Award Year: 2002
Award Start Date (Proposal Award Date): N/A
Award End Date (Contract End Date): N/A
Small Business Information
ARGOLYN BIOSCIENCE, INC. 710 JOHNNIE DODDS BLVD, STE 202
MOUNT PLEASANT, SC 29464
United States
DUNS: N/A
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 THOMAS DIX
 (843) 284-2202
 TAD@ARGOLYN.COM
Business Contact
 GILBERT PEARSON
Phone: (843) 284-2202
Email: MARSHDC@MUSC.EDU
Research Institution
 MEDICAL UNIVERSITY OF SOUTH CAROLINA
 
MEDICAL UNIVERSITY OF SOUTH CAROLINA
CHARLESTON, SC 29208
United States

 Nonprofit College or University
Abstract

Argolyn Bioscience Inc. is an early stage biotechnology company that creates novel peptide drugs and diagnostics with greatly improved intrinsic pharmaceutical properties through substitution of non-natural amino acid analogues for arginine (Arg) or lysine (Lys). In proof-of concept studies thus far, application of the Argolyn technology to peptides of therapeutic interest has resulted in dramatic increases in receptor binding, induction of receptor selectivity, blood and plasma stabilization, and delivery through the blood brain barrier (BBB). A key question for our technology is its breadth: can any peptide of biological interest be improved? The Company currently has late-discovery-stage lead candidates in psychosis, pain, and thrombosis; the psychosis and thrombosis leads are being pursued through other STTRs (submitted) and currently active grants. In this proposal, we will use ABS17, our lead candidate in pain, as another vehicle with which to evaluate the robustness of the technology. We propose to evaluate the systemic pharmacokinetics, blood brain barrier access, oral bioavailability, microsomal stability, and preliminary toxicity of ABS17. Completion of the Specific Aims of this proposal, in combination with data already accumulated on this peptide, will "round out" the preclinical work and provide a third peptide candidate on which the Argolyn platform was successfully applied. It will also lead directly into the Phase 2 STTR that will address the technology more generically (immunogenicity, toxicity of the individual non-natural amino acid residues, and model peptides containing them, etc.).

* Information listed above is at the time of submission. *

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