GENE THERAPY RESOURCE PROGRAM (GTRP) Header
GENE THERAPY RESOURCE PROGRAM (GTRP) Header
HIGHLIGHTS
RSA Submissions are Accepted on a Continuous Basis

»
 Instructions for Submitting
  an RSA

» RSA Review Process
INFORMATION CENTER

» Regulatory Guidelines

» GTRP Presentations at the
  ASGT Meeting May 28, 2008

» NHLBI Home

The GTRP Steering Committee is comprised of the Chair (appointed by the NHLBI Gene Therapy Group), the Principal Investigators of the GTRP Clinical Coordinating Center and each of the GTRP Core Laboratories, the leader of the NHLBI Gene Therapy Group, members appointed by the NHLBI Gene Therapy Group with specific scientific expertise relevant to GTRP activities, representatives of the U.S. Food and Drug Administration (FDA) and a representative of the NIH Office of Biotechnology Activities (OBA).  The committee chair may request that others serve as expert consultants on an ad hoc basis. 

The GTRP Steering Committee reviews Request for Service Application (RSA) submissions and the assessments provided by the Scientific Review Board and recommends to the NHLBI Gene Therapy Group disposition of RSAs for:

  • Clinical Vector Production Services
  • Pharmacology/Toxicology Testing
  • Clinical Trial Funding Assistance

The Steering Committee meets twice a year to review RSA submissions and conducts business via conference calls.

In addition, the Steering Committee reviews program Standard Operating Procedures and provides oversight of monitoring of clinical protocols that are partially funded through the GTRP. 

» Steering Committee Roster

» Conflict of Interest Statement
  (for SC members)

login button

Login for the Steering Committee Members to access RSA and FA forms, review forms and instructions, upcoming Steering Committee Meetings, summaries of Steering Committee Meetings, the Manual of Operations, and the GTRP directory