| Literature DB >> 29130351 |
Terence R Flotte1, Eric Daniels2, Janet Benson3, Jeneé M Bevett-Rose2, Kenneth Cornetta4, Margaret Diggins2, Julie Johnston5, Susan Sepelak2, Johannes C M van der Loo5,6, James M Wilson5, Cheryl L McDonald7.
Abstract
Over a 10-year period, the Gene Therapy Resource Program (GTRP) of the National Heart Lung and Blood Institute has provided a set of core services to investigators to facilitate the clinical translation of gene therapy. These services have included a preclinical (research-grade) vector production core; current Good Manufacturing Practice clinical-grade vector cores for recombinant adeno-associated virus and lentivirus vectors; a pharmacology and toxicology core; and a coordinating center to manage program logistics and to provide regulatory and financial support to early-phase clinical trials. In addition, the GTRP has utilized a Steering Committee and a Scientific Review Board to guide overall progress and effectiveness and to evaluate individual proposals. These resources have been deployed to assist 82 investigators with 172 approved service proposals. These efforts have assisted in clinical trial implementation across a wide range of genetic, cardiac, pulmonary, and blood diseases. Program outcomes and potential future directions of the program are discussed.Entities:
Keywords: adeno-associated virus; clinical trial; gene therapy; lentivirus; preclinical; vector
Mesh:
Year: 2017 PMID: 29130351 PMCID: PMC5733658 DOI: 10.1089/humc.2017.170
Source DB: PubMed Journal: Hum Gene Ther Clin Dev ISSN: 2324-8637 Impact factor: 5.032