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Pharm/Tox


The NGVB provides a Pharm/Tox database to research associates as well as archiving of Pharm/Tox samples. If you know which type of service you'd like to request see below:


Pharm/Tox Database

Pharm/Tox Database

An informational Pharm/Tox database as a resource to gene therapy investigators. The database contains information on animal studies that have been conducted to study the biodistribution of vector to different target organs and to evalutate potential toxic effects associated with the use of various vector systems. Studies within the database have been submitted to the US FDA in support of gene therapy clinical trials. The purpose of the database is to inform gene therapy investigators about the conclusions of prior toxicology studies and to facilitate the cross-referencing of relevant studies in support of new Investigational New Drug Applications (INDs) applications.

Database

Pharm/Tox Archiving

Pharm/Tox Archiving

Pharmacology and Toxicology Archive. If you have performed Pharm/Tox studies submitted to the FDA and have material that must be maintained under GLP conditions, the NGVB will store the samples at no cost to academic investigators. All we ask is that your study be summarized in the NGVB Pharm/Tox database.

Request Archiving Services

Archiving

Archiving

Clinical Trial Samples. Clinical trial samples collected during post-trial monitoring can be sent and stored in the Indiana University Biorepository at no cost to the investigator.

Clinical Grade Vector, Cell Lines, and Clinical Study Samples. The NGVB will also store reserve or back-up clinical grade vector, master cell banks, and clinical study samples. This will insure that should a catastrophic event occur at the investigators current storage site, additional material would be available at the NGVB.

Request Archiving Services

For questions please contact the NGVB Manager:

NGVB Manager
317-274-4519
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