Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
BV-T829 is a preclinical gene therapy candidate developed by BioViva, a biotechnology company focused on longevity and regenerative medicine. The candidate is designed to deliver the gene for telomerase reverse transcriptase (TERT) using a viral vector, such as an adeno-associated virus (AAV) or cytomegalovirus (CMV). The primary objective of BV-T829 is to combat cellular senescence by extending telomeres, which naturally shorten as cells divide, thereby potentially treating a variety of age-related conditions and improving overall healthspan. The program is part of BioViva's early-stage portfolio aimed at cellular rejuvenation and regenerative medicine.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on BV-T829.