Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Telbivudine is an oral antiviral drug classified as a nucleoside analogue and specifically a thymidine nucleoside analogue. It inhibits hepatitis B virus (HBV) replication by acting as a selective inhibitor of HBV DNA polymerase (reverse transcriptase), leading to chain termination during viral DNA synthesis. Telbivudine is used for the treatment of chronic hepatitis B infection in adults and adolescents with evidence of active viral replication and either persistent elevations in serum aminotransferases or histologically active disease. While it can reduce HBV levels, it does not cure hepatitis B or prevent its complications such as cirrhosis or liver cancer, nor does it prevent transmission to others[1][4][5][6]. Telbivudine was developed by Novartis and marketed under the brand name Tyzeka but has been discontinued in some markets including the United States[1].
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 telbivudine.