Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This entry refers to the co-administration of boceprevir and St John's Wort (Hypericum perforatum), which was evaluated in a Phase I pharmacokinetic and safety study by the St Stephens Aids Trust. Boceprevir is a small molecule NS3 protease inhibitor used for the treatment of chronic hepatitis C virus (HCV) genotype 1 infection. St John's Wort is an herbal dietary supplement commonly used to manage symptoms of depression, which is a frequent side effect of hepatitis C therapy. The study aimed to determine if St John's Wort, a known inducer of cytochrome P450 enzymes (specifically CYP3A4), would significantly alter the plasma concentrations of boceprevir. Results indicated that co-administration did not have a clinically significant effect on boceprevir levels, suggesting that the two can be safely used together.
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 boceprevir + St John's Wort.