Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**fedratinib + rifampin** is a combination of fedratinib, an oral small molecule inhibitor of Janus kinase 2 (JAK2), and rifampin, a strong CYP3A4 inducer and antibiotic. Fedratinib is primarily indicated for intermediate-2 or high-risk primary or secondary myelofibrosis. Rifampin is commonly used to treat tuberculosis and as a prophylactic against Neisseria meningitidis carriage. When administered together, rifampin substantially decreases fedratinib plasma concentrations (by approximately 81%), due to enhanced hepatic metabolism via CYP3A4 induction, effectively compromising fedratinib's therapeutic efficacy. No therapeutic indication exists for their combination; instead, this combination is studied primarily for drug-drug interaction assessment, and its use is contraindicated or avoided in clinical practice[1][3][4][5].
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 fedratinib + rifampin.