Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PU-H71 + ruxolitinib is an investigational combination therapy consisting of PU-H71, a selective inhibitor of the epichaperome component of the molecular chaperone heat shock protein 90 (HSP90), and ruxolitinib, an oral Janus kinase (JAK) 1 and 2 inhibitor. The combination targets two critical pathways in myelofibrosis and potentially other hematological malignancies: PU-H71 disrupts oncogenic protein networks stabilized by HSP90, while ruxolitinib blocks aberrant JAK-STAT signaling in malignant hematopoietic cells. PU-H71 is being developed by Samus Therapeutics. The primary indication under study is myelofibrosis, especially in patients with inadequate response to ruxolitinib monotherapy. The combination is undergoing early-phase clinical trials to evaluate safety, tolerability, and preliminary efficacy[1][3][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 PU-H71 + ruxolitinib.