Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Brentuximab vedotin + chidamide is a combination therapy regimen being evaluated for the treatment of CD30-positive peripheral T-cell lymphoma (PTCL). The regimen consists of brentuximab vedotin, an antibody-drug conjugate (ADC) that targets CD30-expressing cells to deliver the cytotoxic microtubule-disrupting agent monomethyl auristatin E (MMAE), and chidamide (tucidinostat), an orally available, subtype-selective histone deacetylase (HDAC) inhibitor. Preclinical studies suggest that chidamide synergistically enhances the apoptotic effects of brentuximab vedotin. This specific combination is being studied by The First Affiliated Hospital of Soochow University as an induction and consolidation therapy, followed by chidamide maintenance, particularly for patients who are unfit for standard chemotherapy.
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 brentuximab vedotin + chidamide.