Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Panobinostat + docetaxel + prednisone is an experimental combination therapy evaluated for the treatment of metastatic castration-resistant prostate cancer (mCRPC). **Panobinostat** is a pan-histone deacetylase (HDAC) inhibitor that induces cell cycle arrest and apoptosis by modulating gene expression. **Docetaxel** is a taxane-class cytotoxic chemotherapeutic that inhibits microtubule depolymerization, causing cell-cycle arrest at the G2/M phase. **Prednisone** is a synthetic glucocorticoid used for its anti-inflammatory and immunosuppressive properties, and also commonly paired with docetaxel in mCRPC to reduce some side effects and possibly enhance efficacy. This combination was tested in phase I trials to determine safety and early indications of activity in castration-resistant prostate cancer, showing some preliminary evidence of PSA reduction and feasibility for further study[1][3][6].
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 panobinostat + docetaxel + prednisone.