Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
docetaxel + hydroxychloroquine is a combination therapy investigated for the treatment of metastatic hormone-refractory prostate cancer. Docetaxel is a taxane-based antineoplastic agent that promotes the assembly of tubulin into stable microtubules and inhibits their disassembly, leading to a marked decrease in free tubulin and the inhibition of mitotic cell division. Hydroxychloroquine is a 4-aminoquinoline derivative that acts as an autophagy inhibitor by increasing lysosomal pH and preventing the fusion of autophagosomes with lysosomes. The rationale for the combination is that inhibiting autophagy may overcome resistance mechanisms in prostate cancer cells, thereby enhancing the cytotoxic effects of docetaxel. This specific regimen was evaluated in a Phase II clinical trial sponsored by the University of Medicine and Dentistry of New Jersey.
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 docetaxel + hydroxychloroquine.