Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Paclitaxel + amifostine is a combination chemotherapy regimen investigated by the State University of New York - Upstate Medical University for the treatment of recurrent or refractory solid tumors. The regimen utilizes paclitaxel, a taxane that stabilizes microtubules to induce cell cycle arrest and apoptosis, in a weekly dose-escalated schedule. Amifostine is administered as a cytoprotective agent; it is a thiophosphate prodrug converted by alkaline phosphatase into an active thiol metabolite (WR-1065) that scavenges free radicals generated by chemotherapy. This scavenging action protects normal cells from toxicity, potentially allowing for higher doses of paclitaxel to be tolerated without increasing systemic side effects. This Phase I study specifically evaluated the safety and effectiveness of this combination in patients who had failed prior therapies.
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 paclitaxel + amifostine.