Clinical Trial

Study of SIR2501 in Solid Tumor Patients Receiving Paclitaxel

Not Yet Recruiting Phase 2
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Summary
This Phase 2, open-label study will evaluate the safety, tolerability, and pharmacokinetics of SIR2501 in adults with solid tumors who are scheduled to receive paclitaxel-based chemotherapy. The study will also explore whether SIR2501 has the potential to reduce the development of chemotherapy-induced peripheral neuropathy (CIPN).
Trial Details
NCT Number NCT07765446
Lead Sponsor Sironax USA, Inc.
Conditions Chemotherapy-induced Peripheral Neuropathy
Enrollment 18 participants
Start Date 2026-08-03
Primary Completion 2027-12-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-08-14