Study #2022-0225
A Phase 1a/1b, multicenter, open-label, first-in-human study to evaluate the safety, tolerability, pharmacokinetics, and efficacy of YL201 as a single agent and in combination with other anti-cancer therapies in patients with advanced solid tumors
MD Anderson Study Status
Enrolling
Treatment Agent
Description
Resources and Links
Phone Number: 1-877-MDA-6789
Information and next steps
Disease:
Study phase:
Physician name:
Siqing Fu
Department:
Investigational Cancer Therapeutics
For general questions about clinical trials:
1-877-632-6789
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