Condition: Chemotherapy-induced Peripheral Neuropathy (CIPN) · Sponsor: AnHorn Medicines Co. Ltd.
This is a Phase 1, first-in-human (FIH), randomized, double-blind, placebo-controlled, parallel-group, single ascending dose (SAD) study to evaluate the safety, tolerability, and pharmacokinetics of AH-008 administered as a single intravenous infusion in healthy adult subjects. Four sequential dose cohorts will be evaluated, each with sentinel dosing and SRC-reviewed dose escalation.
This description comes directly from the study's public registry record.
Contact details are listed per location below or on the registry record.
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| ICON Clinial Research Unit | Salt Lake City, Utah, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07697560