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A Phase 1, Placebo-Controlled, Double-Blind Study to Examine the Safety, Tolerability, and Pharmacokinetics of 500 mg KD025 Administered Twice Daily in Healthy Male and Post-Menopausal Female Subjects
Conditions
Interventions
Belumosudil mesylate
Placebo
Locations
1
United States
Investigational site
Buffalo, New York, United States
Start Date
March 28, 2014
Primary Completion Date
June 7, 2014
Completion Date
June 7, 2014
Last Updated
June 26, 2023
Lead Sponsor
Kadmon, a Sanofi Company
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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