Clinical Trial

Study of Single and Multiple Oral Doses of SCB0020160 in Healthy Adult Male Subjects

Not Yet Recruiting Phase 1
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Summary
This study aims to evaluate the safety, tolerability, pharmacokinetics, and food effect of a new investigational medicine called SCB0020160 in healthy adult men. This is the first time SCB0020160 will be administered to humans. Healthy adult men aged 18 to 65 years who meet the study eligibility criteria. Study details Participants will be randomly assigned to receive either SCB0020160 or placebo. The study includes single-dose and multiple-dose treatment periods, as well as an assessment of the effect of food on the absorption of SCB0020160. Participants will undergo safety assessments including physical examinations, vital signs, ECGs, blood and urine tests, and monitoring of adverse events. The study will also assess how SCB0020160 is processed by the body. There is no direct health benefit expected from participation. The results may help determine safe dose levels and support future clinical development of SCB0020160.
Trial Details
NCT Number NCT07682337
Lead Sponsor SCBIO Inc.
Conditions Solid Tumor, Obesity, Idiopathic Pulmonary Fibrosis
Enrollment 74 participants
Start Date 2026-06-29
Primary Completion 2027-06-01 (estimated)
Study Completion 2027-07-01 (estimated)
Updated on ClinicalTrials.gov 2026-07-02