Condition: Acne · Sponsor: Sagimet Biosciences Inc.
This is a 4-part study. Part A will be a randomized, double-blind, placebo-controlled investigation of single ascending doses (SAD) to assess the safety, tolerability, pharmacokinetics (PK), and pharmacodynamic (PD) biomarkers of TVB-3567 administered orally in healthy participants. Part B will be a randomized, open-label, 2-way crossover investigation to assess the effect of food on a single dose TVB-3567 administered orally in healthy participants. Parts C and D will be randomized, double-blind, placebo-controlled investigations of multiple ascending doses (MAD) to assess the safety, tolerability, PK, and PD/biomarkers of TVB-3567 administered orally in healthy participants without and with moderate to severe acne, respectively.
This description comes directly from the study's public registry record.
Study Director · (650) 561-8600 · SB3567-CLIN-001@sagimet.com
Always discuss trial participation with your own doctor first.
| Celerion, Inc. | Tempe, Arizona, United States | Completed |
| Nucleus Network | Melbourne, Victoria, Australia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06989840