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A Study of Once-daily Oral ASC30 to Evaluate the Efficacy and Safety in Adult Participants With Obesity or Overweight With Weight-Related Comorbidities
Condition: Obesity or Overweight With Weight-Related Comorbidities · Chronic Weight Management · Sponsor: Ascletis Pharma (China) Co., Limited
About this study
Study ASC30-301 (AURORA-1) is a Phase III, global, multicenter, randomized, double-blind, placebo-controlled study to investigate the long-term efficacy, safety, and tolerability of three maintenance doses of once-daily oral ASC30 compared with placebo in participants with obesity or overweight without T2DM.
This description comes directly from the study's public registry record.
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Source record: clinicaltrials.gov/study/NCT07743463