Condition: Non-diabetic Overweight or Obese · Sponsor: BrightGene Bio-Medical Technology Co., Ltd.
This is a Phase 1, single-center, randomized, placebo-controlled, ascending dose study. The study will evaluate the pharmacokinetics (PK), pharmacodynamic (PD), preliminary efficacy, safety and tolerability of BGM0504 following daily oral administrations in non-diabetic overweight or obese adult subjects.
This description comes directly from the study's public registry record.
MB ChB · 240-673-0900 · mohamed.al-ibrahim@pharmaron.com
Always discuss trial participation with your own doctor first.
| Pharmaron CPC, Inc | Baltimore, Maryland, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07166081