RecruitingPhase 1

Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of BGM0504 Tablets in Non-diabetic Overweight or Obese Adult Subjects

United States80 participantsStarted 2025-08-11

Plain-language summary

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.

Who can participate

Age range18 Years – 65 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Between ≥ 30.0 kg/m2 and ≤ 40.0 kg/m2 (obese); OR
✓. Between ≥ 27.0 kg/m2 and \< 30.0 kg/m2 (overweight) with at least 1 of the following: One or more symptoms of prediabetes (impaired fasting plasma glucose and/or abnormal glucose tolerance), grade 1 hypertension, simple fatty liver or dyslipidemia

What they're measuring

Number of treatment adverse events

Timeframe: 11 weeks

Trial details

NCT IDNCT07166081

SponsorBrightGene Bio-Medical Technology Co., Ltd.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2026-01-12

Contact for this trial

MB ChB

240-673-0900 mohamed.al-ibrahim@pharmaron.com

View on ClinicalTrials.gov More Non-diabetic Overweight or Obese trials