Chronic Weight Management

4

Review clinical trials related to Chronic Weight Management. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Study of Once-daily Oral ASC30 to Evaluate the Efficacy and Safety in Adult Participants With Obesity or Overweight With Type 2 Diabetes

Study ASC30-302 (AURORA-2) 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 and T2DM.

Participants needed: 1,560
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Ascletis Pharma (China) Co., LimitedUpdated: Aug 14, 2026Locations: 136
Eligibility criteria

Participant must be ≥18 years of age inclusive, or the legal age of consent in t... [+3]

Have Type 1 Diabetes Mellitus (T1DM), history of ketoacidosis or hyperosmolar st... [+6]

Status: Recruiting

A Study of Once-daily Oral ASC30 to Evaluate the Efficacy and Safety in Adult Participants With Obesity or Overweight With Weight-Related Comorbidities

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.

Participants needed: 3,003
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Ascletis Pharma (China) Co., LimitedUpdated: Aug 14, 2026Locations: 120
Eligibility criteria

Participant must be ≥18 years of age inclusive, or the legal age of consent in t... [+5]

Have any prior diagnosis of diabetes mellitus (T1DM or T2DM), or any other types... [+6]

Status: Recruiting

Efficacy and Safety of Aleniglipron in Participants With Obesity or Overweight With a Weight-Related Comorbidity (ACCOMPLISH-1)

Study GSBR-1290-12 is a Phase 3 pivotal, multicenter, global, randomized, placebo-controlled, double-blind study to investigate the long-term efficacy, safety, and tolerability of 3 maintenance doses of aleniglipron once daily (QD) compared with placebo, when used in combination with a reduced-calorie diet and increased physical activity. All participants will be randomized to at least 76 weeks of treatment to evaluate the effects on long term body weight changes, tolerability, and safety. In addition, the study will compare the effects between aleniglipron and placebo on blood pressure (BP), lipid parameters, patient-reported outcomes.

Participants needed: 3,600
Trial details
Phase: Phase 3Age: 18-79Biological sex: AllType: InterventionalSponsor: Gasherbrum Bio, Inc., a wholly owned subsidiary of Structure TherapeuticsUpdated: Aug 10, 2026Locations: 71
Eligibility criteria

Signed informed consent [+1]

Previously documented diagnosis of type 1 diabetes, type 2 diabetes, or any othe... [+6]

Status: Recruiting

A Study of Aleniglipron in Adults With Obesity or Overweight and Type 2 Diabetes Mellitus (ACCOMPLISH-2)

This is randomized, double-blind, placebo-controlled study of the long-term efficacy, safety, and tolerability of multiple doses of aleniglipron in participants living with overweight or obesity and T2DM. Participants will be randomized to aleniglipron or placebo for a total of 76 weeks of treatment.

Participants needed: 1,100
Trial details
Phase: Phase 3Age: 18-79Biological sex: AllType: InterventionalSponsor: Gasherbrum Bio, Inc., a wholly owned subsidiary of Structure TherapeuticsUpdated: Aug 10, 2026Locations: 74
Eligibility criteria

Signed Informed Consent [+2]

Have type 1 diabetes, history of ketoacidosis or hyperosmolar state/coma, or any... [+4]