All therapiesEvidence snapshot 2026-09-13
Weight & glucose

BGM0504

Activates both GLP-1 and GIP receptors.

At a glance

Selected evidence in this atlas
Studied use & population

Chinese adults with overweight or obesity without diabetes

Study context
Approval & development

China weight-management NDA acceptance announced June 11, 2026, following positive phase 3 results; no marketing approval verified.

Status sourceStatus & indications
Selected efficacy evidence

19.2% reported weight loss · 3.1% loss with placebo · 52 weeks

BGM0504-III-WL · Phase 3 · sponsor · 15 mg once weekly · Other / incompletely specified

Evidence & limitations
Important safety context

15 mg AE discontinuation 0.7%; GI events mainly mild/moderate; no hypoglycemia reported.

Safety context
Next milestone

A next milestone is not summarized for this therapy.

Milestone details

Study results apply to their own population, dose and analysis. They do not establish a ranking between therapies.

Evidence in the atlas

2 results

Each result belongs to its own study population, dose and analysis. Open a result for its chart, comparator, safety findings and limitations.

Weight loss

BGM0504-III-WL

19.2% reported weight loss · 3.1% loss with placebo · 52 weeks

15 mg once weekly

Chinese adults with overweight or obesity without diabetes

Full analysis set/total randomized population; intercurrent-event strategy not disclosed. China weight-management NDA acceptance announced June 11, 2026, following positive phase 3 results; no marketing approval verified.

Safety context

15 mg AE discontinuation 0.7%; GI events mainly mild/moderate; no hypoglycemia reported.

Limitations: 19.3% headline is per-protocol; use 19.2% FAS. HKEX filing confirms52-week duration.

Glucose control

BGM0504-IIa-T2DM

2.48 percentage-point HbA1c decrease · 0.28 pp increase with Pooled placebo · 18 weeks

15 mg weekly after six weeks of escalation

Chinese adults aged 18–65 with type 2 diabetes; BMI 19.5–35 kg/m²

ANCOVA with baseline adjustment in participants with evaluable PD data and no major relevant protocol deviations; missing data handled by LOCF.

Safety context

At 15 mg, diarrhea occurred in 9/12 and abdominal distension in 3/12; no hypoglycemia recorded.

Limitations: Small trial. The paper labels the result week 12 of target-dose administration; plotted week18 includes six titration weeks. Pooled placebo combines cohorts with different titration durations.

Biology & identity

Status in this atlas: China weight-management NDA acceptance announced June 11, 2026, following positive phase 3 results; no marketing approval verified. Status source

Hormone activity

Activates both GLP-1 and GIP receptors.

No approved trade name verified. BGM0504 is a development code; the accepted Chinese application does not itself establish marketing approval.

BrightGene Bio-Medical Technology · Originator and developer through its wholly owned Suzhou pharmaceutical subsidiary; planned sole Chinese marketing-authorization holder.; China Resources Sanjiu · Joint development and commercialization partner for the injection in Mainland China.

Uses, doses and availability depend on the formulation, indication and country. Study doses below describe research; they are not prescribing instructions.

The molecule

Activates both GLP-1 and GIP receptors.
Structure not yet verified

Structure not verified

Activates both GLP-1 and GIP receptors.

Shown: Peptide drug

An exact-drug structure was not verified in this review. The named PubChem lookup did not return a compound record; no related hormone or analogue is substituted.

BGM0504

Development timeline

Next milestone

A next milestone is not summarized for this therapy. This does not mean development has ended.

Development history3 selected milestones

BGM0504 · compound history across indications

Selected milestones only. Earlier studies may be missing; the first listed date should not be interpreted as the start of development.

  1. China Resources Sanjiu partnership

    The companies agreed to collaborate on further Mainland-China development and commercialization of BGM0504 injection.

    Source
  2. Phase 3 obesity results announced

    The trial met its primary endpoint; 15 mg produced 19.2% loss in the full analysis set at 52 weeks.

    Source
  3. Obesity NDA acceptance announced

    BrightGene announced Chinese regulatory acceptance of the injection's weight-management application.

    Source

Selected sources checked Sep 13, 2026. This is not an exhaustive history.