LivingGLP1
Study S001886

A Master Protocol to Investigate the Efficacy and Safety of LY3437943 Once Weekly in Participants With Type 2 Diabetes Mellitus Who Have Obesity or Overweight: A Randomized Double-Blind, Placebo-Controlled Trial

Registration

Registration
NCT05929079
Acronym
TRIUMPH-2
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
1152
Start
2023-07-11
Primary completion
2026-06-16
Lead sponsor
Eli Lilly and Company
Conditions
Type 2 Diabetes; Obesity; Overweight; Obstructive Sleep Apnea
Interventions
DRUG:Retatrutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:J1I-MC-GZBK; OTHER:J1I-MC-GSA2; OTHER:2023-503658-11-00; NIH:2023

Registered primary outcomes

  • Percent Change from Baseline in Body Weight [Baseline, Week 80]
  • Change from Baseline in Apnea-Hypopnea Index (AHI) for GSA2 Subset [Baseline, Week 80]

Linked records (1)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0010184Retatrutide in adults with obesity and type 2 diabetes (TRIUMPH-2): a double-blind, parallel-group, randomised, placebo-controlled, phase 3 trial.
Bellido V, Lancet (London, England)
2026Randomized trialPMID 42810372DOIcites ClinicalTrials.gov:NCT05929079; registry reference DERIVED:42810372