LivingGLP1
Study S002127

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of Retatrutide Once Weekly in Participants Who Have Obesity or Overweight and Chronic Low Back Pain

Registration

Registration
NCT07035093
Acronym
TRIUMPH-7
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
DOUBLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
586
Start
2025-05-29
Primary completion
2027-09
Lead sponsor
Eli Lilly and Company
Conditions
Obesity; Overweight; Chronic Low Back Pain (CLBP)
Interventions
DRUG:Retatrutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:J1I-MC-GZQD; CTIS:2024-517431-43-00

Registered primary outcomes

  • Change from Baseline in Pain Intensity Per Numeric Rating Scale [Baseline, up to 72 weeks]
  • Percent Change from Baseline in Body Weight [Baseline, up to 72 weeks]

Linked records (0)

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