LivingGLP1
Study S002177

A Phase 2 Dose-Finding and Proof-of-Concept Study to Evaluate the Effect on Body Composition and Safety of Enobosarm in Patients Treated With Glucagon-Like Peptide-1 (GLP-1) Receptor Agonists for Chronic Weight Management

Registration

Registration
NCT06282458
Acronym
QUALITY
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
TRIPLE
Status
COMPLETED
Enrollment
168
Start
2024-04-29
Primary completion
2025-04-11
Lead sponsor
Veru Inc.
Conditions
Muscle Loss; Obesity
Interventions
DRUG:Enobosarm; DRUG:Semaglutide
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • The primary endpoint for the study is the percentage change from baseline in total lean body mass at 112 days. [Day 112]

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
R0045473Not All Weight Loss Is Equal: Towards Muscle‐Preserving Therapies in Obesity
Joseph D Abraham, Journal of Cachexia Sarcopenia and Muscle
2026Randomized trialPMID 42046455DOIcites ClinicalTrials.gov:NCT06282458