LivingGLP1
Study S000657

A Study to Evaluate the Efficacy, Safety & Tolerability of Maridebart Cafraglutide in Adults With T2DM

Registration

Registration
NCT06660173
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
ACTIVE_NOT_RECRUITING
Enrollment
409
Start
2024-11-07
Primary completion
2025-10-06
Lead sponsor
Amgen
Conditions
Type 2 Diabetes Mellitus (T2DM)
Interventions
DRUG:Maridebart Cafraglutide; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
CTIS:2024-513539-25-00

Registered primary outcomes

  • Change From Baseline to Week 24 in Hemoglobin A1c (HbA1c) [Baseline to Week 24]

Linked records (0)

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