LivingGLP1
Study S003276

A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multiple-Center Study to Evaluate the Efficacy, Safety, and Tolerability of CT-868 Administered for 26 Weeks to Overweight and Obese Participants With Type 2 Diabetes Mellitus

Registration

Registration
NCT05110846
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
103
Start
2022-02-22
Primary completion
2023-02-28
Lead sponsor
Carmot Therapeutics, Inc.
Conditions
Obesity; Overweight; Type 2 Diabetes Mellitus
Interventions
DRUG:Placebo; DRUG:CT-868
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:BP45664

Registered primary outcomes

  • Change from Baseline in Glycated Hemoglobin A1c (HbA1c) at Week 26 [Baseline and Week 26]

Linked records (0)

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