LivingGLP1
Study S003245

A Phase 2, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of CT-868 Administered for 16 Weeks to Overweight and Obese Adult Participants With Type 1 Diabetes Mellitus

Registration

Registration
NCT06062069
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
QUADRUPLE
Status
COMPLETED
Enrollment
111
Start
2023-10-19
Primary completion
2025-07-09
Lead sponsor
Carmot Therapeutics, Inc.
Conditions
Overweight; Obese; Type 1 Diabetes Mellitus
Interventions
DRUG:CT-868; DEVICE:CT-868 Pen Injector; DRUG:CT-868 Pen Injector, Placebo
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Compare the effect of CT-868 versus placebo on change in HbA1c (%) from baseline [at Day 1 to Week 16]

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