LivingGLP1
Study S003335

A Double-Blind, Randomized, Placebo-Controlled Phase 1 Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single and Multiple Doses of CT-996 in Overweight/Obese Participants and in Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT05814107
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
94
Start
2023-05-09
Primary completion
2025-11-07
Lead sponsor
Carmot Australia First Pty Ltd
Conditions
Type 2 Diabetes; Overweight or Obesity
Interventions
DRUG:CT-996; DRUG:Placebo
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Incidence of Treatment-Emergent Adverse Events [From first study drug administration until last safety follow-up (up to 31 days [Part 1] or 58 days [Parts 2 and 3])]

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