LivingGLP1
Study S003280

An Open-label, Randomized, Multiple-dose, Two-cycle, Two-way Crossover Phase 1 Study to Evaluate the Effect of Food on the Pharmacokinetics of CX11 Tablets in Healthy Participants

Registration

Registration
NCT07349381
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
32
Start
2026-03-04
Primary completion
2026-06-30
Lead sponsor
Vincentage Pharma Co., Ltd
Conditions
Obesity & Overweight; Type 2 Diabetes
Interventions
DRUG:CX11 (VCT220)
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • Area Under the Concentration-time curve from 0 to 24 hour (AUC0-24) of CX11 (VCT220) [Predose at Day1 up to 35 days postdose]
  • Maximum Observed Concentration (Cmax) of CX11 (VCT220) [Predose at Day1 up to 35 days postdose]
  • Time to Maximum Observed Concentration (Tmax) of CX11 (VCT220) [Predose at Day 1 up to 35 days postdose]

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