LivingGLP1
Study S000342

A Phase 1 Clinical Trial to Assess the Safety of DWRX5003 and Relative Bioavailability to DWC202502 and DWC202503 in Healthy Adult Volunteers

Registration

Registration
NCT07539415
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
RECRUITING
Enrollment
72
Start
2026-05-06
Primary completion
2026-10-27
Lead sponsor
Daewoong Pharmaceutical Co. LTD.
Conditions
Obesity & Overweight; Type 2 Diabetes
Interventions
DRUG:DWRX5003; DRUG:DWC202502; DRUG:DWC202503; OTHER:DWRX5003P
Results posted
FALSE
Individual participant data sharing
NO

Registered primary outcomes

  • AUC 0-t [Pre-dose (0 hour) up to 672 hours post-dose]
  • Cmax [Pre-dose (0 hour) up to 672 hours post-dose]

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