LivingGLP1
Study S002307

A Phase 2 Randomised Controlled Study to Investigate the Efficacy and Safety of Subcutaneously Administered PG-102 for 24 Weeks Compared With Placebo and Open-Label Semaglutide in Patients With Type 2 Diabetes Mellitus

Registration

Registration
NCT07187856
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
NOT_YET_RECRUITING
Enrollment
80
Start
2026-01
Primary completion
2026-09
Lead sponsor
ProGen. Co., Ltd.
Conditions
Type 2 Diabetes Mellitus (T2DM)
Interventions
DRUG:PG-102; DRUG:Placebo; DRUG:Semaglutide
Results posted
FALSE

Registered primary outcomes

  • Absolute change in HbA1c From Baseline at Week 24 [24 weeks]

Linked records (0)

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