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Not Yet RecruitingNCT07187856

Phase 2 Randomized Study of PG-102 vs Placebo and Semaglutide in Type 2 Diabetes Mellitus

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

Status
Not Yet Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
ProGen. Co., Ltd. · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Phase 2 Randomized Study of PG-102 vs Placebo and Semaglutide in Type 2 Diabetes Mellitus

Conditions

Interventions

TypeNameDescription
DRUGPG-102PG-102 is administered subcutaneously once weekly with a titration regimen.
DRUGPlaceboPlacebo is administered subcutaneously once weekly.
DRUGSemaglutideOpen-label semaglutide is administered subcutaneously once weekly with titration regimen.

Timeline

Start date
2026-01-01
Primary completion
2026-09-01
Completion
2026-12-01
First posted
2025-09-23
Last updated
2025-09-23

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT07187856. Inclusion in this directory is not an endorsement.

Phase 2 Randomized Study of PG-102 vs Placebo and Semaglutide in Type 2 Diabetes Mellitus (NCT07187856) · Clinical Trials Directory