Clinical Research Directory
Browse clinical research sites, groups, and studies.
Study to Evaluate HM15275 in Obese or Overweight Subjects Without Diabetes Mellitus
Sponsor: Hanmi Pharmaceutical Company Limited
Summary
This Study is a Phase 2 Study to Evaluate Efficacy, Safety, and Tolerability of HM15275 for 36 Weeks in Obese or Overweight Subjects Without Diabetes Mellitus.
Official title: A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel Group Study to Evaluate Efficacy, Safety, and Tolerability of HM15275 for 36 Weeks in Obese or Overweight Subjects Without Diabetes Mellitus
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
267
Start Date
2025-12-02
Completion Date
2027-01
Last Updated
2026-04-08
Healthy Volunteers
No
Interventions
HM15275
HM15275 is a sterile solution for subcutaneous injection, supplied pre-filled syringes.
Placebo of HM15275
A sterile, matching solution supplied in pre-filled syringes.
Locations (14)
ProSciento Inc
Chula Vista, California, United States
Accellacare of Duly - Duly Oak Lawn
Oak Lawn, Illinois, United States
Accellacare of McFarland
Ames, Iowa, United States
Accellacare of Cary - Cary Medical Group
Cary, North Carolina, United States
Accellacare of Hickory
Hickory, North Carolina, United States
Raleigh Medical Group, P.A.
Raleigh, North Carolina, United States
Accellacare of Piedmont - Piedmont HealthCare
Statesville, North Carolina, United States
Accellacare of Wilmington, LLC
Wilmington, North Carolina, United States
Accellacare of Winston Salem
Winston-Salem, North Carolina, United States
Accellacare of Charleston
Mt. Pleasant, South Carolina, United States
Accellacare of Bristol-PAC of Tennessee
Bristol, Tennessee, United States
Bristol-Internal Medicine and Pediatric Associates of Bristol, P.C.
Bristol, Tennessee, United States
Texas Clinical Research Institute
Arlington, Texas, United States
Velocity Clinical Research, Dallas
Dallas, Texas, United States