RecruitingPhase 2NCT07205900

Study to Evaluate HM15275 in Obese or Overweight Subjects Without Diabetes Mellitus

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


Sponsor

Hanmi Pharmaceutical Company Limited

Enrollment

250 participants

Start Date

Dec 2, 2025

Study Type

INTERVENTIONAL

Conditions

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.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This Phase 2 clinical trial tests HM15275 — a new investigational weekly injection being evaluated for weight loss — in obese or overweight adults without type 2 diabetes over 36 weeks. Participants are randomized to one of five arms (different doses of HM15275 or placebo) to evaluate how well the drug reduces body weight and how safe and tolerable it is across different dosing levels. Adults aged 18–75 (19–75 in Korea) with a BMI of 30–50 (or 27–30 with at least one weight-related health condition) whose weight has been stable within the past 3 months are eligible; people with diabetes, prior obesity surgery, a history of pancreatitis, or certain heart conditions are excluded. Participation involves weekly subcutaneous (under-the-skin) injections for 36 weeks, a 6-week screening period, and a 4-week safety follow-up. This summary was prepared as patient-facing educational content using AI assistance.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGHM15275

HM15275 is a sterile solution for subcutaneous injection, supplied pre-filled syringes.

DRUGPlacebo of HM15275

A sterile, matching solution supplied in pre-filled syringes.


Locations(13)

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

Velocity Clinical Research, Dallas

Dallas, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07205900


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