NCT07205900Active, not recruitingPhase 2
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
Source: ClinicalTrials.gov · Last updated 8 Apr 2026
Brief summary (registry, in English)
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.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 267 (actual)
- First submitted
- 16 Sept 2025
- Start date
- 2 Dec 2025
- Primary completion date
- Jan 2027
- Lead sponsor
- Hanmi Pharmaceutical Company Limited
- Diseases
- Obesity
- NCT number
- NCT07205900
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 267
- From 2 Dec 2025 to the primary completion date, Jan 2027
- 14 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Planned or prior obesity surgery (unless \>1 year ago for liposuction/abdominoplasty), or device-based obesity therapy (unless removed \>6 months ago)
- Have taken weight loss drugs, including over-the-counter medications, within 90 days prior to screening.
- History or current diagnosis of congestive heart failure (NYHA class Ⅲ or Ⅳ), or myocardial infarction, stroke, unstable angina, transient ischemic attack, or revascularization procedure (e.g., stent or bypass graft surgery) within 3 months prior to screening visit
Other illness
- Obesity due to endocrine/genetic disorders
- Personal history or current diagnosis of acute or chronic pancreatitis or factors that may increase the risk of pancreatitis, such as a history of cholelithiasis (without cholecystectomy) or alcohol abuse.
- Personal or family history of medullary thyroid carcinoma (MTC) or a known genetic condition (e.g., multiple endocrine neoplasia type 2) that predisposes the participant to MTC.
- Personal history or current diagnosis of acute or chronic pancreatitis or factors that may increase the risk of pancreatitis, such as a history of cholelithiasis (without cholecystectomy) or alcohol abuse.
Lab values
- Type 1 diabetes mellitus or T2DM, or HbA1c ≥6.5% / FPG ≥126 mg/dL
Who the study is looking for
- Participant's age at the time of signing the informed consent:
- United States: 18 to 75 years (inclusive)
- Korea: 19 to 75 years (inclusive)
- BMI ≥30 kg/m² and ≤50 kg/m², or ≥27 kg/m² and \<30 kg/m² with ≥1 weight-related comorbidity
- Body weight change \<5% over the past 3 months prior to screening
- Capable of giving signed informed consent, ability and willingness to comply with all protocol procedures
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (14)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Accellacare of McFarland Coordinator of this site? Confirm its status | Ames | United States | Unknown status |
| Texas Clinical Research Institute Coordinator of this site? Confirm its status | Arlington | United States | Unknown status |
| Bristol-Internal Medicine and Pediatric Associates of Bristol, P.C. Coordinator of this site? Confirm its status | Bristol | United States | Unknown status |
| Accellacare of Bristol-PAC of Tennessee Coordinator of this site? Confirm its status | Bristol | United States | Unknown status |
| Accellacare of Cary - Cary Medical Group Coordinator of this site? Confirm its status | Cary | United States | Unknown status |
| ProSciento, Inc. Coordinator of this site? Confirm its status | Chula Vista | United States | Unknown status |
| Velocity Clinical Research, Dallas Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| Accellacare of Hickory Coordinator of this site? Confirm its status | Hickory | United States | Unknown status |
| Accellacare of Charleston Coordinator of this site? Confirm its status | Mt. Pleasant | United States | Unknown status |
| Accellacare of Duly - Duly Oak Lawn Coordinator of this site? Confirm its status | Oak Lawn | United States | Unknown status |
| Raleigh Medical Group, P.A. Coordinator of this site? Confirm its status | Raleigh | United States | Unknown status |
| Accellacare of Piedmont - Piedmont HealthCare Coordinator of this site? Confirm its status | Statesville | United States | Unknown status |
| Accellacare of Wilmington, LLC Coordinator of this site? Confirm its status | Wilmington | United States | Unknown status |
| Accellacare of Winston Salem Coordinator of this site? Confirm its status | Winston-Salem | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.