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NCT06174779CompletedPhase 3

A Study to Evaluate Efficacy and Safety of HM11260C in Adult Obesity Patients Without Diabetes Mellitus

A Multicenter, Randomized, Double-blind, Phase 3 Study to Evaluate Efficacy and Safety of HM11260C in Adult Obesity Patients Without Diabetes Mellitus

Source: ClinicalTrials.gov · Last updated 7 Jul 2026

Brief summary (registry, in English)

A multicenter, randomized, double-blind, phase 3 study to evaluate efficacy and safety of HM11260C in adult obesity patients without diabetes mellitus

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
448 (actual)
First submitted
8 Dec 2023
Start date
3 Jan 2024
Primary completion date
14 Aug 2025
Lead sponsor
Hanmi Pharmaceutical Company Limited
Diseases
Obesity
NCT number
NCT06174779

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 448
  • From 3 Jan 2024 to the primary completion date, 14 Aug 2025
  • 1 site 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

  • A person whose weight change exceeds 5kg within 3 months prior to screening visit.
  • Administration of Steroids for the systemic use.
  • Hypersensitivity to investigational products or multi-drug allergy.

Other illness

  • Prader-Willi Syndrome or MC4R deficiency.
  • Cushing's Syndrome.
  • A person who has a history of surgery(including device-based therapy) related to obesity or who has a plan during the clinical trial period.
  • History of acute or chronic pancreatitis.
  • Answered 'yes' to question 4 or 5 of the suicidal ideation domain in C-SSRS or history of suicide attempt.
  • PHQ-9 ≥ 15 or history of depression, anxiety, and other severe Mental illness.
  • History of alcohol addiction or drug abuse.
  • History of malignant tumors.
  • History of severe heart disease or severe neurovascular disease.

Lab values

  • Diabetes mellitus (Type 1, type 2, etc.) or HbA1c ≥ 6.5 %.
  • A person who has the following clinical laboratory test results :
    • TSH \< 0.4 mIU/L or TSH \> 6 mIU/L
    • Calcitonin \> 100 ng/L
    • Amylase or Lipase \> 3 x UNL
  • Severe liver disease (AST or AST \> 3 x UNL or Total bilirubin \> 1.5 x UNL).
  • Severe renal disease ( eGFR \< 30mL/min/1.73m 2 ).
  • QTc \> 450 ms.

Other

  • Administration of hypoglycemic agents.
  • Administration of medicines inducing weight gain.
  • Administration of medicines for weight management.
  • Clinically significant gastric emptying abnormalities.
  • History(including family history) of medullary thyroid carcinoma or multiple endocrine adenomatosis.
  • Positive to pregnancy test, nursing mother, intention on pregnancy.
  • Considered by investigator as not appropriate to participate in the clinical study with other reason.

Who the study is looking for

  • Patients with following criteria :
    • BMI ≥ 30 kg/m2 or
    • 27 kg/m2 ≤ BMI \< 30 kg/m2 with more than one risk factors or comorbidities(hypertension, dyslipidemia, sleep apnea, cardiocerebrovascular disease)
  • A person who have failed at least once to weight control using diet and exercise therapy before screening visit.

Age in the registry: 19 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Kangbuk Samsung Hospital
Coordinator of this site? Confirm its status
SeoulSouth KoreaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.