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NCT07840729RecruitingPhase 1

Evaluate the Safety and Tolerability of Multiple Doses of JMT206 Injection in Obese Participants

Identify the Expanded Access Program, if Any. This is Required Unless the Expanded Access Type is "Individual Patients." A Randomized, Parallel, Double-blind, Placebo-controlled Phase I Clinical Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of JMT206 Injection Alone or in Combination With Semaglutide in Obese Participants

Source: ClinicalTrials.gov · Last updated 2 Nov 2026

Brief summary (registry, in English)

Use these resources to provide understandable information about this study to patients, families, and health care providers:

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
90 (estimated)
First submitted
20 Sept 2026
Start date
20 Oct 2026
Primary completion date
28 Feb 2027
Lead sponsor
Shanghai JMT-Bio Inc.
Diseases
Obesity
NCT number
NCT07840729

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 90
  • From 20 Oct 2026 to the primary completion date, 28 Feb 2027
  • 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

  • 1\) Those known to have a history of allergy to any component or related preparations in the investigational drug and its excipients, or have severe allergic diseases or allergic constitution; 2) Participants with a history of diabetes mellitus or hypoglycemic episodes; 3) Obesity is related to medication or diseases; Or weight gain caused by non-fat content; or monogene mutationsobesity; 4) History of weight loss surgery and/or treatment within the past year; 5) History of severe gastrointestinal disease or gastrointestinal surgery, clinically significant gastric emptying abnormalities, or long-term use of medications directly affecting gastrointestinal motility; 6) Having comorbidities known to affect skeletal muscle proteins; 7) A history of acute or chronic pancreatitis; 8) Acute gallbladder disease within one year prior to screening; 9) Previous or family history of medullary thyroid carcinoma or type 2 endocrine adenomatosis; 10) Severe cardiovascular or cerebrovascular events within 6 months prior to screening; 11) Any type of treated or untreated malignant tumor within 5 years prior to screening; 12) History of severe mental illness; 13) Use of drugs or products that may cause weight changes within 3 months prior to screening; 14) Use of drugs or products affecting skeletal muscle synthesis within 3 months prior to screening; 15) Participants deemed otherwise unsuitable for this trial by the investigator.

Other

  • \-

Who the study is looking for

  • Age 18\~65 (including threshold values), male or female participants;
  • BMI ≥ 30 kg/m²;
  • Weight change \<5% within the 3 months prior to screening
  • Voluntarily sign the informed consent form before the trial..

Age in the registry: 18 years to 65 years · 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
Peking University People's Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

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