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Not yet recruitingNCT07840729Updated Sep 25, 2026

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

A Phase 1 interventional study of JMT206 injection and Semaglutide injection in Valid MeSH Conditiongs, sponsored by Shanghai JMT-Bio Inc.. Not yet recruiting at 1 site in China. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2026-09-25.

Sponsored by Shanghai JMT-Bio Inc. · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

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

02

Conditions studied

  • Valid MeSH Conditiongs
03

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

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.

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04

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    JMT206 injection group 2

    JMT206 injection dose 2 administered subcutaneously (SC) once a week

    Drug: JMT206 injection

  • Experimental
    JMT206 injection group 3

    JMT206 injection dose 3 administered subcutaneously (SC) once a week

    Drug: JMT206 injection

  • Experimental
    JMT206 injection + Semaglutide group 1

    JMT206 injection dose 1 administered subcutaneously (SC) once a week. Semaglutide administered subcutaneously once a week, starts from lower dose and is gradually increased.

    Drug: JMT206 injection · Combination Product: Semaglutide injection

  • Experimental
    JMT206 injection + Semaglutide group 2

    JMT206 injection dose 2 administered subcutaneously (SC) once a week. Semaglutide administered subcutaneously once a week, starts from lower dose and is gradually increased.

    Drug: JMT206 injection · Combination Product: Semaglutide injection

  • Experimental
    JMT206 injection + Semaglutide group 3

    JMT206 injection dose 3 administered subcutaneously (SC) once a week. Semaglutide administered subcutaneously once a week, starts from lower dose and is gradually increased

    Drug: JMT206 injection · Combination Product: Semaglutide injection

  • Placebo comparator
    Placebo

    Placebo administered subcutaneously (SC) once a week

    Drug: Placebo injection

  • Placebo comparator
    Placebo+ Semaglutide

    Placebo administered subcutaneously (SC) once a week. Semaglutide administered subcutaneously once a week, starts from lower dose and is gradually increased.

    Combination Product: Semaglutide injection · Drug: Placebo injection

  • Experimental
    JMT206 injection group 1

    JMT206 injection dose 1 administered subcutaneously (SC) once a week

    Drug: JMT206 injection

Interventions

  • DrugJMT206 injection

    JMT206 injection administered subcutaneously (SC) once a week

  • Combination productSemaglutide injection

    Semaglutide administered subcutaneously once a week, starts from lower dose and is gradually increased.

  • DrugPlacebo injection

    Placebo administered subcutaneously (SC) once a week.

05

What researchers measure

Primary outcomes

  1. Incidence of Adverse Events (AE) assessed by CTCAE v6.0

    Time frame: Baseline through week 19

06

Study locations

1 site
  • Peking University People's Hospital
    Beijing, China
07

Registry details

Key details

Study ID
NCT07840729
Lead sponsor
Shanghai JMT-Bio Inc.
Responsible party
Sponsor
First posted
Sep 25, 2026
Start date
Oct 20, 2026 (estimated)
Primary completion
Feb 28, 2027 (estimated)
Completion
Apr 30, 2027 (estimated)
Last update
Sep 25, 2026

Study contacts

Clinical Trials Information Group officer
Contact
ctr-contact@mail.ecspc.com
86-0311-69085587

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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