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

Trial statusNot yet recruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-65
SponsorShanghai JMT-Bio Inc.

About this trial

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Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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..

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • JMT206 injection

    Drug

    JMT206 injection administered subcutaneously (SC) once a week

  • Semaglutide injection

    Combination product

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

  • Placebo injection

    Drug

    Placebo administered subcutaneously (SC) once a week.

Treatment groups

90 Participants
are divided into 8 treatment groups

8

Treatment groups

See each treatment group below.

Group A: JMT206 injection group 2Experimental treatment 1 intervention
Group B: JMT206 injection group 3Experimental treatment 1 intervention
Group C: JMT206 injection + Semaglutide group 1Experimental treatment 2 interventions
Group D: JMT206 injection + Semaglutide group 2Experimental treatment 2 interventions
Group E: JMT206 injection + Semaglutide group 3Experimental treatment 2 interventions
Group F: PlaceboPlacebo comparator 1 intervention
Group G: Placebo+ SemaglutidePlacebo comparator 2 interventions
Group H: JMT206 injection group 1Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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

Time frame
Baseline through week 19

Secondary outcomes

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: