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A Randomized, Double-blind, Placebo-controlled, Dose-escalation Phase I Study on the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SHR-2906 Injection in Healthy Subjects With a Single Dose and in Obese Patients With Multiple Doses

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

This study is a randomized, double-blind, placebo-controlled, dose-escalation phase I clinical trial. This study consists of two parts: the single-dose escalation study (SAD) in healthy subjects and the multiple-dose escalation study (MAD) in obese patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 55
Healthy Volunteers: t
View:

• Voluntarily sign the informed consent form prior to any study-related activities, understand the procedures and methods of the study, and agree to complete this study in strict accordance with the clinical study protocol;

• Males or females aged 18-55 years (inclusive);

• Subjects who are generally healthy as judged by the investigator based on medical history, vital signs, physical examination, laboratory tests, and electrocardiogram (ECG);

• At screening, 19.0 ≤ BMI ≤ 23.9 kg/m2 (inclusive) for Part I or 28.0 ≤ BMI ≤ 35.0 kg/m2 (inclusive) for Part II.

Locations
Other Locations
China
Hangzhou First People's Hospital
RECRUITING
Hangzhou
Contact Information
Primary
Zi Ye
zi.ye@hengrui.com
+86-0518-81220121
Time Frame
Start Date: 2026-01-05
Estimated Completion Date: 2026-12
Participants
Target number of participants: 124
Treatments
Experimental: SHR-2906 Injection Group
Placebo_comparator: SHR-2906 Injection Placebo Group
Related Therapeutic Areas
Sponsors
Leads: Beijing Suncadia Pharmaceuticals Co., Ltd

This content was sourced from clinicaltrials.gov

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