New weight loss drug shows promise in Long-Term Follow-Up study
NCT ID NCT06671821
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at the long-term safety and effectiveness of the drug HRS-7535 for weight management in 81 adults with obesity who had already completed a 36-week treatment course. Participants took the drug for an additional 32 weeks to see how well it helped maintain weight loss and whether any side effects appeared. The goal is to see if HRS-7535 can be a safe and effective long-term option for managing obesity.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- HRS-7535 (a drug tablet for weight loss)
- What this could lead to
- If successful, this could support HRS-7535 as a long-term weight management option for obesity, potentially helping people achieve and maintain significant weight loss.
- What could go wrong
- This is a small, completed Phase 2 extension study with only 81 participants. Long-term safety and efficacy are still being evaluated, and results may not apply to all people with obesity.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
81 people
The number who actually took part.
- Started
-
Nov 2024
- Finished
-
Sep 2025
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male or female subjects, 18-65 years of age at the time of signing informed consent; 2. Subjects who have completed the entire 36-week treatment course of the HRS-7535-202 trial. 3. Subjects who have a full understanding of the trial content, processes, and possible adverse reactions, and are capable and willing to comply with the protocol requirements to complete this study. Exclusion Criteria: 1. Participants with poor compliance during the 36-week open-label extension treatment of the HRS-7535-202 trial; 2. Pregnant, lactating, planning to conceive during the trial period, or fertile subjects unwilling to take effective contraceptive measures during the trial period. 3. Any other conditions deemed unsuitable for participation in this clinical trial by the investigator.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Chinese PLA General Hospital
Beijing, Beijing Municipality, 100039, China
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