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New weight loss pill shows promise in early trial
NCT ID NCT06854952
First seen Jun 27, 2026 · Last updated Aug 11, 2026 · Updated 2 times
Summary
This study tested an experimental oral medication called TERN-601 in 167 adults with overweight or obesity. The goal was to see if it helps with weight loss over 12 weeks compared to a placebo. Participants did not have diabetes and had a stable weight before starting. The study is complete, and results will show how much weight was lost and if the drug is safe.
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
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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167 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Sep 2025
- Lead sponsor
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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
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18 to 75 years
- Sex
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Anyone
- Healthy volunteers
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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.
Key Inclusion Criteria: 1. Female or male aged 18 to 75 years 2. Body mass index (BMI) of: 1. ≥ 30 kg/m\^2 to \< 50 kg/m\^2 OR 2. ≥ 27 kg/m\^2 to \< 30 kg/m\^2 with at least 1 weight-related comorbidity 3. HbA1c \< 6.5% 4. Stable self-reported body weight for at least 3 months prior to study (\< 5% body weight gain or loss) Key Exclusion Criteria: 1. Have diabetes mellitus 2. Have obesity induced by medication or other diagnosed endocrinologic disorders 3. Have had or are planning surgical treatment or device-based therapy for obesity 4. Lifetime history of suicide attempt
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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
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FALCON Research Site
Birmingham, Alabama, 35294, United States
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FALCON Research Site
Homewood, Alabama, 35209, United States
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FALCON Research Site
Tucson, Arizona, 85712, United States
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FALCON Research Site
Spring Valley, California, 91978, United States
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FALCON Research Site
Port Orange, Florida, 32127, United States
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FALCON Research Site
Louisville, Kentucky, 40213, United States
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FALCON Research Site
Marrero, Louisiana, 70072, United States
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FALCON Research Site
Boston, Massachusetts, 02114, United States
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FALCON Research Site
Rochester, Minnesota, 55905, United States
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FALCON Research Site
City of Saint Peters, Missouri, 63303, United States
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FALCON Research Site
Beachwood, Ohio, 44122, United States
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FALCON Research Site
Medford, Oregon, 97504, United States
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FALCON Research Site
Dallas, Texas, 75230, United States
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FALCON Research Site
Houston, Texas, 77079, United States
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FALCON Research Site
San Antonio, Texas, 78229, United States
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FALCON Research Site
St. George, Utah, 84790, United States
-
FALCON Research Site
Arlington, Virginia, 22206, United States
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Other studies related to the condition(s) this trial covers.
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