Oral drug for obesity tested in First-in-Human trial
NCT ID NCT07815678
First seen Sep 11, 2026 · Last updated Sep 15, 2026 · Updated 2 times
Summary
Researchers are testing a new oral drug called ACCG-2671 to see if it is safe and how the body processes it. The trial includes healthy volunteers and people with obesity, some of whom are already taking a GLP-1 drug for weight loss. Participants will receive either ACCG-2671 or a placebo to compare effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- an experimental oral drug called ACCG-2671
- What this could lead to
- If it works, this could lead to a new oral treatment for obesity, offering an alternative to injections.
- What could go wrong
- This is an early-stage trial with a small number of participants. Many drugs fail in early testing due to side effects or poor performance, so it may not advance.
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 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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About 164 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2025
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- 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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25 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Signed informed consent * Men and women with the following at the time of Screening for Part 1 and 2: ≥25 years and ≤65 years of age and BMI ≥18.0 kg/m2 and \<30.0 kg/m2 * For Part 3, ≥25 years and ≤75 years of age and BMI ≥30.0 kg/m2 * For Part 3, receiving a stable dose of an injectable GLP-1RA for ≥3 months, who responded to GLP1RA treatment with stable body weight and no ongoing GLP-1RA-related symptoms or AEs. For the duration of the study, participants must not be planning to change GLP-1RA dose or discontinue GLP-1RA treatment * Body weight ≥50.0 kg at time of screening Exclusion Criteria: * For Parts 1 and Part 2: Participants with any clinically significant medical conditions are excluded from the study. * For Parts 1, 2 and 3: participants will be excluded from this study if there is evidence of ANY of the exclusion criteria at the Screening Visit or prior to first dose administration * History or presence of significant CV, pulmonary, hepatic, renal, hematological, GI, endocrine, immunologic, dermatologic, psychiatric, or neurological disease, including any acute illness or major surgery within the past 3 months, or any clinical laboratory abnormality determined by the Investigator to be clinically significant * Use of any prescription or over-the counter-medication including herbal products, diet aids, vitamins, or hormone supplements (including contraceptives) within 10 days or 5 times the apparent elimination half-life of the medication (whichever is longer) before the first study drug administration and throughout the study. Exceptions include injectable GLP-1RA treatment for Part 3, Cohort 2c only and medications used to manage AEs at the discretion of an investigator after consultation with the Sponsor.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
6 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Show contact details
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Locations
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Research Site
NOT_YET_RECRUITINGCypress, California, 90630, United States
Contact Email: •••••@•••••
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Research Site
RECRUITINGLake Forest, California, 92630, United States
Contact Email: •••••@•••••
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Research Site
NOT_YET_RECRUITINGDecatur, Georgia, 30030, United States
Contact Email: •••••@•••••
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Research Site
RECRUITINGDilworth, Minnesota, 56529, United States
Contact Email: •••••@•••••
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Research Site
NOT_YET_RECRUITINGSpringfield, Missouri, 65802, United States
Contact Email: •••••@•••••
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Research Site
RECRUITINGWebster, Texas, 77598, United States
Contact Email: •••••@•••••
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