New diabetes pill shows promise for patients stuck on ozempic
NCT ID NCT07502508
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new daily pill, icovamenib, for people with type 2 diabetes who still have high blood sugar despite taking Ozempic. About 60 adults will receive either the pill or a placebo for 12 weeks. The main goal is to see if the pill lowers HbA1c (a measure of blood sugar control) better than a placebo.
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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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Jul 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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18 to 70 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. Males or females, age ≥18 years and ≤70 years 2. Have been diagnosed with T2D 3. Taking Ozempic (semaglutide injection) and have been treated with lifestyle management and 0 to 2 additional antihyperglycemic medications (metformin and/or SGLT2 inhibitor) with a stable dose of all medications for at least 3 months prior to screening * If participants are taking metformin, they must be on a minimum stable dose of ≥500 mg/day * Participants must be on a minimum stable dose of Ozempic ≥0.5 mg/week 4. Have HbA1c ≥7.5 and ≤9.5% 5. Have a BMI 25 to 40 kg/m2 6. Female participants of childbearing potential must have a negative pregnancy test, must be non-lactating, must be willing to have additional pregnancy tests during the study, must agree to the sex and contraception requirements. 7. Willing and able to provide written, signed informed consent and be willing and able to comply with all study procedures and tests. Key Exclusion Criteria: 1. Have type 1 diabetes mellitus or a secondary form of diabetes 2. Have a history of diabetic ketoacidosis or hyperosmolar coma in the 6 months prior to screening 3. Have a history of severe hypoglycemia (defined by the occurrence of hypoglycemia symptoms requiring the assistance of another person for recovery) in the 6 months prior to screening or a history of hypoglycemia unawareness or poor recognition of hypoglycemic symptoms as judged by the investigator 4. Have personal or family history (first-degree relative) of MEN1 or MEN2 or medullary thyroid carcinoma 5. Use of GLP-1 RA other than Ozempic (semaglutide injection), dual GIP/GLP-1 RA, sulfonylureas, meglitinides, thiazolidinediones, alpha glucosidase inhibitor, DPP4I, bile acid sequestrants, dopamaine-2 agonists, amylin, or insulin in the 3 months prior to screening 6. Have FPG ≥240 mg/dL
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Genom att skicka in godkänner du våra Användarvillkor
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
17 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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Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
Locations
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Ark Clinical Research
RECRUITINGLong Beach, California, 90815, United States
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Burke Internal Medicine and Research
RECRUITINGBurke, Virginia, 22015, United States
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Catalina Research Institute, LLC
RECRUITINGMontclair, California, 91763, United States
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Central Research Associates, LLC dba Flourish Research
RECRUITINGBirmingham, Alabama, 35205, United States
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David Kavtaradze MD, Inc
RECRUITINGCordele, Georgia, 31015, United States
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Diabetes & Glandular Disease Clinic, P.A.
RECRUITINGSan Antonio, Texas, 78229, United States
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Diabetes and Endocrinology Associates of Stark County
RECRUITINGCanton, Ohio, 44718, United States
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Elligo Health Research, Inc.
RECRUITINGAustin, Texas, 78704, United States
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Epic Clinical Research
RECRUITINGLewisville, Texas, 75057, United States
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Excel Clinical Research
RECRUITINGLas Vegas, Nevada, 89109, United States
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Flourish Research Orlando
RECRUITINGWinter Park, Florida, 32789, United States
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Hope Clinical Research
RECRUITINGCanoga Park, California, 91303, United States
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Panax Clinical Research
RECRUITINGMiami Lakes, Florida, 33014, United States
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Paradigm Clinical Research Centers, LLC
RECRUITINGSan Diego, California, 92108, United States
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Southwest General Healthcare Center
RECRUITINGFort Myers, Florida, 33907, United States
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Synergy Group Medical
RECRUITINGHouston, Texas, 77061, United States
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Zenos Clinical Research
RECRUITINGDallas, Texas, 75230, United States
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