Condition: Type 2 Diabetes · Sponsor: Biomea Fusion Inc.
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Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.
This is a Phase 2, randomized, double-blind, placebo-controlled trial assessing the efficacy and safety of icovamenib in participants with Type 2 Diabetes who are not achieving glycemic targets despite antihyperglycemic medications.
This description comes directly from the study's public registry record.
Biomea Fusion Inc. · 1-844-245-0490 · clinicaltrials@biomeafusion.com
There is no obligation to join — the study team can answer your questions about taking part.
Always discuss trial participation with your own doctor first.
Key Inclusion Criteria: 1. Males or females, age ≥18 years and ≤75 years 2. Diagnosed with T2D 3. Have been treated with lifestyle management with 1 to 3 antihyperglycemic medications: metformin, SGLT2i, alogliptin, or sitagliptin with a stable dose 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) 4. Have HbA1c ≥7.5 and ≤10.5% 5. Have a BMI ≤32 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, and 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 positive GAD autoantibody result within 60 days prior to screening 4. 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 5. Have personal or family history (first-degree relative) of MEN1 6. Use of GLP-1 RA, dual GIP/GLP-1 RA, sulfonylureas, meglitinides, thiazolidinediones, alpha glucosidase inhibitor, \[linagliptin, saxagliptin (these 2 are drugs within DPP-4i class)\], bile acid sequestrants, dopamaine-2 agonists, amylin, or insulin in the 3 months prior to screening 7. Have fasting triglyceride ≥500 mg/dL 8. Have an eGFR \<60 mL/min/1.73 m2 by the CKD-EPI Creatinine Equation at screening 9. Have impaired liver function, defined as screening AST or ALT \>1.2×ULN, and/or total bilirubin \>ULN
Reproduced word-for-word from the public registry record — the study team can answer questions about it.
| Central Research Associates, LLC dba Flourish Research | Birmingham, Alabama, United States | Recruiting |
| Hope Clinical Research | Canoga Park, California, United States | Recruiting |
| Ark Clinical Research | Fountain Valley, California, United States | Recruiting |
| Ark Clinical Research | Long Beach, California, United States | Recruiting |
| Catalina Research Institute, LLC | Montclair, California, United States | Recruiting |
| Paradigm Clinical Research Centers, LLC | San Diego, California, United States | Recruiting |
| Southwest General Healthcare Center | Fort Myers, Florida, United States | Recruiting |
| Panax Clinical Research | Miami Lakes, Florida, United States | Recruiting |
| Clinical Site Partners, LLC dba Flourish Research | Winter Park, Florida, United States | Recruiting |
| David Kavtaradze MD, Inc | Cordele, Georgia, United States | Recruiting |
| Excel Clinical Research | Las Vegas, Nevada, United States | Recruiting |
| Diabetes and Endocrinology Associates of Stark County | Canton, Ohio, United States | Recruiting |
+ 6 more locations — full list on the registry record.
This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.
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