Type 2 diabetes affects roughly 37 million Americans and happens when the body can't use insulin properly. Treatment has evolved from lifestyle changes and metformin to include GLP-1 receptor agonists like semaglutide, SGLT2 inhibitors, and insulin when needed. Many people now achieve blood sugar control that reduces heart and kidney complications.
What's actually going on in research
Trials are testing dual and triple hormone agonists that may improve weight and blood sugar beyond current drugs, earlier use of combination therapies, medications that protect the heart and kidneys independent of blood sugar control, and approaches to preserve the insulin-producing beta cells. Researchers are also studying whether treating diabetes differently based on individual disease mechanisms improves outcomes.
Dual and triple agonists
Drugs that activate GLP-1 plus GIP or glucagon receptors are showing greater weight loss and blood sugar improvement than single-hormone drugs. Tirzepatide received FDA approval in 2022, and other combinations are in testing.
Cardiovascular protection
Newer diabetes drugs protect the heart and kidneys beyond their effects on blood sugar. Trials are testing whether starting these medications earlier prevents complications even in people with well-controlled diabetes.
Beta cell preservation
Studies are testing drugs that might protect or restore the insulin-producing cells that decline in type 2 diabetes. If successful, they could change the disease course rather than just managing symptoms.
What to know before you search
Eligibility typically depends on hemoglobin A1c level, years since diagnosis, current medications, weight, and presence of complications like heart or kidney disease.
What types of trials are currently open
- Treatment trials — Testing new diabetes medications or combinations to see if they lower blood sugar, promote weight loss, or work better than current options.
- Cardiovascular outcome trials — Large studies following people for years to see if a diabetes drug prevents heart attacks, strokes, and death. Required by FDA for most new diabetes medications.
- Kidney protection trials — Testing whether diabetes medications slow kidney disease progression or prevent kidney failure.
- Prevention trials — Studies in people with prediabetes testing whether medications, lifestyle programs, or both can prevent or delay type 2 diabetes.
- Device trials — Testing continuous glucose monitors, insulin pumps, and automated insulin delivery systems in people with type 2 diabetes who use insulin.
Recently added Type 2 Diabetes trials
Take weekly injections of a new diabetes and weight loss medication
This trial is conducted in China. The aim is to compare BGM0504 Injection 15 mg with semaglutide 1.0 mg in Chinese T2DM patients with obesity and inadequate control despite diet and exercise. Over 52 weeks of once weekly treatment, efficacy and safety are evaluated, including the rate of diabetes remission at 12 weeks after treatment discontinuation.
Try a personalized lifestyle program to improve your heart and metabolic health
The goal of this clinical trial is to evaluate whether a precision lifestyle medicine intervention can improve cardiometabolic health in Emirati adults aged 25 to 50 years living in Abu Dhabi with obesity (BMI 30-35 kg/m²) who have previously completed IFHAS screening. The study will also use IFHAS screening data to better understand participants' health profiles and the relationship between lifestyle factors and chronic diseases. The main questions it aims to answer are: * Does a precision lifestyle medicine program improve cardiometabolic biomarkers after an 18-week intervention? * Can IFHAS screening data be used to identify health risk profiles and support personalized lifestyle interventions for the Emirati population? Researchers will compare participants receiving the precision lifestyle medicine intervention with a propensity-matched control group receiving standard IFHAS care to determine whether the intervention leads to greater improvements in cardiometabolic health. Participants will: * Take part in an 18-week personalized lifestyle medicine program tailored to their health profile. * Attend study visits and complete health assessments over a total study period of 24 weeks. * Undergo cardiometabolic biomarker assessments before and after the intervention. * Complete questionnaires or assessments about their adherence to the lifestyle program and their experience with the precision lifestyle medicine clinic. * Provide biological samples to support the establishment of a biomarker repository for future research.
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