Elecoglipron for Type 2 Diabetes Management
A Phase III Study to Investigate the Efficacy and Safety of Elecoglipron Compared With Placebo in Adults With Type 2 Diabetes Mellitus on Background Insulin
- Age
- 18 and older
- Sex
- Any
- Trial phase
- Phase 3
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 600 (estimated)
- Sponsor
- AstraZeneca · Industry
This trial is looking for adults with type 2 diabetes who are already taking insulin and other medications to lower blood sugar. Participants will compare a new treatment called elecoglipron with a placebo to see how effective and safe it is.
You may be able to join if
- I have been diagnosed with type 2 diabetes for at least 90 days.
- I am currently taking background insulin and other diabetes medications.
- My HbA1c value is between 7% and 10.5%.
- My body mass index (BMI) is at least 23.
- I have maintained a stable body weight for the last 90 days.
You may not be able to join if
- I have type 1 diabetes or another form of diabetes.
- I am receiving treatment for diabetic eye problems.
- I have had more than one severe low blood sugar episode in the last 180 days.
- I have significant issues with my upper GI tract.
- I have a history of pancreatitis.
- I have severe heart failure.
- I have a history of medullary thyroid cancer in myself or family.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your EligibilityThe purpose of this study is to evaluate the efficacy, safety, and tolerability of elecoglipron compared with placebo in adults with Type 2 Diabetes Mellitus (T2DM), treated with a background insulin and other background glucose-lowering medication(s)
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AstraZeneca Clinical Study Information Center
1-877-240-9479
information.center@astrazeneca.com
CONTACT