Orforglipron
DrugAdministered orally once daily
Other names: LY3502970
NCT Number: NCT05803421
The main purpose of this study is to determine safety and efficacy of orforglipron compared with insulin glargine in participants with type 2 diabetes and obesity or overweight at increased cardiovascular risk. The study will last approximately 2 years may include up to 27 visits.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Buenos Aires Macula S.A, Buenos Aires, Argentina
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Administered orally once daily
Other names: LY3502970
Administered SC once daily
Time frame: Baseline to End of the Study (Approximate Maximum 104 Weeks)
Time to First Occurrence of Any MACE-4 (Myocardial Infarction (MI), Stroke, Hospitalization for Unstable Angina, or Cardiovascular [CV] Death)
Time frame: Baseline to End of the Study (Approximately 104 Weeks)
Time to First Occurrence of Any MACE-3 Event (MI, Stroke, or CV death)
Time frame: Baseline, Week 52
Change from Baseline in HbA1c
Time frame: Baseline, Week 52
Change from Baseline in Fasting Serum Glucose
Time frame: Baseline, Week 52
Change from Baseline in Daily Average 7-point SMBG
Time frame: Week 52
Percentage of Participants with HbA1c Target Values <7.0% (53 mmol/mol)
Time frame: Baseline, Week 52
Change from Baseline in Body Weight
Time frame: Week 52
Percent Change from Baseline Body Weight
Time frame: Baseline, Week 52
The SF-36v2 acute form is a 36-item generic, participant completed measure designed to assess 8 domains: physical functioning, role-physical, bodily pain, general health, vitality, social functioning, role-emotional, and mental health. Scores of each domain are measured by T-scores, with a mean of 50 and standard deviation of 10; higher scores indicate better levels of function and/or better health.
Time frame: Baseline through Week 52
PK will be estimated based on the population PK model.
Eli Lilly and Company
Industry
A Phase 3, Open-Label Study of Once Daily LY3502970 Compared With Insulin Glargine in Adult Participants With Type 2 Diabetes and Obesity or Overweight at Increased Cardiovascular Risk
Acronym: ACHIEVE-4
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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