Primary Objective: To demonstrate that efpeglenatide 4 and 6 mg was noninferior to placebo on 3-point major adverse cardiac events (MACE) in Type 2 diabetes mellitus (T2DM) participants at high cardiovascular (CV) risk. Secondary Objectives: To demonstrate that efpeglenatide 4 and 6 mg was superior to placebo in T2DM participants with high CV risk on the following parameters: * 3-point MACE. * Expanded CV outcome. * Composite outcome of new or worsening nephropathy. To assess the safety and tolerability of efpeglenatide 4 and 6 mg, both added to standard of care in T2DM participants at high CV risk.
The study duration per participant was up to approximately 36 months.
Pharmaceutical form: Solution for injection, Route of administration: SC
Pharmaceutical form: Solution for injection Route of administration: SC
Buenos Aires, Argentina
Caba, Argentina
Caba, Argentina
Caba, Argentina
Caba, Argentina
Capital Federal, Argentina
Capital Federal, Argentina
Corrientes, Argentina
Corrientes, Argentina
Godoy Cruz, Argentina
Mar del Plata, Argentina
Merlo, Argentina
Rosario, Argentina
Rosario, Argentina
Salta, Argentina
Salta, Argentina
San Isidro, Argentina
Santa Rosa, Argentina