drugset / Trial / NCT01986881

Cardiovascular Outcomes Following Ertugliflozin Treatment in Type 2 Diabetes Mellitus Participants With Vascular Disease, The VERTIS CV Study (MK-8835-004)

NCT01986881 ↗

Phase 3 Completed 8246 enrolled Merck Sharp & Dohme LLC Pfizer · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

An overall study of the cardiovascular outcomes following treatment with ertugliflozin in participants with type 2 diabetes mellitus (T2DM) and established vascular disease. The main objective of this study is to assess the cardiovascular safety of ertugliflozin. This trial includes 3 pre-defined glycemic sub-studies; 1. In participants receiving background insulin with or without metformin, 2. In participants receiving background sulfonylurea monotherapy, and 3. In participants receiving background metformin with sulfonylurea (all fully-enrolled). Participants enrolled prior to Amendment 1 were in the overall study as well as a sub-study, if they met certain entry criteria. Participants enrolled following the start of Amendment 1 were only enrolled in the overall study. The sub-studies were the initial 18 weeks of the overall study period.

Timeline

Start
2013-11-04
Primary completion
2019-12-27
Completion
2019-12-27

Outcome

Sources disagree · no verdict is set; each source's reading is shown below

paper Among patients with type 2 diabetes and atherosclerotic cardiovascular disease, ertugliflozin was noninferior to placebo with respect to major adverse cardiovascular events. reads as mixed primary results PMID 32966714 ↗

registry Ertugliflozin 15 mg (Insulin +/- Metformin Glycemic Sub-study) vs Placebo (Ins+/-Met Sub-study); p <0.001; Difference in the Least Squares Means -0.65 reads as mixed primary results NCT01986881 ↗

registry Ertugliflozin 15 mg (Sulfonylurea Monotherapy Glycemic Sub-study) vs Placebo (Sulfonylurea Monotherapy Glycemic Sub-study); p = 0.247 reads as mixed primary results NCT01986881 ↗

registry Ertugliflozin 5 mg (Sulfonylurea Monotherapy Glycemic Sub-study) vs Placebo (Sulfonylurea Monotherapy Glycemic Sub-study); p = 0.063 reads as mixed primary results NCT01986881 ↗

registry Ertugliflozin 15 mg (Metformin With Sulfonylurea Glycemic Sub-study) vs Placebo (Metformin With Sulfonylurea Glycemic Sub-study); p <0.001 reads as mixed primary results NCT01986881 ↗

release “Phase 3 VERTIS CV cardiovascular (CV) outcomes trial for STEGLATRO (ertugliflozin), an oral sodium-glucose cotransporter 2 (SGLT2) inhibitor, achieved its primary endpoint of non-inferiority” reads as met primary endpoint merck.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ertugliflozin Unknown 5 mg Oral
Subject Ertugliflozin Unknown 15 mg Oral