drugset / Trial / NCT03725033

Clinical Trial of Efficacy and Safety of Subetta in the Treatment of Impaired Glucose Tolerance

NCT03725033 ↗

Phase 3 Completed 538 enrolled Materia Medica Holding
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Purpose of the study: * to assess the efficacy of Subetta in the treatment of impaired glucose tolerance * to assess the safety of Subetta in the treatment of impaired glucose tolerance.

Timeline

Start
2018-10-10
Primary completion
2020-03-23
Completion
2020-03-23

Outcome

Met primary endpoint

registry analysis (superiority test); Subetta vs Placebo; p = 0.0028; Wilcoxon (Mann-Whitney) NCT03725033 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Subetta Protein / enzyme biologic — Oral

Indications