drugset / Trial / NCT05586789

A Study of the Efficacy and Safety of Ranquilon Tablets in Patients With Anxiety in Neurasthenia and Adjustment Disorders

NCT05586789 ↗

Phase 3 Completed 220 enrolled Valenta Pharm JSC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of the study is to evaluate the efficacy of Ranquilon, 1 mg tablets, at a dose of 6 mg/day compared to placebo for the treatment of patients with anxiety in neurasthenia and adjustment disorder. An additional study objective was to evaluate the safety of Ranquilon, 1 mg tablets, at a dose of 6 mg/day compared to placebo in patients with anxiety in neurasthenia and adjustment disorder.

Timeline

Start
2022-10-12
Primary completion
2022-11-22
Completion
2023-01-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Ranquilon Unknown 6 mg —