Phase 3 Clinical Trial of Buagafuran Capsules in the Treatment of GAD

Status Recruiting

Clinical Trial Summary

A placebo-controlled superiority design was used to evaluate the efficacy of 60 mg/ day or 120 mg/ day of Buagafuran capsules in the treatment of GAD

Clinical Trial Description

This was a multi-center, randomized, double-blind, placebo-controlled, fixed-dose phase III clinical trial. Hierarchical factors for whether new generalized anxiety disorder (GAD) (new GAD vs. Non-new GAD). Qualified subjects, according to the ratio of 1:1:1, were randomized into high-dose group, low-dose group and placebo-control group, and received a treatment course of 8 weeks. Participants were followed from baseline outpatient visit until end of the follow-up period( 10 weeks and 7 visits in total). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06243640
Study type	Interventional
Source	Beijing Union Pharmaceutical Factory Ltd
Contact	Tao Sun
Phone	13621169498
Email	sunny.suntao@aliyun.com
Status	Recruiting
Phase	Phase 3
Start date	July 25, 2023
Completion date	June 30, 2027

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Phase 3 Clinical Trial of Buagafuran Capsules in the Treatment of GAD — BGFN-2022-02

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms