Overview

A Study to Evaluate the Efficacy and Safety of Hemay005 in the Treatment of Behçet Disease

Status:
Recruiting
Trial end date:
2022-01-31
Target enrollment:
Participant gender:
Summary
This is a phase 2, multi-center, randomized, placebo-controlled, double-blind, parallel-group study with an equal randomization among the Hemay005 high dose, lower dose and placebo treatment groups. After subject randomization, each subject will enter an core-treatment Phase for 12 weeks following an extended-treatment phase for another 12weeks and a follow up phase for 4weeks.
Phase:
Phase 2
Details
Lead Sponsor:
Tianjin Hemay Pharmaceutical Co.,Ltd
Collaborator:
Shanghai Bestudy Medical Technology Co., Ltd
Treatments:
Hemay005