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Study identifier: NCT06145893 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study of Efficacy and Safety of Hemay005 Tablets in Patients With Behçet's Disease

Condition: Behçet's Disease  ·  Sponsor: Ganzhou Hemay Pharmaceutical Co., Ltd

PhasePhase 3
Planned participants162
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This is a phase 3, 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 40 weeks and a follow up phase for 4weeks.

This description comes directly from the study's public registry record.

Talk to the study team

Jinfeng Lin  ·  15790249669  ·  linjinfeng@hemay.com.cn

Always discuss trial participation with your own doctor first.

Locations (22)

Beijing Friendship hospital capital medical hospitalBeijing, Beijing Municipality, ChinaRecruiting
Peking university first hospitalBeijing, Beijing Municipality, ChinaRecruiting
Peking University People's HospitalBeijing, Beijing Municipality, ChinaRecruiting
Peking university third hospitalBeijing, Beijing Municipality, ChinaRecruiting
Xuanwu hospital capital medical universityBeijing, Beijing Municipality, ChinaRecruiting
The first affiliated hospital of Xiamen UniversityXiamen, Fujian, ChinaRecruiting
Guangdong second provincial central hospitalGuangzhou, Guangdong, ChinaRecruiting
Sun Yat-Sen memorial hospitalGuangzhou, Guangdong, ChinaRecruiting
The third affiliated hospital sun yat-sen universityGuangzhou, Guangdong, ChinaRecruiting
The university of Hong Kong-Shenzhen HospitalShenzhen, Guangdong, ChinaRecruiting
Affiliated hospital of Guilin Medical universityGuilin, Guangxi, ChinaRecruiting
The second hospital of Hebei medical universityShijiazhuang, Hebei, ChinaNot Yet Recruiting

+ 10 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06145893