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Study identifier: NCT05837897 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study of Vedolizumab in Adult Participants With Moderate to Severe Crohn's Disease

Condition: Crohn's Disease  ·  Sponsor: Takeda

PhasePhase 3
Planned participants408
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

This is a study to evaluate vedolizumab for injection (300 mg) as a safe and active treatment for Crohn's Disease in adults in China. Participants will receive an injection of Vedolizumab 300 mg at scheduled weeks 0, 2, and 6, and starting at week 14, every 8 weeks over 58 weeks or starting at week 18, every 4 weeks over 54 weeks. There will be up to 20 study visits over 58 weeks to complete assessments.

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

Talk to the study team

Takeda Contact  ·  +1-877-825-3327  ·  medinfoUS@takeda.com

Always discuss trial participation with your own doctor first.

Locations (41)

The Second Hospital of Anhui Medical UniversityHefei, Anhui, ChinaRecruiting
Yijishan Hospital of Wannan Medical CollegeWuhu, Anhui, ChinaRecruiting
Peking University First Hospital - Changqiao CampusBeijing, Beijing Municipality, ChinaCompleted
Peking University Third HospitalBeijing, Beijing Municipality, ChinaRecruiting
The First Affiliated Hospital of Fujian Medical UniversityFuzhou, Fujian, ChinaRecruiting
Lanzhou University Second HospitalLanzhou, Gansu, ChinaRecruiting
The First People's Hospital of FoshanFoshan, Guangdong, ChinaRecruiting
The First Affiliated Hospital, Sun Yat-sen University - MainGuangzhou, Guangdong, ChinaRecruiting
Guangzhou First People's HospitalGuangzhou, Guangdong, ChinaRecruiting
The Second Affiliated Hospital of Guangzhou Medical UniversityGuangzhou, Guangdong, ChinaRecruiting
The Third Affiliated Hospital, Sun Yat-Sen UniversityGuangzhou, Guangdong, ChinaCompleted
The Sixth Affiliated Hospital, Sun Yat-sen UniversityGuangzhou, Guangdong, ChinaRecruiting

+ 29 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05837897