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Clinical trial

An Open-label, Phase 3 Study to Evaluate the Efficacy, Safety and Pharmacokinetics of 0.05 mg/kg/Day Subcutaneous Teduglutide Following Treatment of Short Bowel Syndrome for 24 Weeks in Chinese Adults Who Are Dependent on Parenteral Support

NCT06973304 is registered in ClinicalTrials.gov with Takeda as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
An Open-label, Phase 3 Study to Evaluate the Efficacy, Safety and Pharmacokinetics of 0.05 mg/kg/Day Subcutaneous Teduglutide Following Treatment of Short Bowel Syndrome for 24 Weeks in Chinese Adults Who Are Dependent on Parenteral Support
Lead sponsor
Takeda
Phase
Phase 3
Overall status
Active, not recruiting
Start date
June 26, 2025
Completion date
July 28, 2027
Enrollment
13 (actual)
Sites
4

Conditions

As the registry lists them; a condition with its own page is linked.