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Search / Trial NCT05023382

A Study of Teduglutide in Japanese People With Short Bowel Syndrome

Launched by TAKEDA · Aug 23, 2021

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying a medication called teduglutide (also known as Revestive) to see how well it helps people with Short Bowel Syndrome (SBS) and to check for any side effects. Short Bowel Syndrome is a condition that affects the body's ability to absorb nutrients because of a shortened intestine. The trial is open to anyone in Japan who has been treated with teduglutide, and there are no specific exclusions, which means most people with this condition can participate.

During the study, participants will receive injections of teduglutide just under the skin, and doctors will monitor them for side effects for up to three years. Since this is a post-marketing surveillance study, it aims to gather more information about the medication's effects in a real-world setting, outside of the initial clinical trials. If you or a loved one is interested in participating, you could help researchers understand how well this treatment works for people living with Short Bowel Syndrome.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • All participants in Japan who received teduglutide will be enrolled in this post marketing surveillance.
  • Exclusion Criteria:
  • None

About Takeda

Takeda Pharmaceutical Company Limited is a global, research-driven biopharmaceutical organization committed to advancing patient care through innovative therapies. Founded in 1781 and headquartered in Osaka, Japan, Takeda focuses on key therapeutic areas including oncology, gastroenterology, neuroscience, and rare diseases. With a strong emphasis on research and development, Takeda leverages cutting-edge science and technology to deliver transformative medicines that address unmet medical needs. The company is dedicated to sustainability and ethical practices, ensuring that its clinical trials uphold the highest standards of safety and efficacy while fostering collaboration with healthcare professionals and communities worldwide.

Locations

Tokyo, , Japan

Patients applied

0 patients applied

Trial Officials

Study Director

Study Director

Takeda

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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