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Search / Trial NCT06590974

A Study of Freeze-dried Human Protein C Concentrate (TAK-662) in Participants with Congenital Protein C Deficiency

Launched by TAKEDA · Sep 5, 2024

Trial Information

Current as of July 01, 2025

Recruiting

Keywords

Ceprotin/Protein C Deficiency

ClinConnect Summary

This clinical trial is studying a new treatment called Freeze-dried Human Protein C Concentrate, or TAK-662, for people with a condition known as congenital protein C deficiency. This condition means the body does not produce enough protein C, which is important for blood clotting. The main goal of the study is to see how well TAK-662 works and to monitor any side effects that might occur during treatment.

If you or a family member has congenital protein C deficiency and are interested in participating, you may be eligible as there are no specific exclusion criteria. Participants will receive TAK-662 through an intravenous (IV) injection, and the researchers will observe and record any effects for up to 24 months. This study is currently recruiting participants of all ages and genders, and it aims to gather valuable information about the safety and effectiveness of this treatment for those living with this condition.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • - All participants with congenital protein C deficiency who are administered with Freeze-dried Human Protein C Concentrate (TAK-662).
  • 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