Retrospective Analysis of the Efficiency of Caplacizumab in the Treatment of Acquired Thrombotic Thrombocytopenic Purpura (aTTP)- REACT-2020

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Observational
SUMMARY

The objective of this national, prospective, multi-centre observational study is to describe the prescription rational and practice in Germany, confirm the efficacy of caplacizumab in a real-world setting, and identify predicting factors in iTTP-patients with regard to persistent autoimmune activity, therapy guidance and risk of complications. The rational is to develop new treatment algorithms that optimize overall patient outcome and reduce treatment cost.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Confirmed diagnosis of an acute episode of acquired thrombotic thrombocytopenic purpura

• Treatment with at least one single dose of caplacizumab (10 mg i.v. or s.c.)

• Male or female patients ≥ 18 years of age

• signed written informed consent

Locations
Other Locations
Germany
University Hospital of Cologne
RECRUITING
Cologne
Contact Information
Primary
Linus Völker, MD
linus.voelker@uk-koeln.de
+49 221 478 86285
Backup
Lucas Kühne, MD
lucas.kuehne@uk-koeln.de
Time Frame
Start Date: 2021-03-25
Estimated Completion Date: 2034-12-12
Participants
Target number of participants: 350
Treatments
Registergroup
Patients with acquired Thrombotic Thrombocytopenic Purpura, who have been treated with caplacizumab (Cablivi®)
Related Therapeutic Areas
Sponsors
Leads: University of Cologne

This content was sourced from clinicaltrials.gov