PREDICT2020: Platelet Response to Caplacizumab in the Treatment of Acquired Thrombotic Thrombocytopenic Purpura

Sponsor
University of Cologne (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05876221
Collaborator
(none)
160
1
12
13.3

Study Details

Study Description

Brief Summary

The interpretation of platelet counts has to be revaluated in the light of caplacizumab. By effectively blocking platelet binding sites on VWF-multimers, the nanobody leads to a rapid normalization of the platelet count within 3 to 4 days. Most importantly, caplacizumab uncouples platelet counts from ADAMTS13 activity and thereby launches unprecedented thrombocyte dynamics, with potential pitfalls for over- and undertreatment.

A relevant number of patients responds to caplacizumab with a brisk increase in platelet count, followed by a marked dip of platelets (patient on the left). This may mislead treating physicians into re-intensifying therapy, with a respective risk for adverse side-effects and complications. Taken together, these observations call for reliable descriptions and the identification of predictive parameters to predict the platelet response upon administration of caplacizumab in a large patient cohort. Here, PREDICT-2020 is designed as a retrospective study to specifically address the following aspects:

  • Identifying and describing clusters of platelet responses to caplacizumab

  • Identifying potential pitfalls for treating physicians

  • Predicting the individual thrombocyte response

  • Correlating platelet responses with individual patient outcome

Condition or Disease Intervention/Treatment Phase

Study Design

Study Type:
Observational
Anticipated Enrollment :
160 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Platelet Response to Caplacizumab in the Treatment of Acquired Thrombotic Thrombocytopenic Purpura
Anticipated Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Jun 30, 2024
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
aTTP-Patients

Patients with immune Thrombotic Thrombocytopenic Purpura, who have been treated with caplacizumab (Cablivi®)

Drug: Cablivi
Patients with immune Thrombotic Thrombocytopenic Purpura, who have been treated with caplacizumab (Cablivi®)

Outcome Measures

Primary Outcome Measures

  1. Reliable description and prediction of platelet responses to caplacizumab [Enrollment]

    Reliable description and prediction of platelet responses to caplacizumab employing mathematic modelling algorithms

Secondary Outcome Measures

  1. Determination of different clusters of platelet responses to caplacizumab [Enrollment]

    It will be hypothesized the existence of different clusters of caplacizumab responders during the first weeks of therapy, when ADAMTS13 activity typically is still <10%. A detailed cluster analysis and description of thrombocyte responses to caplacizumab in a large cohort will reliably identify these different responders

  2. Correlation of platelet responses to caplacizumab with patient outcome [Enrollment]

    It will be hypothesized the existence of different clusters of caplacizumab responders during the first weeks of therapy, when ADAMTS13 activity typically is still <10%. A detailed cluster analysis and description of thrombocyte responses to caplacizumab in a large cohort will reliably identify these different responders

  3. Risk stratification of iTTP patients based on their platelet response to caplacizumab [Enrollment]

    Description: Predicting the individual thrombocyte response to caplacizumab improves risk stratification of iTTP patients after initiation of caplacizumab therapy. An early risk stratification allows an optimal timing of monitoring intervals during the first weeks after diagnosis, which are often critical

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Confirmed diagnosis of autoimmune thrombotic thrombocytopenic purpura

  • Treatment with at least a single dose of caplacizumab, either i.v. or s.c.

  • Male or female patients older than 18 years of age

Exclusion Criteria:
  • Hereditary thrombotic thrombocytopenic purpura

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospital of Cologne Cologne Germany

Sponsors and Collaborators

  • University of Cologne

Investigators

  • Principal Investigator: Lucas Kühne, MD, Department II of Internal Medicine, University Hospital of Cologne

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Prof. Dr. Paul Brinkkoetter, Consultant in Nephrology, University of Cologne
ClinicalTrials.gov Identifier:
NCT05876221
Other Study ID Numbers:
  • 2020-11-17
First Posted:
May 25, 2023
Last Update Posted:
May 30, 2023
Last Verified:
May 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Prof. Dr. Paul Brinkkoetter, Consultant in Nephrology, University of Cologne
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 30, 2023