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Retrospective Study on Caplacizumab-treated Pediatric Patients With Immune-mediated Thrombocytopenic Purpura (iTTP)

Completed
Conditions
Immune-mediated Thrombocytopenic Purpura
Registration Number
NCT05263193
Lead Sponsor
Sanofi
Brief Summary

The purpose of this multi-country, retrospective data collection study (chart review) is to describe the effectiveness and safety of caplacizumab in pediatric patients with iTTP.

Detailed Description

Pediatric patients who received caplacizumab will be identified for enrollment in the chart review. The eligibility period starts on August 30, 2018 in the United Kingdom (UK) and France and February 6, 2019 for the United States (US).

Data collection is fully retrospective and will be anchored to the patient's index event date. The index event date is defined as the date the patient initiated caplacizumab treatment. The study period begins at the index date and ends at the earliest date of chart abstraction initiation, 12 weeks after last dose of caplacizumab treatment, date of death, or loss to follow-upwhich ever comes first .

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
4
Inclusion Criteria
  • Patient's aged ≤18 years at start of caplacizumab treatment initiation
  • Patient has a diagnosis of iTTP documented in the medical records
  • Patient was treated with caplacizumab within the eligibility period
Exclusion Criteria
  • Patient declined use of data for study (where local regulations require patient notification of planned study)
  • Patient's medical chart is missing or not retrievable

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Proportion of subjects with recurrent diseaseFrom index date up to 12 weeks after last dose of caplacizumab

Proportion of subjects with iTTP exacerbation (defined as recurrence within 30 days after last PE) and Proportion of subjects with iTTP relapse (defined as recurrence more than 30 days after last PE)

Total duration of hospitalization staysFrom index date up to 12 weeks after last dose of caplacizumab
Proportion of patients achieving clinical responseFrom index date up to 12 weeks after last dose of caplacizumab

defined as a normal platelet countand LDH \< 2 ULN for at least 48 hours following initial normalization or response of platelet count

Platelet count responseFrom index date up to 12 weeks after last dose of caplacizumab

defined as time from caplacizumab initiation to initial platelet count ≥ 150×109/L with subsequent stop of daily plasma exchange (PE) within 5 days

Proportion of subjects with refractory iTTPFrom index date up to 12 weeks after last dose of caplacizumab

defined as lack of doubling of platelet count after four days of caplacizumab treatment and a lactate dehydrogenase (LDH) level that remained above the upper limit of normal (ULN) range

Number of participants with Adverse eventFrom index date up to 12 weeks after last dose of caplacizumab

including serious adverse events

Time to normalization of organ damage marker levelsFrom index date up to 12 weeks after last dose of caplacizumab

Defined asLDH ≤ 2 x ULN, Serum creatinine ≤ 1 x ULN, Cardiac troponin I ≤ 1 x ULN

Duration of therapeutic PEFrom index date up to 12 weeks after last dose of caplacizumab
Time to ADAMTS13 activity ≥ 20%From index date up to 12 weeks after last dose of caplacizumab

where available and feasible

Duration of intensive care unit (ICU) stayFrom index date up to 12 weeks after last dose of caplacizumab
Secondary Outcome Measures
NameTimeMethod
Treatment pattern of caplacizumab therapyFrom index date up to 12 weeks after last dose of caplacizumab

Dosing and duration

Types and duration of concomitant medicationsFrom index date up to 12 weeks after last dose of caplacizumab

Trial Locations

Locations (1)

Sanofi-Aventis

🇫🇷

Chilly-Mazarin, France

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