At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 11 enrolled
Drug / intervention
Wilatedrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Clinical Study to Investigate the Pharmacokinetics, Efficacy, Safety, and Immunogenicity of Wilate in Previously Treated Paediatric Patients With Severe Haemophilia A
In Brief
A Phase 3 clinical trial evaluating Wilate for Severe Hemophilia A. Completed, enrolled 11 participants across 3 sites in 2 countries.
Detailed Summary
A prospective, non-controlled, international, multi-centre phase 3 study to investigate the pharmacokinetics, efficacy, safety, and immunogenicity of Wilate in previously treated children with severe haemophilia A
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSevere Hemophilia A
CountriesRussia, Ukraine
Collaborators--
Timeline
Phase 3CompletedFinished
201820192020202120222023202420252026
Enrollment StartNov 2017
First PostedDec 2017
Primary CompletionNov 2018
TodayJul 2026
First PostedDec 18, 2017
Enrollment StartNov 22, 2017
Primary CompletionNov 3, 2018
TodayJul 2, 2026
Enrollment to primary: 11 monthsPosted 8.5 years ago
Interventions
Wilatedrug
von Willebrand factor / Factor VIII (plasma derived)