At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 20 enrolled
Drug / intervention
Donidalorsendrug
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.
An Open-Label Extension Study of ISIS 721744 in Patients With Hereditary Angioedema
In Brief
A Phase 2 clinical trial evaluating Donidalorsen for Hereditary Angioedema. Completed, enrolled 20 participants across 7 sites in 2 countries.
Detailed Summary
The purpose of this study was to evaluate the safety and efficacy of extended dosing of donidalorsen administered subcutaneously (SC), with alternative dosing and/or dose frequency with donidalorsen in participants with hereditary angioedema (HAE).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHereditary Angioedema
CountriesNetherlands, United States
Collaborators--
Timeline
Phase 2CompletedFinished
202120222023202420252026
First PostedMar 2020
Enrollment StartMar 2020
Primary CompletionJan 2025
TodayJul 2026
First PostedMar 13, 2020
Enrollment StartMar 31, 2020
Primary CompletionJan 24, 2025
TodayJul 2, 2026
Enrollment to primary: 4.8 yearsPosted 6.3 years ago
Interventions
Donidalorsendrug
Donidalorsen administered SC