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Active, not recruiting Phase 3 Interventional

A Study to Assess the Long-Term Safety and Efficacy of Donidalorsen in the Prophylactic Treatment of Hereditary Angioedema (HAE)

ClinicalTrials.gov ID: NCT05392114

Public ClinicalTrials.gov record NCT05392114. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 12:37 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label, Long Term Safety and Efficacy Study of Donidalorsen in the Prophylactic Treatment of Hereditary Angioedema (HAE)

Study identification

NCT ID
NCT05392114
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ionis Pharmaceuticals, Inc.
Industry
Enrollment
154 participants

Conditions and interventions

Interventions

  • Donidalorsen Drug

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 12, 2022
Primary completion
Nov 30, 2026
Completion
Feb 28, 2027
Last update posted
Dec 11, 2025

2022 – 2027

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Ionis Investigative Site Paradise Valley Arizona 85253
Ionis Investigative Site La Jolla California 92037
Ionis Investigative Site Santa Monica California 90404
Ionis Investigative Site Walnut Creek California 94598
Ionis Investigative Site Tampa Florida 33613
Ionis Investigative Site Kansas City Kansas 66103
Ionis Investigative Site Boston Massachusetts 02114
Ionis Investigative Site Ann Arbor Michigan 48109
Ionis Investigative Site Detroit Michigan 48202
Ionis Investigative Site St Louis Missouri 63141
Ionis Investigative Site Mooresville North Carolina 28117
Ionis Investigative Site Cincinnati Ohio 45236
Ionis Investigative Site Columbus Ohio 43235
Ionis Investigative Site Hershey Pennsylvania 17033
Ionis Investigative Site Dallas Texas 75231
Ionis Investigative Site Murray Utah 84107

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 34 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05392114, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 11, 2025 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05392114 live on ClinicalTrials.gov.

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