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Completed Phase 3 Interventional Results available

OASIS-HAE: A Study to Evaluate the Safety and Efficacy of Donidalorsen (ISIS 721744 or IONIS-PKK-LRx) in Participants With Hereditary Angioedema (HAE)

ClinicalTrials.gov ID: NCT05139810

Public ClinicalTrials.gov record NCT05139810. 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 22, 2026, 12:13 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

A Phase 3 Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ISIS 721744 in Patients With Hereditary Angioedema (HAE)

Study identification

NCT ID
NCT05139810
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ionis Pharmaceuticals, Inc.
Industry
Enrollment
91 participants

Conditions and interventions

Interventions

  • Donidalorsen Drug
  • Placebo 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
Dec 2, 2021
Primary completion
Nov 8, 2023
Completion
Nov 8, 2023
Last update posted
Mar 5, 2025

2021 – 2023

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Ionis Investigative Site Scottsdale Arizona 85251
Ionis Investigative Site San Diego California 92122
Ionis Investigative Site Santa Monica California 90404
Ionis Investigative Site Walnut Creek California 94598
Ionis Investigative Site Colorado Springs Colorado 80907
Ionis Investigative Site Tampa Florida 33613
Ionis Investigative Site Kansas City Kansas 66205
Ionis Investigative Site Boston Massachusetts 02114
Ionis Investigative Site Ann Arbor Michigan 48109
Ionis Investigative Site St Louis Missouri 63110
Ionis Investigative Site Columbus Ohio 43235
Ionis Investigative Site Toledo Ohio 43617
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 36 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05139810, 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 Mar 5, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05139810 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →