Donidalorsen Treatment in Children With Hereditary Angioedema
Ionis Pharmaceuticals, Inc. · NCT07298447
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 2–11 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 20
- US sites recruiting
- 8
- Study start
- April 21, 2026
- Record last updated
- September 2, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics of donidalorsen in pediatric participants with hereditary angioedema (HAE) Type I (HAE-1) or Type II (HAE-2).
Being studied: Donidalorsen
Conditions: Hereditary Angioedema (HAE)
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Key Inclusion Criteria
- Must be between the ages of 2 and less than 12 years, inclusive, at the time of informed consent and, as applicable, assent.
- Must weigh at least 9 kg at the time of informed consent and, as applicable, assent.
- Documented diagnosis of HAE-1/HAE-2 based upon both of the following:
- Documented clinical history consistent with HAE (SC or mucosal, non-pruritic swelling episodes without accompanying urticaria).
- Diagnostic testing results that confirm HAE-1/HAE-2: C1-inhibitor (C1-INH) functional level \<50% normal level AND complement factor C4 level below the lower limit of normal (LLN); OR a known pathogenic mutation in the SERPING1 gene.
Key Exclusion Criteria
- Must not have any screening laboratory abnormalities or any other clinically significant abnormalities during screening that would render a participant unsuitable for inclusion.
- Must not have been treated with another investigational drug, biological agent, or device within 1 month of Screening, or 5 half-lives of investigational agent, whichever is longer.
- Concurrent diagnosis of any other type of recurrent angioedema, including idiopathic angioedema or HAE with normal C1-INH (HAE-nC1-INH or Type III).
Note: Other protocol-specified inclusion/exclusion criteria may apply.
Recruiting US locations
Ionis Investigative Site
Santa Monica, CA 90404
Ionis Investigative Site
Miami, FL 33136
Ionis Investigative Site
Baton Rouge, LA 70809
Ionis Investigative Site
St Louis, MO 63141
Ionis Investigative Site
Cincinnati, OH 45236
Ionis Investigative Site
Cleveland, OH 44195
Ionis Investigative Site
Hershey, PA 17033
Ionis Investigative Site
West Allis, WI 53214
Study contacts (from the official record)
- Ionis Pharmaceuticals, Inc. · (844) 201-3192 · IonisDonidalorsenPediatric@clinicaltrialmedia.com