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RecruitingPhase 3

Donidalorsen Treatment in Children With Hereditary Angioedema

Ionis Pharmaceuticals, Inc. · NCT07298447

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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

Study contacts (from the official record)

  • Ionis Pharmaceuticals, Inc. · (844) 201-3192 · IonisDonidalorsenPediatric@clinicaltrialmedia.com
Donidalorsen Treatment in Children With Hereditary Angioedema (NCT07298447) | Bored Studies