Donidalorsen Expanded Access Program for Patients With Hereditary Angioedema

NCT06415448 · Status: AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2025-07-11

No results posted yet for this study

Summary

The purpose of the Expanded Access Program is to provide pre-approval access of donidalorsen to eligible patients with Hereditary Angioedema (HAE) who complete the ISIS 721744-CS3 clinical trial.

Conditions

Interventions

DRUG

Donidalorsen

Donidalorsen administered once monthly or every other month by subcutaneous (SC) injections in the abdomen, thigh, or upper arm.

Sponsors & Collaborators

  • Ionis Pharmaceuticals, Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06415448 on ClinicalTrials.gov