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An Open-Label Study of Donidalorsen in Pediatric Patients Age 2 to Less than 12 Years Old with Hereditary Angioedema [Donidalorsen Treatment in Children with Hereditary Angioedema]

Status
Not yet recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-523499-22-00
Enrollment
6
Registered
2026-02-25
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hereditary Angioedema (HAE)

Brief summary

1. Incidence and severity of treatment-emergent adverse events (TEAEs), 2. Plasma pharmacokinetics and concentrations of donidalorsen

Detailed description

1. The time-normalized number of investigator-confirmed HAE attacks (per month) over the period of 12 months., 3. The percentage of investigator-confirmed HAE attack-free participants over the period of 12 months., 4. The time-normalized number of moderate or severe investigatorconfirmed HAE attacks (per month) over the period of 12 months., 5. The number of participants with a clinical response defined as a ≥ 50%, ≥ 70%, or ≥ 90% reduction from Baseline in investigator-confirmed HAE attack rate over the period of 12 months., 6. The number of investigator-confirmed HAE attacks requiring rescue treatment (i.e., acute therapy) over the period of 12 months., 7. Change in PKK levels in plasma over the period of 12 months., 8. Changes in Pediatrics Quality of Life (PedsQL) scores for participants over the period of 12 months.

Interventions

Sponsors

Ionis Pharmaceuticals Inc.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
0 Years to 17 Years

Design outcomes

Primary

MeasureTime frame
1. Incidence and severity of treatment-emergent adverse events (TEAEs), 2. Plasma pharmacokinetics and concentrations of donidalorsen

Secondary

MeasureTime frame
1. The time-normalized number of investigator-confirmed HAE attacks (per month) over the period of 12 months., 3. The percentage of investigator-confirmed HAE attack-free participants over the period of 12 months., 4. The time-normalized number of moderate or severe investigatorconfirmed HAE attacks (per month) over the period of 12 months., 5. The number of participants with a clinical response defined as a ≥ 50%, ≥ 70%, or ≥ 90% reduction from Baseline in investigator-confirmed HAE attack rate over the period of 12 months., 6. The number of investigator-confirmed HAE attacks requiring rescue treatment (i.e., acute therapy) over the period of 12 months., 7. Change in PKK levels in plasma over the period of 12 months., 8. Changes in Pediatrics Quality of Life (PedsQL) scores for participants over the period of 12 months.

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 27, 2026