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Clinical Trial ● Currently Recruiting Phase III NCT07428499

Phase 3 Extension Study of ADX-324 in Participants With Hereditary Angioedema (HAE)

Phase 3 Extension Study of ADX-324 in Participants With Hereditary Angioedema (HAE) — Recruiting • Phase III • Cardiology / Cardiovascular • NCT07428499.

📅 30 Apr 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT07428499
Sponsor
ADARx Pharmaceuticals, Inc.
Start
2026-04-02
ClinicaliQ Trial Snapshot
  • Phase 3 Extension Study of ADX-324 in Participants With Hereditary Angioedema (HAE) — Recruiting • Phase III • Cardiology / Cardiovascular • NCT07428499.
  • Treatment being tested: ADX-324 is a novel therapy being evaluated for long-term safety and efficacy in hereditary angioedema (HAE) Types I and II, building on data from the completed Phase 3 ADX-324-301 trial through this extension study.
  • Patient eligibility: The study enrolls participants who have successfully completed the preceding Phase 3 ADX-301 trial, ensuring a well-characterised population with confirmed HAE Types I or II and documented tolerance of the investigational drug.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

Study ADX-324-302 is an extension study for participants who complete the Phase 3 ADX-324-301 trial. The extension study will provide information about the safety and efficacy of additional dosing of ADX-324 in participants with Type I and Type II hereditary angioedema (HAE). The study will also include pharmacodynamic (PD), pharmacokinetic (PK), and health-related quality of life (HRQoL) measurements.

Eligibility Snapshot
  • : * Have a documented diagnosis of HAE (Type I or II) * Completed Study ADX-324-301 * Have access to an acute therapy to treat HAE attacks (such as plasma derived or recombinant C1-INH concentrate or a BK2-receptor antagonist)

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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