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A Phase 3, Multicenter, Randomized, Placebo-controlled, Double-blind Study to Evaluate the Efficacy and Safety of Lanadelumab for Prevention Against Acute Attacks of Non-histaminergic Angioedema with Normal C1-Inhibitor (C1-INH) and Acquired Angioedema (AAE) Due to C1-INH Deficiency

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Trial Profile

A Phase 3, Multicenter, Randomized, Placebo-controlled, Double-blind Study to Evaluate the Efficacy and Safety of Lanadelumab for Prevention Against Acute Attacks of Non-histaminergic Angioedema with Normal C1-Inhibitor (C1-INH) and Acquired Angioedema (AAE) Due to C1-INH Deficiency

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 10 Oct 2024

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At a glance

  • Drugs Lanadelumab (Primary) ; Icatibant
  • Indications Acquired angioedema; Hereditary angioedema
  • Focus Registrational; Therapeutic Use
  • Sponsors Shire; Takeda; Takeda Development Center Americas

Most Recent Events

  • 19 Dec 2022 This trial has been completed in Hungary according to European Clinical Trials Database record.
  • 24 Oct 2022 Status changed from active, no longer recruiting to completed.
  • 16 Oct 2022 This trial has been completed in Poland according to European Clinical Trials Database record.

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