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A Phase 2, Open-Label, Repeat Dose Study to Assess the Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) of Intravenous ANX005 in Subjects With Warm Autoimmune Hemolytic Anemia (wAIHA)

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Trial Profile

A Phase 2, Open-Label, Repeat Dose Study to Assess the Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) of Intravenous ANX005 in Subjects With Warm Autoimmune Hemolytic Anemia (wAIHA)

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 17 Jun 2024

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At a glance

  • Drugs Tanruprubart (Primary)
  • Indications Haemolytic anaemia
  • Focus Adverse reactions; Proof of concept; Therapeutic Use
  • Sponsors Annexon

Most Recent Events

  • 03 Mar 2023 Status changed from recruiting to completed.
  • 09 Feb 2023 This trial has been completed in Bulgaria and Austria (Global end date: 17 Jan 2023).
  • 01 Feb 2023 The trial has been completed in Germany, according to European Clinical Trials Database record.

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