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A Phase III Study to Evaluate the Efficacy of INM004 (Shiga Antitoxin) in Pediatric Patients With Shiga Toxin-producing Escherichia Coli-associated Hemolytic Uremic Syndrome

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Trial Profile

A Phase III Study to Evaluate the Efficacy of INM004 (Shiga Antitoxin) in Pediatric Patients With Shiga Toxin-producing Escherichia Coli-associated Hemolytic Uremic Syndrome

Status: Recruiting
Phase of Trial: Phase III

Latest Information Update: 04 Mar 2025

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At a glance

  • Drugs INM 004 (Primary)
  • Indications Haemolytic uraemic syndrome
  • Focus Registrational; Therapeutic Use
  • Sponsors Inmunova

Most Recent Events

  • 05 Aug 2024 Planned initiation date changed from 16 Jun 2024 to 17 Aug 2024.
  • 05 Aug 2024 Status changed from not yet recruiting to recruiting.
  • 27 May 2024 Planned initiation date changed from 16 May 2024 to 16 Jun 2024.

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