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An Open-Label Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Efficacy, and Safety of a Single Dose of Tanruprubart (Also Commonly Known as ANX005) in Participants With Guillain-Barré Syndrome (GBS) (FORWARD Study)

Trial Profile

An Open-Label Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Efficacy, and Safety of a Single Dose of Tanruprubart (Also Commonly Known as ANX005) in Participants With Guillain-Barré Syndrome (GBS) (FORWARD Study)

Status: Not yet recruiting
Phase of Trial: Phase III

Latest Information Update: 17 Jun 2025

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At a glance

  • Drugs Tanruprubart (Primary)
  • Indications Guillain-Barre syndrome
  • Focus Pharmacodynamics; Pharmacokinetics
  • Acronyms FORWARD
  • Sponsors Annexon

Most Recent Events

  • 15 Jun 2025 Status changed from not stated to not yet recruiting.
  • 19 May 2025 New trial record
  • 12 May 2025 According to Annexon media release, Initiation of the tanruprubart FORWARD study expected in the second quarter of 2025. FDA meeting with the Center for Drug Evaluation and Research (CDER) scheduled for the second quarter of 2025 ahead of planned BLA submission.

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