An Open-label, Single Arm, Multi-centre, Phase II Study Investigating Safety, Tolerability, Efficacy, Pharmacodynamics and Pharmacokinetics of Imlifidase in Patients With Guillain-Barré Syndrome, in Comparison With Matched Control Patients
Latest Information Update: 20 Dec 2024
At a glance
- Drugs Imlifidase (Primary)
- Indications Guillain-Barre syndrome
- Focus Adverse reactions; Proof of concept; Therapeutic Use
- Acronyms 15HMedIdeS09
- Sponsors Hansa Biopharma AB
- 17 Dec 2024 Full Results presented in the Hansa Biopharma AB media release.
- 17 Oct 2024 According to a Hansa Biopharma AB media release, data read-out expected by year end 2024.
- 08 Jun 2024 This study has been Completed in Netherlands, According to European Clinical Trials Database record.