A MULTICENTER, OPEN-LABEL, NON-RANDOMIZED, PHASE III STUDY TO EVALUATE THE SAFETY, EFFICACY, PHARMACOKINETICS, AND PHARMACODYNAMICS OF EMICIZUMAB IN PATIENTS WITH ACQUIRED HEMOPHILIA A
Latest Information Update: 30 Jan 2023
At a glance
- Drugs Emicizumab (Primary)
- Indications Haemophilia A
- Focus Adverse reactions; Registrational
- Acronyms AGEHA
- Sponsors Chugai Pharmaceutical
- 22 Dec 2022 Results (at data cut-off: 23 April 2021; n=11) assessing efficacy, safety, and pharmacokinetics of emicizumab in patients with acquired hemophilia a, published in the Journal of Thrombosis and Haemostasis.
- 13 Dec 2022 Results assessing population pharmacokinetic analysis of emicizumab in patients with acquired hemophilia a, presented at the 64th American Society of Hematology Annual Meeting and Exposition
- 13 Dec 2022 Additional safety and efficacy results collected after cutoff date of the primary analysis presented at the 64th American Society of Hematology Annual Meeting and Exposition