Commentary
Video
Author(s):
Matino discussed data from the phase 3 BASIS study evaluating the recently approved Hympavzi.
Marstacimab (Hympavzi; Pfizer) decreased the total number of bleeds and the severity of bleeds in treated patients with hemophilia A or B without inhibitors.1
These findings, from the phase 3 BASIS study, were presented at the 66th American Society of Hematology (ASH) Annual Meeting and Exposition, held December 7-10, 2024, in San Diego, California, by Davide Matino, MD, associate professor of medicine, McMaster University (MU), MU Medical Center Hemophilia Clinic, and Thrombosis Clinic at the Juravinski Hospital.
Marstacimab is an anti-tissue factor pathway inhibitor that was approved by the FDA in October for preventing or reducing bleeding episodes in patients with hemophilia A and B.2 The therapy is given weekly by an autoinjector pen and is the first subcutaneous option for those with hemophilia B in the United States. The ongoing BASIS is evaluating marstacimab in patients between the ages of 12 and 75 with severe hemophilia A or moderately severe to severe hemophilia B.1
“Each one of these new therapies could have a very specific space because of their very peculiar characteristics, mode of action, or in reducing the burden of the treatment for some patients, or because of the specific needs of some patients. So, I think it's this evolution. I think it's very welcome for both the from both the treaters perspective and the patient's perspective,” Matino told HCPLive® during the meeting, commenting on recent approvals of novel therapies for both hemophilia A and B.