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Concizumab Reduces Bleeding in Hemophilia with Inhibitors: Median ABR 0.8 at 56 Weeks

Key Takeaway
Consider concizumab for reducing bleeding in hemophilia A/B with inhibitors due to its proven efficacy.

The phase 3 explorer7 study evaluated the efficacy and safety of concizumab, an anti-TFPI monoclonal antibody, for prophylaxis in patients with hemophilia A or B with inhibitors (HAwI/HBwI). The study included 133 male patients aged ≥12 years, with 80 having hemophilia A and 53 having hemophilia B. Patients were randomized in a 1:2 ratio to either no prophylaxis (group 1) or concizumab prophylaxis (group 2), with additional nonrandomized groups (3 and 4) receiving concizumab. After a minimum of 24 weeks, patients in the no prophylaxis group were allowed to switch to concizumab. At the 56-week cutoff, the primary endpoint showed a significant reduction in the median annualized bleeding rate (ABR) for spontaneous and traumatic bleeding episodes in patients receiving concizumab, with a median ABR of 0.8 (IQR, 0.0-3.2), consistent with earlier results at the 32-week cutoff. Secondary endpoints included pharmacokinetics and pharmacodynamics, which demonstrated stable concizumab and free-TFPI concentrations over time. Safety analysis revealed no new adverse events, confirming the drug's safety profile. The study results support the longer-term efficacy and safety of concizumab prophylaxis in reducing bleeding episodes in HAwI/HBwI patients, providing a viable prophylactic option for this population.

AI Accuracy Review: 9/10 · Auto-published
View Original Abstract ↓
Concizumab is an anti-tissue factor pathway inhibitor (TFPI) monoclonal antibody intended for once-daily subcutaneous prophylactic treatment for people with hemophilia A or B with and without inhibitors. Results from the phase 3 explorer7 study confirmed superiority of concizumab prophylaxis over no prophylaxis in reducing the annualized bleeding rate (ABR) in people with hemophilia A or B with inhibitors (HAwI/HBwI). Male patients aged ≥12 years were randomized 1:2 to no prophylaxis (group 1) or concizumab prophylaxis (group 2), or nonrandomly allocated to concizumab prophylaxis (groups 3 and 4). After ≥24 weeks of treatment, patients in group 1 could switch to concizumab prophylaxis. At the 56-week cutoff (defined as when all patients in groups 2-4 had completed the visit at 56 weeks or permanently discontinued treatment), bleed-related efficacy, pharmacokinetics and pharmacodynamics, and safety were assessed. Of the 133 patients enrolled (HAwI, n = 80; HBwI, n = 53), 114 received concizumab prophylaxis (groups 2-4) and 19 were randomized to no prophylaxis (group 1). After ≥24 weeks, 13 patients from group 1 switched to concizumab. Median ABR for treated spontaneous and traumatic bleeding episodes in patients receiving concizumab was 0.8 (interquartile range [IQR], 0.0-3.2) at the 56-week cutoff, consistent with the low bleeding rates (median ABR, 0.0; IQR, 0.0-3.3) at the 32-week cutoff. Concizumab and free-TFPI concentration remained stable over time. No new safety concerns were reported. Longer-term (≥1 year) efficacy and safety results of concizumab prophylaxis for HAwI/HBwI were consistent with the 32-week cutoff results in explorer7. This trial was registered at www.clinicaltrials.gov as #NCT04083781.
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