Surgical Procedures and Hemostatic Outcome in Patients with Hemophilia Receiving Concizumab Prophylaxis during the Phase 3 explorer7 and explorer8 Trials

Introduction Concizumab is an anti-tissue factor pathway inhibitor monoclonal antibody that has been developed for once-daily subcutaneous prophylactic treatment for hemophilia of all subtypes. The phase 3 explorer7 (NCT04083781) and explorer8 trials (NCT04082429) investigated the efficacy and safety of concizumab prophylaxis in patients with hemophilia A or B with (HAwI/HBwI, explorer7) or without (HA/HB, explorer8) inhibitors. Aim To provide an overview of any surgical procedures at the 56-week cut-off performed on patients who received concizumab prophylaxis in the explorer7 and explorer8 trials. Methods Patients in both explorer7 and explorer8 trials were exposed to no prophylaxis (arm 1) or concizumab prophylaxis (arms 2-4) based on their treatment regimen before the trial. After the main part of the trial, all patients (arms 1-4) could continue in the extension part of the trial receiving concizumab for up to 136 weeks. Informed consent/ethics committee approvals were obtained as appropriate. Minor surgical procedures (defined as any invasive operative procedure where only the skin, mucous membranes or superficial connective tissue is manipulated) were permitted during the explorer7 and explorer8 trials, and management of minor surgeries was at the investigator's discretion. Planned major surgery was not permitted, and for any cases of acute major surgery, a concizumab pause was recommended. Data regarding both minor and major surgeries undertaken in patients were collected at the 56-week cut-off of the trials. Local/topical use of anti-fibrinolytics was permitted during surgical procedures in both trials (single systemic doses allowed following benefit-risk evaluation) and patients undergoing minor surgical procedures continued to receive concizumab prophylaxis during the perioperative period (with no change to the dosage they received). Results During both trials, a total of 278 patients received concizumab prophylaxis. Of these, 30 patients underwent a minor surgical procedure, including 6 (20.0%) adolescents (aged 12-17 years) and 24 (80.0%) adults (aged 18-64 years). Nine patients who underwent a minor procedure had HA (30.0%), 10 had HB (33.3%), 7 had HAwI (23.3%) and 4 had HBwI (13.3%). Four patients underwent both major and minor surgeries and 2 patients underwent major surgeries only. In total, 44 surgical procedures were undergone in 32 patients. The surgical procedures that were performed in patients who received concizumab included a rang