Post-Marketing Surveillance To Observe Safety And Efficacy Of Xyntha Solofuse Prefilled Syringe

Hemophilia A, Congenital Clinical Trial

Official title: POST-MARKETING SURVEILLANCE TO OBSERVE SAFETY AND EFFICACY OF XYNTHA SOLOFUSE PREFILLED SYRINGE

Status Completed

Clinical Trial Summary

This study aims to observe the safety and efficacy of the Xyntha Solofuse prefilled syringe in the setting of routine practice. The primary objective is to detect medically significant events (factor VIII inhibitor). The secondary objective is to observe the overall efficacy and safety of the Xyntha Solofuse prefilled syringe including serious adverse events. In this open-label, non-comparative, observational, non-interventional, retrospective and multi-center study, post-marketing surveillance data will be collected retrospectively for up to 6 months from the initial administration day of the Xyntha Solofuse prefilled syringe injected into patients who have been administered the Xyntha Solofuse prefilled syringe.

As specified in the product approval issued by the Ministry of Food and Drug Safety, the study will be conducted for 4 years from the approval date. At least 600 study subjects will be enrolled in this study to meet the MFDS requirements. Although 600 is the assigned number of study subjects, the number of cases will be adjusted considering the actual number of enrolled subjects after the study start day.

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Autosomal Hemophilia A
• Classic Hemophilia
• Factor 8 Deficiency, Congenital
• Factor VIII Deficiency, Congenital
• Hemophilia A
• Hemophilia A, Congenital

• NCT number: NCT03034044
• Study type: Observational
• Source: Pfizer
• Status: Completed
• Start date: January 2017
• Completion date: January 17, 2018