The purpose of this study was to assess OS outcomes in pediatric (≥ 28 days of age at the time of HSCT-TMA diagnosis) and adult participants diagnosed with HSCT-TMA(referred to as TMA from hereon) within 52 weeks after HSCT and who were either complement inhibitor treatment naïve or had been treated with eculizumab.
Inclusion Criteria:
Exclusion Criteria:
The study included pediatric participants who were diagnosed with TMA within 52 weeks after an HSCT procedure and who were complement inhibitor treatment naïve
The study included pediatric participants who were diagnosed with TMA within 52 weeks after an HSCT procedure and who had been treated with eculizumab
The study included adult participants who were diagnosed with TMA within 52 weeks after an HSCT procedure and who were complement inhibitor treatment naïve
The study included adult participants who were diagnosed with TMA within 52 weeks after an HSCT procedure and who had been treated with eculizumab
Boston, Massachusetts 02215, United States
Saitama-shi, Saitama 330-8777, Japan
Study in Adult and Pediatric Patients With HSCT-TMA
Identification and Treatment of Thrombotic Microangiopathies in Allogeneic Stem Cell Transplants
Thrombotic Microangiopathy (TMA) Associated With Allogeneic Hematopoietic Stem Cell Transplantation (HSCT) In Adult Patients
Assessing the Incidence of Transplant Associated Thrombotic Microangiopathy (TA-TMA) in Adult Patients Undergoing Allogeneic Stem Cell Transplant (SCT)
Ravulizumab in Thrombotic Microangiopathy After Hematopoietic Stem Cell Transplant
International Registry and Biorepository for TMA(Thrombotic Microangiopathy)
Safety and Efficacy of Eculizumab in High-risk TA-TMA
Identification of Plasma Biomarkers for Early Diagnosis of Transplant-associated Thrombotic Microangiopathy