A Phase 3b, prospective, open-label, multicenter, single treatment arm, continuation study of the safety and efficacy of TAK-755 (rADAMTS-13, also known as BAX 930/SHP655) in the prophylactic and on-demand treatment of subjects with severe congenital thrombotic thrombocytopenic purpura (cTTP; Upshaw Schulman Syndrome, or hereditary thrombotic thrombocytopenic purpura)
Latest Information Update: 04 Feb 2025
At a glance
- Drugs Apadamtase alfa (Primary) ; Apadamtase alfa (Primary)
- Indications Thrombotic thrombocytopenic purpura
- Focus Adverse reactions; Registrational
- Sponsors Baxalta Innovations GmbH; Takeda
Most Recent Events
- 10 Dec 2024 Results (n=6) presented at the 66th American Society of Hematology Annual Meeting and Exposition.
- 25 Nov 2024 According to a Takeda media release, data from this study will be presented at at the 66th American Society of Hematology (ASH) Annual Meeting being held December 7-10, 2024, in San Diego, California.
- 25 Nov 2024 According to a Takeda media release, company will present data from this study on pediatric patients with congenital thrombotic thrombocytopenic purpura (cTTP) at the 66th American Society of Hematology (ASH) Annual Meeting being held December 7-10, 2024, in San Diego, California.