thrombotic thrombocytopenic purpura

Search with Google Search with Bing
Information
Disease name
thrombotic thrombocytopenic purpura
Disease ID
DOID:10772
Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT01931644 Completed At-Home Research Study for Patients With Autoimmune, Inflammatory, Genetic, Hematological, Infectious, Neurological, CNS, Oncological, Respiratory, Metabolic Conditions July 2013 April 2024
NCT01554514 Completed Phase 2 Low Dose Rituximab in Thrombotic Thrombocytopenic Purpura August 2012 February 14, 2020
NCT00426686 Completed ADAMTS13 in Thrombotic Thrombocytopenic Purpura November 2006 April 2011
NCT04074187 Completed Phase 2/Phase 3 A Trial of Caplacizumab in Japanese Patients With Acquired Thrombotic Thrombocytopenic Purpura (aTTP) October 21, 2019 May 19, 2021
NCT00713193 Completed Phase 3 Study of Cyclosporine or Corticosteroids as an Adjunct to Plasma Exchange in Thrombotic Thrombocytopenic Purpura (TTP) November 2007 September 20, 2017
NCT03369314 Completed Observational Study of the Use of octaplasLG®. March 2, 2018 January 14, 2021
NCT02134171 Completed N/A Early Predictive Factors of Cardiac and Cerebral Involvement in TMA June 10, 2014 July 30, 2017
NCT00907751 Completed Phase 2 Rituximab in Adult Acquired Idiopathic Thrombotic Thrombocytopenic Purpura May 2010 August 2013
NCT05568147 Not yet recruiting Phase 2/Phase 3 Aspirin for Prophylaxis of TTP October 1, 2022 September 30, 2028
NCT05785468 Recruiting A Retrospective, Observational Study on the Response to Caplacizumab Treatment in aTTP Patients: the Italian Experience (ROSCAPLI) October 21, 2021 March 30, 2023
NCT01257269 Recruiting Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome) October 2006 October 2030
NCT03187652 Recruiting A Prospective Study on the Long-Term Vascular Burden in Thrombotic Thrombocytopenic Purpura Patients January 1, 2017 January 1, 2026
NCT05389007 Recruiting .German TTP-Registry (Thrombotic Thrombocytopenic Purpura) July 8, 2016
NCT05468320 Recruiting Phase 3 Caplacizumab and Immunosuppressive Therapy Without Firstline Therapeutic Plasma Exchange in Adults With Immune-mediated Thrombotic Thrombocytopenic Purpura November 21, 2022 December 13, 2024
NCT00593229 Terminated International Registry and Biorepository for TMA(Thrombotic Microangiopathy) January 2007
NCT01938404 Terminated Octaplas Adult TTP Trial June 6, 2017 August 2, 2017
NCT00726544 Terminated Phase 2 Clinical Outcome Study of ARC1779 Injection in Patients With Thrombotic Microangiopathy December 2008 March 2011
NCT00799773 Terminated Phase 3 Evaluating the Effectiveness of Adding Rituximab to Standard Treatment for Thrombotic Thrombocytopenic Purpura (TTP) April 2009 February 2010
NCT00953771 Terminated Phase 2 Safety Study of Danazol With Plasma Exchange and Steroids for the Treatment of Thrombotic Thrombocytopenic Purpura (TTP) October 2008 November 19, 2015
NCT04588194 Unknown status Phase 2 Romiplostim, Rituximab and Dexamethasone as Frontline Treatment for Immune Thrombocytopenia November 1, 2020 November 1, 2022
NCT03237819 Unknown status Phase 3 Magnesium Sulfate in Thrombotic Thrombocytopenic Purpura in Intensive Care May 27, 2018 December 1, 2021
NCT03605511 Unknown status TTP and aHUS in Complicated Pregnancies September 21, 2018 March 14, 2020
NCT04981028 Unknown status The ConNeCT Study: Neurological Complications of TTP June 25, 2020 June 25, 2022
NCT00531089 Unknown status Phase 2 Rituximab in Patients With Relapsed or Refractory TTP-HUS December 2007 January 2011
NCT02626663 Withdrawn The Role of Microparticles as a Biomarker July 2016 December 2022
NCT00251277 Withdrawn Phase 1/Phase 2 Use of Rituximab Treatment in Addition to Standard Care for Newly Presenting Thrombotic Thrombocytopenic Purpura November 2005 April 2009
Disase is a (Disease Ontology)
DOID:2452
Cross Reference ID (Disease Ontology)
GARD:9430
Cross Reference ID (Disease Ontology)
ICD10CM:M31.19
Cross Reference ID (Disease Ontology)
MESH:D011697
Cross Reference ID (Disease Ontology)
MIM:274150
Cross Reference ID (Disease Ontology)
NCI:C78797
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:360402008
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0034155
Exact Synonym (Disease Ontology)
Moschcowitz's syndrome
OrphaNumber from OrphaNet (Orphanet)
54057