- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Acquired Thrombotic Thrombocytopenic Purpura.
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EudraCT Number: 2010-018794-38 | Sponsor Protocol Number: RTXTTP2010 | Start Date*: 2010-02-23 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS CA` GRANDA OSPEDALE MAGGIORE POLICLINICO DI MILANO | |||||||||||||
Full Title: EVALUATION OF CLINICAL RESPONSE TO RITUXIMAB TREATMENT IN PATIENTS WITH ACQUIRED AUTOIMMUNE RECURRENT THROMBOTIC THROMBOCYTOPENIC PURPURA (TTP) | |||||||||||||
Medical condition: THROMBOTIC THROMBOCYTOPENIC PURPURA | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001503-23 | Sponsor Protocol Number: ALX0681-C302 | Start Date*: 2016-08-16 | |||||||||||
Sponsor Name:Ablynx NV | |||||||||||||
Full Title: Prospective Follow-up Study for Patients who Completed Study ALX0681-C301 (HERCULES) to Evaluate Long-term Safety and Efficacy of Caplacizumab (Post-HERCULES) | |||||||||||||
Medical condition: Acquired thrombotic thrombocytopenic purpura (TTP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) ES (Completed) HU (Completed) GB (Completed) CZ (Completed) BE (Completed) FR (Completed) DE (Completed) NL (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019375-30 | Sponsor Protocol Number: ALX-0681-2.1/10 | Start Date*: 2010-09-07 | |||||||||||
Sponsor Name:Ablynx | |||||||||||||
Full Title: A Phase II single blind, randomized, placebo controlled trial to study the efficacy and safety of anti-von Willebrand factor Nanobody administered as adjunctive treatment to patients with acquired ... | |||||||||||||
Medical condition: Acquired thrombotic thrombocytopenic purpura (TTP) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) AT (Completed) GB (Completed) DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001098-42 | Sponsor Protocol Number: ALX0681-C301 | Start Date*: 2015-08-27 | |||||||||||
Sponsor Name:Ablynx NV | |||||||||||||
Full Title: A Phase III double-blind, randomized, parallel group, multicenter placebo-controlled trial to study the efficacy and safety of caplacizumab in patients with acquired thrombotic thrombocytopenic pur... | |||||||||||||
Medical condition: Acquired Thrombotic thrombocytopenic purpura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) ES (Completed) AT (Completed) DE (Completed) HU (Completed) NL (Completed) Outside EU/EEA IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005288-30 | Sponsor Protocol Number: 2019/408/HP | Start Date*: 2020-12-28 | |||||||||||
Sponsor Name:CHU de Rouen | |||||||||||||
Full Title: Efficacy of a personalized caplacizumab regimen based on ADAMTS-13 activity monitoring in adult acquired thrombotic thrombocytopenic purpura: A phase II, multicenter non-inferiority single-arm study | |||||||||||||
Medical condition: acquired thrombotic thrombocytopenic purpura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000249-30 | Sponsor Protocol Number: 15-HMedIdeS-08 | Start Date*: 2016-07-14 | |||||||||||
Sponsor Name:Hansa Medical AB | |||||||||||||
Full Title: A PHASE II PILOT STUDY TO EVALUATE THE SAFETY, TOLERABILITY, EFFICACY, PHARMACODYNAMICS AND PHARMACOKINETICS OF IDES IN ASYMPTOMATIC ANTIBODY-MEDIATED THROMBOTIC THROMBOCYTOPENIC PURPURA (TTP) PATI... | |||||||||||||
Medical condition: Asymptomatic antibody-mediated thrombotic thrombocytopenic purpura (TTP) with low ADAMTS13 activity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003775-35 | Sponsor Protocol Number: SHP655-201 | Start Date*: 2019-07-03 | |||||||||||
Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
Full Title: A Phase 2, multicenter, randomized, placebo-controlled, double-blind study in patients with acquired thrombotic thrombocytopenic purpura (aTTP) to evaluate the pharmacokinetics, safety, and efficac... | |||||||||||||
Medical condition: acquired thrombotic thrombocytopenic purpura (aTTP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004371-19 | Sponsor Protocol Number: ARC1779-004 | Start Date*: 2007-11-20 | ||||||||||||||||
Sponsor Name:Archemix Corp. | ||||||||||||||||||
Full Title: A Phase 2 Pilot Study of the Safety, Pharmacokinetics, and Pharmacodynamics of ARC1779 Injection in Patients with von Willebrand Factor-Related Platelet Function Disorders | ||||||||||||||||||
Medical condition: von Willebrand Factor- related platelet function disorders : thrombotic thrombocytopenic purpura(TTP) in remission, acute TTP, and von Willebrand Disease Type- 2b (vWD-2b). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001117-86 | Sponsor Protocol Number: 16/0340 | Start Date*: 2017-07-25 |
Sponsor Name:University College London | ||
Full Title: A phase IV, prospective, randomised single-blind UK multicentre non-inferiority trial of low-dose versus standard dose rituximab for prevention of relapses in acquired TTP | ||
Medical condition: Acquired thrombotic thrombocytopenic purpura | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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