- Trials with a EudraCT protocol (835)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
835 result(s) found for: TTP.
Displaying page 1 of 42.
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) |
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: 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: 2005-002274-30 | Sponsor Protocol Number: BRD/05/11 | Start Date*: 2005-12-14 |
Sponsor Name:University College London | ||
Full Title: A Study to assess the safety, efficacy and tolerability of Rituximab(Mabthera) in combination with Plasma Exchange in patients with Acute Thrombotic Thrombocytopenia Purpura. | ||
Medical condition: Thrombotic Thrombocytopenia Purpura | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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: 2012-003221-19 | Sponsor Protocol Number: 281101 | Start Date*: 2012-12-17 | |||||||||||
Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
Full Title: BAX 930 (rADAMTS13) A PHASE 1 PROSPECTIVE, UNCONTROLLED, OPEN-LABEL, MULTICENTER, DOSE-ESCALATION STUDY EVALUATING THE SAFETY AND PHARMACOKINETICS IN HEREDITARY TTP (THROMBOTIC THROMBOCYTOPENIC PU... | |||||||||||||
Medical condition: Subjects diagnosed with hereditary thrombotic thrombocytopenic purpura (TTP) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) GB (Completed) PL (Completed) Outside EU/EEA | |||||||||||||
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: 2017-000858-18 | Sponsor Protocol Number: 281102 | Start Date*: 2017-09-12 | |||||||||||
Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
Full Title: A phase 3, prospective, randomized, controlled, open-label, multicenter, 2-period crossover study with a single arm continuation evaluating the safety and efficacy of BAX 930 (rADAMTS13) in the pro... | |||||||||||||
Medical condition: severe congenital thrombotic thrombocytopenic purpura (cTTP, Upshaw-Schulman Syndrome [USS], hereditary thrombotic thrombocytopenic purpura [hTTP]) | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) AT (Completed) FR (Completed) IT (Completed) PL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
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: 2005-005835-87 | Sponsor Protocol Number: GBG41 | Start Date*: 2006-08-16 |
Sponsor Name:GermanBreastGroup | ||
Full Title: A randomized discontinuation phase II study to determine the efficacy of RAD001 in breast cancer patients with bone metastases | ||
Medical condition: Bone metasatsis, Breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005897-28 | Sponsor Protocol Number: P060801 | Start Date*: 2009-01-06 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Utilisation du rituximab dans le purpura thrombotique thrombocytopénique autoimmun en association aux échanges plasmatiques | |||||||||||||
Medical condition: Purpura Thrombotique Thrombocytopénique autoimmun (PTT). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2020-003348-10 | Sponsor Protocol Number: TAK-755-3002 | Start Date*: 2020-11-17 |
Sponsor Name:Baxalta Innovations GmbH | ||
Full Title: 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 o... | ||
Medical condition: congenital Thrombotic thrombocytopenic purpura (TTP) | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) AT (Trial now transitioned) PL (Trial now transitioned) ES (Trial now transitioned) DE (Trial now transitioned) IT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000338-38 | Sponsor Protocol Number: OSAG 101 – PCS-07 | Start Date*: 2007-07-06 |
Sponsor Name:Oncoscience AG | ||
Full Title: A RANDOMIZED, MULTICENTER, PHASE IIB/IIIA STUDY OF GEMCITABINE AND THE MONOCLONAL ANTIBODY NIMOTUZUMAB (OSAG 101) VERSUS GEMCITABINE AND PLACEBO FOR THE TREAMENT OF CHEMOTHERAPY-NAIVE PATIENTS WITH... | ||
Medical condition: Locally advanced or metastatic pancreatic cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-001177-31 | Sponsor Protocol Number: EFC16521 | Start Date*: 2022-08-29 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
Full Title: An open-label, single-arm, multicenter study to evaluate the efficacy and safety of caplacizumab and immunosuppressive therapy without first line therapeutic plasma exchange in adults with immune-m... | |||||||||||||
Medical condition: Thrombotic Thrombocytopenic Purpura | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) AT (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) ES (Ongoing) CZ (Trial now transitioned) IT (Trial now transitioned) GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2016-001563-36 | Sponsor Protocol Number: CRAD001MIL04T | Start Date*: 2016-05-12 |
Sponsor Name:Novartis Pharmaceuticals | ||
Full Title: A Phase II Study of RAD001 in the Treatment of Patients With Plexiform Neurofibromas (PN) Associated With Neurofibromatosis Type 1 (NF1) | ||
Medical condition: Plexiform Neurofibroma Associated With Neurofibromatosis Type 1 | ||
Disease: | ||
Population Age: Children, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2006-000889-36 | Sponsor Protocol Number: H6Q-MC-S020 | Start Date*: 2006-08-10 |
Sponsor Name:Eli Lilly and Company limited | ||
Full Title: A Double-blind, Randomized, Placebo-controlled Multicentre Phase II Study of Maintenance Enzastaurin Following Whole Brain Radiation Therapy in the Treatment of Brain Metastases from Lung Cancer | ||
Medical condition: brain metastastases of non-small or small cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) SE (Completed) DK (Completed) PL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-001279-19 | Sponsor Protocol Number: SONAS2018 | Start Date*: 2019-08-19 | |||||||||||
Sponsor Name:BURL Concepts, Inc. | |||||||||||||
Full Title: Evaluation of the SONAS® ultrasound device for the assessment of bilateral cerebral perfusion in subjects with acute stroke | |||||||||||||
Medical condition: Acute large vessel occlusion (LVO) stroke (NIHSS score: ≥ 10) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
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