- Trials with a EudraCT protocol (187)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
187 result(s) found for: Kaplan-Meier method.
Displaying page 5 of 10.
EudraCT Number: 2009-017024-82 | Sponsor Protocol Number: HSJD-EPEP09 | Start Date*: 2012-01-02 | |||||||||||
Sponsor Name:FUNDACIÓN SANT JOAN DE DEU | |||||||||||||
Full Title: Clinical and neuropsychological factors associated with second generation antipsychotic response in patients diagnosed with first episode of early onset schizophrenia spectrum disorders | |||||||||||||
Medical condition: First episode of early onset schizophrenia spectrum disorders | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003835-40 | Sponsor Protocol Number: RG12-024 | Start Date*: 2012-12-10 |
Sponsor Name:University of Birmingham | ||
Full Title: A multicentre, phase II randomised controlled trial evaluating cabazitaxel versus docetaxel re-challenge for the treatment of metastatic Castrate Refractory Prostate Cancer, previously treated with... | ||
Medical condition: Metastatic Castrate Refractory Prostate Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002460-31 | Sponsor Protocol Number: BTI-202 | Start Date*: 2020-10-07 | |||||||||||
Sponsor Name:BioAegis Therapeutics, Inc. | |||||||||||||
Full Title: A PHASE 2 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PROOF-OF-CONCEPT STUDY TO EVALUATE THE EFFICACY AND SAFETY OF RECOMBINANT HUMAN PLASMA GELSOLIN (RHU-PGSN) ADDED TO STANDARD OF CARE FOR TREA... | |||||||||||||
Medical condition: severe COVID-19 pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003321-57 | Sponsor Protocol Number: NHL 2005 XX | Start Date*: 2005-12-23 |
Sponsor Name:UHL NHL Trust | ||
Full Title: Treatment protocol for relapsed anaplastic large cell lymphoma of childhood and adolescence | ||
Medical condition: Anaplastic large cell lymphoma | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004353-24 | Sponsor Protocol Number: LAMVYX | Start Date*: 2019-11-04 | |||||||||||
Sponsor Name:Fundación PETHEMA | |||||||||||||
Full Title: A phase II, multicentre, open label clinical trial to assess the efficacy and toxicity of induction and consolidation with CPX-351 for patients aged 60 to 75 years with secondary or high-risk acute... | |||||||||||||
Medical condition: Newly diagnosed secondary or high risk AML | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001872-13 | Sponsor Protocol Number: PTC299-VIR-015-COV19 | Start Date*: 2021-01-15 | |||||||||||
Sponsor Name:PTC Therapeutics, Inc. | |||||||||||||
Full Title: Evaluation of the efficacy and safety of PTC299 in hospitalized subjects with COVID-19 (FITE19) | |||||||||||||
Medical condition: Coronavirus disease 2019 (COVID-19) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Prematurely Ended) FR (Completed) BE (Completed) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001547-43 | Sponsor Protocol Number: ET19-075 | Start Date*: 2022-01-18 | |||||||||||
Sponsor Name:Centre Léon Bérard | |||||||||||||
Full Title: ATEZOGIST – A prospective, randomized, multicenter, comparative study of the efficacy of imatinib resumption combined with atezolizumab versus imatinib resumption alone in patients with unresectabl... | |||||||||||||
Medical condition: Unresectable locally advanced or metastatic gastrointestinal stromal tumors (GIST) after failure of standard treatments | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005428-81 | Sponsor Protocol Number: P140402 | Start Date*: 2015-07-06 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: A Phase I/II, Open-Label, Multicentre Study to Assess The Safety, Tolerability, Pharmacokinetics and Clinical Efficacy of AZD4547 in Patients with glioma positive for an FGFR fusion Relapsed/Refrac... | |||||||||||||
Medical condition: Recurrent grade III or IV glioma with FGFR3-TACC3 or FGFR1-TACC1 fusion positive by RT-PCR | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003810-15 | Sponsor Protocol Number: PazoDoble | Start Date*: 2013-12-20 | ||||||||||||||||
Sponsor Name:NOGGO e.V. | ||||||||||||||||||
Full Title: Pazopanib versus Pazopanib plus Gemcitabine in patients with relapsed or metastatic uterine leiomyosarcomas or other uterine tumour: a multi-center, randomized phase-II clinical trial of the NOGGO ... | ||||||||||||||||||
Medical condition: This study is a prospective, randomized, open-label, multicenter phase II trial in order to determine progression-free survival of patients with refractory or relapsed metastatic uterine leiomyosar... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004270-22 | Sponsor Protocol Number: TMLI_HSM_001 | Start Date*: 2021-09-06 | |||||||||||
Sponsor Name:IRCCS-A.O.U. SAN MARTINO-IST | |||||||||||||
Full Title: PHASE II STUDY OF TOTAL MARROW AND LYMPHOID IRRADIATION (TMLI) GIVEN IN COMBINATION WITH CYCLOPHOSPHAMIDE AND ETOPOSIDE (VP-16) AS CONDITIONING FOR ALLOGENEIC HEMATOPOIETIC STEM CELL TRANSPLANTATIO... | |||||||||||||
Medical condition: Acute Lymphocytic or Myelogenous Leukemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004758-39 | Sponsor Protocol Number: ESR-18-13485 | Start Date*: 2019-06-12 | |||||||||||
Sponsor Name:AZIENDA UNITÀ SANITARIA LOCALE DELLA ROMAGNA | |||||||||||||
Full Title: A PHASE II STUDY OF CAPECITABINE PLUS CONCOMITANT RADIATION THERAPY FOLLOWED BY DURVALUMAB (MEDI4736) AS PREOPERATIVE TREATMENT IN RECTAL CANCER | |||||||||||||
Medical condition: Locally advanced (T3-4 N0-1) rectal cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006176-39 | Sponsor Protocol Number: GOIM21001 | Start Date*: 2012-07-12 | |||||||||||
Sponsor Name:GOIM GRUPPO ONCOLOGICO MERIDIONALE | |||||||||||||
Full Title: Paclitaxel + Bevacizumab versus doxorubicina liposomiale non pegilata (Myocet), cyclophosfamide e Bevacizumab as the first line treatment in HER-2 negative metastatic breast cancer. Multicenter ran... | |||||||||||||
Medical condition: metastatic breast cancer HER2 negative | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005129-35 | Sponsor Protocol Number: FENET-2016 | Start Date*: 2018-02-22 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA DI FERRARA | |||||||||||||
Full Title: "Peptide Receptor Radionuclide Therapy (PRRT) with somatostatin analogs in tumors over-expressing somatostatin receptors" | |||||||||||||
Medical condition: Tumors over-expressing somatostatin receptors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001701-26 | Sponsor Protocol Number: C-III-001 | Start Date*: 2006-02-23 | |||||||||||
Sponsor Name:CESAR Central European Society for | |||||||||||||
Full Title: First- Line Treatment of Postmenopausal Patients with Endocrine Responsive Metastatic Breast Cancer. A Randomized, Multicenter Study Comparing Letrozole Combined with Standard Chemotherapy Vs Letro... | |||||||||||||
Medical condition: hormone-receptor-positive metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Completed) CZ (Prematurely Ended) HU (Prematurely Ended) SI (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005096-85 | Sponsor Protocol Number: XM22-ONC-40041 | Start Date*: 2015-05-25 | ||||||||||||||||
Sponsor Name:Merckle GmbH | ||||||||||||||||||
Full Title: Safety and Efficacy of LONQUEX® (Lipegfilgrastim) in Comparison to Pegfilgrastim (Neulasta®, Amgen Inc.) and Placebo in Patients with Non-Small-Cell Lung Cancer Receiving First-Line Chemotherapy | ||||||||||||||||||
Medical condition: Advanced squamous or non-squamous non-small-cell lung cancer (NSCLC) Stage IIIB/IV | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) HU (Completed) LV (Completed) PL (Prematurely Ended) GR (Completed) BG (Completed) ES (Completed) HR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003693-33 | Sponsor Protocol Number: CDX011-04 | Start Date*: 2016-01-18 | |||||||||||
Sponsor Name:Celldex Therapeutics, Inc. | |||||||||||||
Full Title: A Randomized Multicenter Pivotal Study of CDX-011 (CR011-vcMMAE) in Patients with Metastatic, GPNMB Over-Expressing, Triple-Negative Breast Cancer | |||||||||||||
Medical condition: Metastatic, GPNMB Over-Expressing, Triple-Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Completed) AT (Prematurely Ended) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004327-13 | Sponsor Protocol Number: H8Y-MC-HBBV | Start Date*: 2012-02-06 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Long-Term Open-Label Safety Study of Pomaglumetad Methionil in Patients with Schizophrenia | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) DE (Completed) ES (Prematurely Ended) BE (Prematurely Ended) AT (Prematurely Ended) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001319-36 | Sponsor Protocol Number: FIERCE-21(B-701-U21) | Start Date*: 2017-08-23 | |||||||||||
Sponsor Name:BioClin Therapeutics, Inc. | |||||||||||||
Full Title: A Dose Escalation, Expansion Study of Vofatamab (B 701) Alone, Plus Docetaxel, or Versus Docetaxel in Subjects with Locally Advanced or Metastatic Urothelial Cell Carcinoma who have Relapsed After,... | |||||||||||||
Medical condition: Treatment of progressed or refractory metastatic UCC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) ES (Prematurely Ended) GB (Prematurely Ended) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004211-42 | Sponsor Protocol Number: POL6326-009 | Start Date*: 2020-03-06 | ||||||||||||||||
Sponsor Name:Polyphor Ltd. | ||||||||||||||||||
Full Title: An International, Phase 3, Multicenter, Randomized, Open-Label Trial Comparing Balixafortide in combination with Eribulin versus Eribulin alone in Patients with HER2 negative, Locally Recurrent or ... | ||||||||||||||||||
Medical condition: Patients with HER2 negative, Locally Recurrent or Metastatic Breast Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Prematurely Ended) GB (GB - no longer in EU/EEA) DE (Prematurely Ended) ES (Prematurely Ended) BE (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004699-16 | Sponsor Protocol Number: KRT-232-117 | Start Date*: 2021-03-15 | |||||||||||||||||||||
Sponsor Name:Kartos Therapeutics, Inc. | |||||||||||||||||||||||
Full Title: An Open-Label, Multicenter, Phase 1b/2 Study of the Safety and Efficacy of KRT-232 Combined with a Tyrosine Kinase Inhibitor (TKI) in Patients with Relapsed or Refractory Ph+ Chronic Myeloid Leukem... | |||||||||||||||||||||||
Medical condition: Phase 1b and Phase 2 Arms A and B: Adults with tumor protein 53 wild type (TP53wt) Philadelphia chromosome positive (Ph+) CML in chronic phase who are refractory or intolerant to ≥ 2 prior TKIs and... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) HU (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
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