- Trials with a EudraCT protocol (127)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
127 result(s) found for: Malignant ascites.
Displaying page 6 of 7.
EudraCT Number: 2011-001836-44 | Sponsor Protocol Number: UCL/11/0119 | Start Date*: 2012-06-11 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: A Phase II Trial to Assess the Activity of TroVax® (MVA-5T4) Versus Placebo in Patients with Relapsed Asymptomatic Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer. | |||||||||||||
Medical condition: Patients with relapsed asymptomatic epithelial ovarian, fallopian tube or primary peritoneal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001467-22 | Sponsor Protocol Number: A6181040 | Start Date*: 2004-10-26 |
Sponsor Name:Pfizer S.A. | ||
Full Title: A PHASE 2 EFFICACY AND SAFETY STUDY OF SU011248 IN PATIENTS WITH METASTATIC NON-SMALL CELL LUNG CANCER | ||
Medical condition: Histologically proven NSCLC (Stage IV or recurrent disease or locally advanced [Stage IIIB]) that is not amenable to surgery, radiation, or combined modality therapy with curative intent | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004780-13 | Sponsor Protocol Number: CeNturIOn-2016 | Start Date*: 2018-08-22 | |||||||||||
Sponsor Name:NHS Greater Glasgow & Clyde [...] | |||||||||||||
Full Title: An open-label, randomised, phase II trial of ruCaparib combined with Nivolumab +/- Ipilimumab to augment response in homologous repair deficient patients with relapsed Ovarian, primary peritoneal a... | |||||||||||||
Medical condition: High grade serous ovarian cancer (includes histologically identical fallopian tube and primary peritoneal cancers and high grade G3 endometrioid histological subtypes) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022757-42 | Sponsor Protocol Number: IMM-101-002 | Start Date*: 2011-05-17 | |||||||||||
Sponsor Name:Immodulon Therapeutics Limited | |||||||||||||
Full Title: A Randomised, Open-Label, Proof-of-Concept, Phase II Trial Comparing Gemcitabine with and without IMM-101 in Advanced Pancreatic Cancer | |||||||||||||
Medical condition: Advanced pancreatic cancer The overall objective of this clinical study is to evaluate a potential synergy between gemcitabine and IMM-101 and any beneficial effect this may have on safety and to... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) IT (Completed) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002459-27 | Sponsor Protocol Number: CL1-81694-003 | Start Date*: 2017-12-14 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Phase I/II trial of S 81694 administered intravenously in combination with paclitaxel to evaluate the safety, pharmacokinetic and efficacy in metastatic breast cancer | |||||||||||||
Medical condition: Metastatic Breast Cancer (mBC) and metastatic Triple Negative Breast Cancer (mTNBC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001099-31 | Sponsor Protocol Number: I5B-MC-JGDP | Start Date*: 2017-05-26 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 1b (Open-Label) / Phase 2 (Randomized, Double-Blinded) Study Evaluating Nab-Paclitaxel and Gemcitabine With or Without Olaratumab in the Treatment of First-Line Metastatic Pancreatic Cancer | |||||||||||||
Medical condition: First-Line Metastatic Pancreatic Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005037-37 | Sponsor Protocol Number: 10-005 | Start Date*: 2013-10-02 | |||||||||||||||||||||
Sponsor Name:Puma Biotechnology, Inc. | |||||||||||||||||||||||
Full Title: A Phase I/II Trial of Temsirolimus Plus Neratinib for Patients with Metastatic HER2-Amplified or Triple-Negative Breast Cancer | |||||||||||||||||||||||
Medical condition: advanced breast carcinoma in patients with trastuzumab-refractory HER2-amplified disease | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) ES (Completed) DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001476-33 | Sponsor Protocol Number: CO17/94837 | Start Date*: 2017-09-05 | ||||||||||||||||
Sponsor Name:University of Leeds | ||||||||||||||||||
Full Title: A randomised phase II trial of nivolumab in combination with alternatively scheduled ipilimumab in first-line treatment of patients with advanced or metastatic renal cell carcinoma | ||||||||||||||||||
Medical condition: Previously untreated metastatic clear cell renal cell carcinoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003812-36 | Sponsor Protocol Number: MORAb-003-011 | Start Date*: 2015-06-30 | |||||||||||
Sponsor Name:Morphotek Inc | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-Controlled, Phase 2 Study to Assess the Efficacy and Safety of Farletuzumab (MORAb 003) in Combination with Carboplatin plus Paclitaxel or Carboplatin plus Pegyl... | |||||||||||||
Medical condition: Serious epithelial ovarian cancer including primary peritoneal and fallopian tube malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001426-26 | Sponsor Protocol Number: A8471005 | Start Date*: 2014-04-13 | |||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A phase 2, randomized, open label study to evaluate the efficacy, safety, pharmacodynamics, pharmacokinetics of the anti-ALK-1 MAB PF-03446962 in combination with best supportive care vs. best supp... | |||||||||||||
Medical condition: Advanced hepatocellular carcinoma (HCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004309-24 | Sponsor Protocol Number: A6181112 | Start Date*: 2007-05-02 | |||||||||||
Sponsor Name:Pfizer Inc., East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE IIIB, RANDOMIZED, ACTIVE CONTROLLED OPEN-LABEL STUDY OF SUNITINIB (SUTENT®) 37.5 MG DAILY VS IMATINIB MESYLATE 800 MG DAILY IN THE TREATMENT OF PATIENTS WITH GASTROINTESTINAL STROMAL TUMORS... | |||||||||||||
Medical condition: TREATMENT OF PATIENTS WITH GASTROINTESTINAL STROMAL TUMORS (GIST) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) ES (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005471-24 | Sponsor Protocol Number: GINECO-OV236b | Start Date*: 2016-04-19 | ||||||||||||||||
Sponsor Name:ARCAGY-GINECO | ||||||||||||||||||
Full Title: A randomized, double-blinded, phase III study of atezolizumab versus placebo in patients with late relapse of epithelial ovarian, fallopian tube, or peritoneal cancer treated by platinum-based chem... | ||||||||||||||||||
Medical condition: Patients with late relapse of epithelial ovarien cancer, fallopian tube or peritoneal cancer treated with chemotherapy , bevacizumab and a anti PD-L1 | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Completed) ES (Ongoing) AT (Completed) DE (Completed) BE (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019500-23 | Sponsor Protocol Number: MPD-RC111 | Start Date*: 2012-02-15 | ||||||||||||||||
Sponsor Name:CONSORZIO MARIO NEGRI SUD | ||||||||||||||||||
Full Title: Single Arm Salvage Therapy with Pegylated Interferon Alfa-2a for Patients with High Risk Polycythemia Vera or High Risk Essential Thrombocythemia who are Either Hydroxyurea Resistant or Intolerant ... | ||||||||||||||||||
Medical condition: High risk polycythemia vera and high risk essential thrombocythemia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003680-62 | Sponsor Protocol Number: CHIPPI-1808 | Start Date*: 2019-02-06 | |||||||||||||||||||||
Sponsor Name:Centre Oscar Lambret | |||||||||||||||||||||||
Full Title: Phase III randomized clinical trial evaluating hyperthermic intraperitoneal chemotherapy (HIPEC) in ovarian cancer considering two different settings: Primary Debulking Surgery (PDS) and Interval D... | |||||||||||||||||||||||
Medical condition: Epithelial ovarian cancer, Fallopian tube ovarian cancer, Peritoneal ovarian cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000093-29 | Sponsor Protocol Number: 9785-CL-1121 | Start Date*: 2014-06-02 | |||||||||||||||||||||
Sponsor Name:Astellas Pharma Global Development, Inc. | |||||||||||||||||||||||
Full Title: A Phase 2, Multicenter, Open-label Study to Assess the Efficacy and Safety of Enzalutamide with Trastuzumab in Subjects with HER2+ AR+ Metastatic or Locally Advanced Breast Cancer | |||||||||||||||||||||||
Medical condition: Subjects with HER2+ AR+ Metastatic or Locally Advanced Breast Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-014876-23 | Sponsor Protocol Number: EZN-2208-04 | Start Date*: 2010-05-20 | |||||||||||
Sponsor Name:Enzon Pharmaceuticals, Inc | |||||||||||||
Full Title: A Phase 2 Study of EZN-2208 (PEG-SN38) Administered With or Without Cetuximab in Patients with Metastatic Colorectal Carcinoma (mCRC) | |||||||||||||
Medical condition: mestatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005153-32 | Sponsor Protocol Number: HGS1012-C1072 | Start Date*: 2008-03-26 | |||||||||||
Sponsor Name:Human Genome Sciences Inc. | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, MULTI-CENTER, OPEN-LABEL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF MAPATUMUMAB ( [HGS1012], A FULLY HUMAN MONOCLONAL ANTIBODY TO TRAIL-R1) IN COMBINATION WITH CARBOPLATIN ... | |||||||||||||
Medical condition: Advanced Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007786-23 | Sponsor Protocol Number: A4061046 | Start Date*: 2009-04-23 | |||||||||||
Sponsor Name:Pfizer, S.A. | |||||||||||||
Full Title: ESTUDIO EN FASE 2 ALEATORIZADO Y DOBLE CIEGO DE AXITINIB (AG-013736) CON O SIN AJUSTE DE LA DOSIS EN PACIENTES CON CANCER DE CELULAS RENALES METASTASICO RANDOMIZED, DOUBLE-BLIND PHASE 2 STUDY OF A... | |||||||||||||
Medical condition: CCR metastásico Metastatic RCC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000330-36 | Sponsor Protocol Number: TLK286.3020 | Start Date*: 2004-09-07 |
Sponsor Name:TELIK, INC. | ||
Full Title: Phase 3 Randomized Study of TLK286 versus Gefitinib (Iressa) as Third-Line Therapy in Locally Advanced or Metastatic Non-Small Cell Lung Cancer | ||
Medical condition: Treatment of patients with locally advanced or metastatic non-small cell lung cancer after failure of both platinum-based and docetaxel chemotherapies. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000673-38 | Sponsor Protocol Number: EGF111438 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A Randomized, Multicentre, Open-Label, Phase III Study of Lapatinib plus Capecitabine versus Trastuzumab plus Capecitabine in Patients with Anthracycline- or Taxane-Exposed ErbB2-Positive Metastati... | |||||||||||||
Medical condition: Metastatic breast cancer overexpressing ErbB2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) ES (Prematurely Ended) BE (Prematurely Ended) IT (Prematurely Ended) SE (Completed) DK (Prematurely Ended) HU (Completed) GB (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
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