- Trials with a EudraCT protocol (119)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
119 result(s) found for: Mesothelioma.
Displaying page 4 of 6.
EudraCT Number: 2016-002286-60 | Sponsor Protocol Number: IND.227 | Start Date*: 2019-08-01 | |||||||||||
Sponsor Name:IFCT | |||||||||||||
Full Title: A PHASE II/III RANDOMIZED STUDY OF PEMBROLIZUMAB IN PATIENTS WITH ADVANCED MALIGNANT PLEURAL MESOTHELIOMA | |||||||||||||
Medical condition: ADVANCED MALIGNANT PLEURAL MESOTHELIOMA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005621-24 | Sponsor Protocol Number: N14PLU | Start Date*: 2014-07-17 | ||||||||||||||||
Sponsor Name:Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | ||||||||||||||||||
Full Title: PeRsOnalized treatment fOr patients with pleural eFfusions due to malignant pleural mesothelioma or lung cancer in second or third line. An open label phase II study (Acronym: the PROOF study) | ||||||||||||||||||
Medical condition: Proven pleural effusion of malignant pleural mesothelioma or non small cell lung cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005642-59 | Sponsor Protocol Number: AK-2015-LC-1 | Start Date*: 2016-02-23 | |||||||||||||||||||||
Sponsor Name:Rigshospitalet, Department of Clinical Physiology, Nuclear Medicine and PET | |||||||||||||||||||||||
Full Title: Phase II trial: uPAR-PET for prognostication in patients with non-small cell lung cancer and large cell neuroendocrine carcinoma of the lung | |||||||||||||||||||||||
Medical condition: Non-small cell lung cancer and large cell neuroendocrine carcinoma of the lung | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004420-39 | Sponsor Protocol Number: 05-10 | Start Date*: 2006-05-18 |
Sponsor Name:All-Ireland Co-operative Oncology Research Group (ICORG) | ||
Full Title: An Open Label Phase II Multicentre Clinical Trial of Single Agent VELCADE (Bortezomib) in Patients with Malignant Pleural Mesothelioma | ||
Medical condition: Malignant Pleural Mesothelioma (in first line, and second line treatment settings) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) GB (Completed) BE (Completed) NL (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2012-003650-88 | Sponsor Protocol Number: BAY94-9343/15743 | Start Date*: 2015-11-25 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A randomized, open-label, active-controlled, Phase II study of intravenous anetumab ravtansine (BAY 94-9343) or vinorelbine in patients with advanced or metastatic malignant pleural mesothelioma ov... | |||||||||||||
Medical condition: Patients with advanced or metastatic malignant pleural mesothelioma overexpressing mesothelin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DE (Completed) BE (Completed) GB (Completed) ES (Completed) NL (Completed) PL (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002762-12 | Sponsor Protocol Number: MESOT-TREM-2012 | Start Date*: 2012-06-29 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | ||||||||||||||||||
Full Title: A SECOND-LINE, SINGLE ARM, PHASE II CLINICAL STUDY WITH TREMELIMUMAB, A FULLY HUMANIZED ANTI-CTLA-4 MONOCLONAL ANTIBODY, AS MONOTHERAPY IN PATIENTS WITH UNRESECTABLE MALIGNANT MESOTHELIOMA | ||||||||||||||||||
Medical condition: Patients affected by advanced malignant mesothelioma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001121-24 | Sponsor Protocol Number: P00804 | Start Date*: 2011-04-21 |
Sponsor Name:Papworth Hospital NHS Trust | ||
Full Title: Prospective randomised controlled trial of video assisted thorascopic (VATS) cytoreductive pleurectomy compared to talc pleurodesis in patients with suspected or proven malignant mesothelioma | ||
Medical condition: Mesothelioma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004273-28 | Sponsor Protocol Number: EORTC 08031 | Start Date*: 2005-11-15 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: A phase II feasibility trial of induction chemotherapy followed by extrapleural pneumonectomy and postoperative radiotherapy in patients with malignant pleural mesothelioma. | |||||||||||||
Medical condition: malignant pleural mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001132-36 | Sponsor Protocol Number: GOIRC-03-2016 | Start Date*: 2016-10-03 | |||||||||||
Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA CLINICA (GOIRC) | |||||||||||||
Full Title: A double-blind, placebo controlled, randomized multicenter Phase II Study evaluating Gemcitabine with or without Ramucirumab as II line treatment for advanced malignant pleural mesothelioma | |||||||||||||
Medical condition: diffuse malignant pleural mesethelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000493-15 | Sponsor Protocol Number: NVALT30 | Start Date*: 2020-08-13 | ||||||||||||||||
Sponsor Name:Radboud University Medical Center | ||||||||||||||||||
Full Title: Dose tapering and Early Discontinuation to InCreAse cosT-effectIveness Of immunotherapy for Non-small cell lung carcinoma trial number 1 | ||||||||||||||||||
Medical condition: non-small cell lung cancer | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005535-10 | Sponsor Protocol Number: H3E-MC-JMHX(c) | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:Eli Lilly and Company Limited | |||||||||||||
Full Title: A Phase 2 study of ALIMTA in solid tumor patients with stable third-space fluid | |||||||||||||
Medical condition: either (1) relapsed, advanced (Stage III or IV) NSCLC or (2) malignant pleural or peritoneal mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000521-38 | Sponsor Protocol Number: EORTC-08112 | Start Date*: 2017-06-30 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Nintedanib as maintenance treatment of malignant pleural mesothelioma (NEMO): a double-blind randomized phase II study of the EORTC Lung Cancer Group | |||||||||||||
Medical condition: Malignant pleural mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000061-20 | Sponsor Protocol Number: 20322 | Start Date*: 2019-05-23 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Bayer AG | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: An open-label, multicenter rollover study to provide continued treatment with anetumab ravtansine for participants with solid tumors who were enrolled in previous Bayer-sponsored studies. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) BE (Completed) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001515-23 | Sponsor Protocol Number: PROICM2019-03MES | Start Date*: 2020-01-29 |
Sponsor Name:Institut Régional du Cancer de Montpellier | ||
Full Title: Phase II multicenter randomized trial evaluating the association of PIPAC and systemic chemotherapy versus systemic chemotherapy alone as 1st-line treatment of Malignant Peritoneal Mesothelioma | ||
Medical condition: Patient with Histologically-confirmed diagnosis of peritoneal malignant mesothelioma and non eligible for cytoreductive surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002223-14 | Sponsor Protocol Number: MPM2005 | Start Date*: 2005-08-25 |
Sponsor Name:Rigshospitalet | ||
Full Title: Fase II study of carboplatin and vinorelbine in malignant pleural mesothelioma | ||
Medical condition: Patients with malignant pleural mesothelioma who cannot be operated | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003633-16 | Sponsor Protocol Number: D4200C00075 | Start Date*: 2007-10-11 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A RANDOMIZED PHASE II TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF VANDETANIB (ZD6474, ZACTIMATM) VERSUS VINORELBINE IN PATIENTS WITH INOPERABLE OR RELAPSED MALIGNANT MESOTHELIOMA | ||
Medical condition: Malignant mesothelioma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004592-35 | Sponsor Protocol Number: 6836 | Start Date*: 2010-06-16 |
Sponsor Name:Barts Health NHS Trust | ||
Full Title: A Randomised Stratified Multicentre Phase II Clinical Trial of Single-Agent ADI-PEG 20 (Pegylated Arginine Deiminase) in Patients with Malignant Pleural Mesothelioma. | ||
Medical condition: Mesothelioma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-005033-16 | Sponsor Protocol Number: ASTX295-01 | Start Date*: 2022-12-07 | ||||||||||||||||||||||||||
Sponsor Name:Astex Pharmaceuticals, Inc. | ||||||||||||||||||||||||||||
Full Title: Phase 1/2 Open-Label Study of the Safety, Pharmacokinetics, and Preliminary Activity of ASTX295 in Subjects with Wild-Type TP53 Advanced Solid Tumors | ||||||||||||||||||||||||||||
Medical condition: Subjects with Wild-Type TP53 Advanced Solid Tumors | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) FR (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004388-37 | Sponsor Protocol Number: 69HCL19_0457 | Start Date*: 2020-03-03 | ||||||||||||||||
Sponsor Name:Hospices Civils de Lyon | ||||||||||||||||||
Full Title: A Three-Cohort Phase II trial to Assess the Efficacy of a Maintenance Treatment with TALAzoparib following First Line Platinum-based Chemotherapy in Pleural and Malignant Peritoneal MESOthelioma Pa... | ||||||||||||||||||
Medical condition: This study involves adults subjects with advanced malignant pleural (cohort A) or peritoneal (cohorts B1 and B2) mesothelioma. The cohorts B1 will be patient populations with non-resected or incomp... | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001099-75 | Sponsor Protocol Number: CCRG13-002 | Start Date*: 2015-10-13 | ||||||||||||||||
Sponsor Name:Antwerp University Hospital | ||||||||||||||||||
Full Title: First-line immunotherapy using Wilms’ tumor protein 1 (WT1)-targeted dendritic cell vaccinations for malignant pleural mesothelioma. | ||||||||||||||||||
Medical condition: Treatment-naïve malignant pleural mesothelioma patients (eligible for standard chemotherapy and, in case of resectable disease, surgery) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
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