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A Study Comparing Pemetrexed Plus Best Supportive Care Versus Best Supportive Care Alone in the Treatment of Mesothelioma

Condition Mesothelioma Estimated Enrollment: 240 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Allocation: Randomized|Intervention Model: Parallel Assignment|Masking: Open Label|Primary Purpose: Treatment Study ID Numbers: 5362|H3E-MC-JMEW Study First Received: September 12, 2005 Last Updated: January 24, 2007 Estimated Primary Completion Date: null Primary Outcome Measures: The primary objective of this study is to compare the overall survival following treatment with Pemetrexed plus best supportive care versus best supportive care alone|To characterize and compare the toxicities of Pemetrexed/best supportive care and best supportive care alone in this patient population;to determine the objective-tumor response rate|to compare time to event efficacy variables of both arms including:duration...

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Bortezomib in Treating Patients With Malignant Pleural Mesothelioma

Condition Malignant Mesothelioma Estimated Enrollment: 33 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Allocation: Non-Randomized|Intervention Model: Single Group Assignment|Masking: Open Label|Primary Purpose: Treatment Study ID Numbers: 05-10 ICORG|ICORG-05-10|EUDRACT-2005-004420-39|EU-20748 Study First Received: August 8, 2007 Last Updated: December 30, 2014 Estimated Primary Completion Date: December 2009 Primary Outcome Measures: Objective tumor response rate (complete response or partial response) as assessed by modified RECIST criteria|Time to disease progression|Overall survival|Safety|Quality of life Sponsors and Collaborators: Cancer Trials Ireland Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT00513877...

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S9810: Gemcitabine Plus Cisplatin in Treating Patients With Malignant Mesothelioma of the Pleura That Cannot Be Removed by Surgery

Condition Malignant Mesothelioma Estimated Enrollment: 57 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Intervention Model: Single Group Assignment|Masking: Open Label|Primary Purpose: Treatment Study ID Numbers: CDR0000066832|SWOG-S9810|U10CA032102 Study First Received: November 1, 1999 Last Updated: October 5, 2012 Estimated Primary Completion Date: June 2007 Primary Outcome Measures: Estimate overall survival|qualitative and quantitative toxicities|confirmed and unconfirmed complete and partial response Sponsors and Collaborators: Southwest Oncology Group|National Cancer Institute (NCI) Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT00003723...

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PTK787/ZK 222584 in Treating Patients With Unresectable Malignant Mesothelioma

Condition Malignant Mesothelioma Estimated Enrollment: 47 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Intervention Model: Single Group Assignment|Masking: Open Label|Primary Purpose: Treatment Study ID Numbers: CALGB-30107|U10CA031946|CDR0000269537 Study First Received: February 5, 2003 Last Updated: June 30, 2016 Estimated Primary Completion Date: July 2005 Primary Outcome Measures: Survival|Failure free survival Sponsors and Collaborators: Alliance for Clinical Trials in Oncology|National Cancer Institute (NCI) Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT00053885...

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Combination Chemotherapy Before Surgery in Treating Patients With Mesothelioma of the Lung

Condition Malignant Mesothelioma Estimated Enrollment: 61 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Intervention Model: Single Group Assignment|Masking: Open Label|Primary Purpose: Treatment Study ID Numbers: SAKK 17/00|SWS-SAKK-17-00|EU-20136 Study First Received: February 14, 2002 Last Updated: May 14, 2012 Estimated Primary Completion Date: May 2003 Primary Outcome Measures: Sponsors and Collaborators: Swiss Group for Clinical Cancer Research Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT00030745...

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SS1(dsFV)PE38 Plus Pemetrexed and Cisplatin to Treat Malignant Pleural Mesothelioma

Condition Mesothelioma Estimated Enrollment: 24 Age Group: 18 Years to 100 Years   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Allocation: Non-Randomized|Intervention Model: Parallel Assignment|Primary Purpose: Treatment Study ID Numbers: 080026|08-C-0026 Study First Received: September 30, 2011 Last Updated: April 20, 2017 Estimated Primary Completion Date: January 31, 2014 Primary Outcome Measures: Safety and MTD|Best overall response Sponsors and Collaborators: National Cancer Institute (NCI)|National Institutes of Health Clinical Center (CC) Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT01445392...

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Bortezomib and Cisplatin as First-Line Therapy in Treating Patients With Malignant Mesothelioma

Condition Malignant Mesothelioma Estimated Enrollment: 82 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Intervention Model: Single Group Assignment|Masking: Open Label|Primary Purpose: Treatment Study ID Numbers: EORTC-08052|JJPRD-26866138CAN2012|2006-000009-51 Study First Received: April 9, 2007 Last Updated: April 19, 2013 Estimated Primary Completion Date: April 2010 Primary Outcome Measures: Progression-free survival (PFS) rate at 18 weeks|Overall objective response rate|Symptomatic response rate|Safety as measured by NCI CTCAE v3.0 and the Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity questionnaire|Duration of PFS|Overall survival Sponsors and Collaborators: European Organisation for Research and Treatment of Cancer - EORTC Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT00458913...

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Surgery and Photodynamic Therapy in Treating Patients With Malignant Mesothelioma

Condition Malignant Mesothelioma Estimated Enrollment: 12 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Intervention Model: Single Group Assignment|Masking: Open Label|Primary Purpose: Treatment Study ID Numbers: CDR0000269674|RPCI-RP-9812 Study First Received: February 5, 2003 Last Updated: February 25, 2011 Estimated Primary Completion Date: June 2006 Primary Outcome Measures: Feasibility|Comparison of results from this regimen to historical controls|Toxic effects Sponsors and Collaborators: Roswell Park Cancer Institute Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT00054002...

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Study of NGR-hTNF as Single Agent in Patients Affected by Advanced or Metastatic Malignant Pleural Mesothelioma

Condition Malignant Pleural Mesothelioma Estimated Enrollment: 57 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Intervention Model: Single Group Assignment|Masking: Open Label|Primary Purpose: Treatment Study ID Numbers: NGR010|EUDRACT Number: 2006-005993-39 Study First Received: June 7, 2007 Last Updated: October 26, 2015 Estimated Primary Completion Date: September 2010 Primary Outcome Measures: • Antitumor activity defined as progression free survival (PFS)|• Tumor Growth Control Rate (TGCR) according to RECIST criteria • Overall survival (OS)|• Experimental Imaging Study (DCE-MRI)|• Pharmacokinetics in patients treated with weekly schedule|•Safety Sponsors and Collaborators: MolMed S.p.A. Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT00484276...

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Extrapleural Pneumonectomy /Pleurectomy Decortication, IHOC Cisplatin and Gemcitabine With Amifostine and Sodium Thiosulfate Cytoprotection for Resectable Malignant Pleural Mesothelioma

Condition Malignant Pleural Mesothelioma Estimated Enrollment: 141 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Allocation: Non-Randomized|Intervention Model: Single Group Assignment|Masking: No masking|Primary Purpose: Treatment Study ID Numbers: 07-091 Study First Received: December 10, 2007 Last Updated: January 19, 2017 Estimated Primary Completion Date: November 2011 Primary Outcome Measures: To establish the maximally tolerated dose (MTD) of intraoperative Intrathoracic/Intraperitoneal hyperthermic gemcitabine and cisplatin combination modulated by amifostine and sodium thiosulfate in patients with malignant pleural mesothelioma.|To determine and quantitate the safety of this combination in these patients by defining the dose limiting toxicity.|To study the pharmacokinetics of gemcitabine and cisplatin combination administered in...

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