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Erlotinib in Treating Patients With Solid Tumors and Liver or Kidney Dysfunction

Condition Adult Anaplastic Astrocytoma|Adult Anaplastic Ependymoma|Adult Anaplastic Oligodendroglioma|Adult Brain Stem Glioma|Adult Diffuse Astrocytoma|Adult Ependymoblastoma|Adult Giant Cell Glioblastoma|Adult Glioblastoma|Adult Gliosarcoma|Adult Mixed Glioma|Adult Myxopapillary Ependymoma|Adult Oligodendroglioma|Adult Pilocytic Astrocytoma|Adult Primary Hepatocellular Carcinoma|Adult Subependymoma|Advanced Adult Primary Liver Cancer|Advanced Malignant Mesothelioma|Male Breast Cancer|Recurrent Adenoid Cystic Carcinoma of the Oral Cavity|Recurrent Adult Brain Tumor|Recurrent Adult Primary Liver Cancer|Recurrent Anal Cancer|Recurrent Basal Cell Carcinoma of the Lip|Recurrent Bladder Cancer|Recurrent Breast Cancer|Recurrent Cervical Cancer|Recurrent Colon Cancer|Recurrent Esophageal Cancer|Recurrent Esthesioneuroblastoma of the Paranasal Sinus and Nasal Cavity|Recurrent Inverted Papilloma of the Paranasal Sinus and Nasal Cavity|Recurrent Lymphoepithelioma of the Nasopharynx|Recurrent Lymphoepithelioma of the Oropharynx|Recurrent Malignant Mesothelioma|Recurrent Metastatic Squamous Neck Cancer...

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Safety and Immune Response to a Multi-component Immune Based Therapy (MKC1106-PP) for Patients With Advanced Cancer.

Condition Ovarian|Melanoma|Renal|Prostate|Colorectal|Endometrial Carcinoma|Cervical Carcinoma|Testicular Cancer|Thyroid Cancer|Small Cell Lung Carcinoma|Mesothelioma|Breast Carcinoma|Esophageal Carcinoma|Gastric Cancer|Pancreatic Carcinoma|Neuroendocrine Cancer|Liver Cancer|Gallbladder Cancer|Biliary Tract Cancer|Anal Carcinoma|Bone Sarcomas|Soft Tissue Sarcomas|Carcinoma of Unknown Origin, Primary Estimated Enrollment: 12 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Allocation: Randomized|Intervention Model: Single Group Assignment|Masking: Open Label|Primary Purpose: Treatment Study ID Numbers: MKC1106-PP-001 Study First Received: January 12, 2007 Last Updated: August 2, 2010 Estimated Primary Completion Date: September 2009 Primary Outcome Measures: To determine the immunologic response to the treatment with MKC1106-PP regimen and 2) to determine the safety and adverse event profile of MKC1106-PP|to determine the blood plasmid levels by PCR analysis|measure cytokine...

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B-Receptor Signaling in Cardiomyopathy

Condition Carcinomas|Amyloidosis|Anal Cancer|Anemia|Cholangiocarcinoma of the Extrahepatic Bile Duct|Transitional Cell Carcinoma of Bladder|Bone Marrow Transplant Failure|Bone Cancer|Cancer of Brain and Nervous System|Breast Cancer|Carcinoma of the Large Intestine|Endocrine Cancer|Esophageal Cancer|Eye Cancer|Gall Bladder Cancer|Gastric (Stomach) Cancer|Gastrooesophageal Cancer|Gastrointestinal Stromal Tumor (GIST)|Gynecologic Cancers|Head and Neck Cancers|Hepatobiliary Neoplasm|Kidney (Renal Cell) Cancer|Leukemia|Lung Cancer|Hodgkin Disease|Lymphoma, Non-Hodgkin|Mesothelioma|Multiple Myeloma|Myelodysplastic Syndromes (MDS)|Neuroendocrine Tumors|Myeloproliferative Disorders|Pancreatic Cancer|Prostate Cancer|Skin Cancer|Soft Tissue Sarcoma|Testicular Cancer|Thymus Cancer|Thyroid Cancer Estimated Enrollment: 99 Age Group: up to 40 Years   (Child, Adult) Gender: All Study Type: Observational Study Design Allocation: Observational Model: Cohort|Time Perspective: Prospective Study ID Numbers: PEDSVAR0038|SU-11172008-1345 Study First Received: June 1, 2010 Last Updated: November 16, 2015 Estimated Primary Completion Date: October 2010 Primary Outcome Measures: Development of...

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Collecting Tumor Samples From Patients With Gynecological Tumors

Condition Borderline Ovarian Clear Cell Tumor|Borderline Ovarian Serous Tumor|Cervical Adenocarcinoma|Cervical Adenosquamous Carcinoma|Cervical Small Cell Carcinoma|Cervical Squamous Cell Carcinoma, Not Otherwise Specified|Childhood Embryonal Rhabdomyosarcoma|Childhood Malignant Ovarian Germ Cell Tumor|Endometrioid Stromal Sarcoma|Gestational Trophoblastic Tumor|Malignant Mesothelioma|Malignant Ovarian Epithelial Tumor|Melanoma|Neoplasm of Uncertain Malignant Potential|Ovarian Brenner Tumor|Ovarian Clear Cell Cystadenocarcinoma|Ovarian Serous Cystadenocarcinoma|Paget Disease of the Vulva|Recurrent Cervical Carcinoma|Recurrent Fallopian Tube Carcinoma|Recurrent Ovarian Carcinoma|Recurrent Ovarian Germ Cell Tumor|Recurrent Primary Peritoneal Carcinoma|Recurrent Uterine Corpus Carcinoma|Recurrent Vaginal Carcinoma|Recurrent Vulvar Carcinoma|Stage I Ovarian Cancer|Stage I Uterine Corpus Cancer|Stage I Vaginal Cancer|Stage I Vulvar Cancer|Stage IA Cervical Cancer|Stage IA Fallopian Tube Cancer|Stage IA Ovarian Cancer|Stage IA Ovarian Germ Cell Tumor|Stage IB...

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Interleukin-12 in Treating Patients With Cancer in the Abdomen

Condition Anal Cancer|Colorectal Cancer|Gallbladder Cancer|Gastric Cancer|Pancreatic Cancer Estimated Enrollment: 29 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: ID97-027|P30CA016672|MDA-ID-97027|NCI-T97-0034|CDR0000065681 Study First Received: November 1, 1999 Last Updated: July 27, 2012 Estimated Primary Completion Date: October 2001 Primary Outcome Measures: Maximum Tolerated Dose (MTD) of Intraperitoneal Interleukin-12 Sponsors and Collaborators: M.D. Anderson Cancer Center|National Cancer Institute (NCI) Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT00003046...

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Study of Previously Collected and Stored Tissue Samples From Patients Previously Enrolled in a Completed National Cancer Institute Clinical Trial

Condition Cancer Estimated Enrollment: 241 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Observational Study Design Allocation: Study ID Numbers: CDR0000573913|NCI-08-C-N013|P07268 Study First Received: May 16, 2009 Last Updated: February 16, 2012 Estimated Primary Completion Date: October 2007 Primary Outcome Measures: Analyses of stored human samples, specimens, and data collected from patients previously enrolled in a terminated National Cancer Institute-Institutional Review Board clinical trial|Correlation of plasma levels and pharmacokinetics with disease burden and presence of antibodies|Correlation of tumor markers with disease burden|Utility of tumor markers for following patients after treatment Sponsors and Collaborators: National Institutes of Health Clinical Center (CC)|National Cancer Institute (NCI) Result Received: No Study Results Posted Website...

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Fentanyl Sublingual Spray in Treating Patients With Breakthrough Cancer Pain

Condition Cancer Estimated Enrollment: 130 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Intervention Model: Crossover Assignment|Masking: Double Blind (Participant, Investigator, Outcomes Assessor)|Primary Purpose: Treatment Study ID Numbers: INS-05-001|CDR0000581128 Study First Received: October 1, 2007 Last Updated: January 14, 2014 Estimated Primary Completion Date: February 2010 Primary Outcome Measures: Summed Pain Intensity Differences (SPID) at 30 Minutes After Dosing (SPID30)|Summed Pain Intensity Differences (SPID) at 5, 10, 15, 45, and 60 Minutes After Dosing|Total Pain Relief (TOTPAR) at 5, 10, 15, 30, 45, and 60 Minutes After Dosing|Global Evaluation of the Study Medication at 30 and 60 Minutes After Dosing Sponsors and Collaborators: INSYS Therapeutics...

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Cyclophosphamide Plus Vaccine Therapy in Treating Patients With Advanced Cancer

Condition Breast Cancer|Colorectal Cancer|Kidney Cancer|Lung Cancer|Malignant Mesothelioma|Pancreatic Cancer Estimated Enrollment: 40 Age Group: 18 Years and older   (Adult, Senior) Gender: All Study Type: Interventional Study Design Allocation: Primary Purpose: Treatment Study ID Numbers: SVMC-ONC-222|CDR0000076913|NCI-V91-0075 Study First Received: November 1, 1999 Last Updated: July 9, 2013 Estimated Primary Completion Date: December 2007 Primary Outcome Measures: Clinical response (patients with evaluable disease)|Duration of response (patients with evaluable disease)|Survival (patients with evaluable disease)|Time to recurrence (patients without evaluable disease)|Survival (patients without evaluable disease) Sponsors and Collaborators: St. Vincent Medical Center - Los Angeles|National Cancer Institute (NCI) Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT00002475...

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Sorafenib, Pemetrexed, and Cisplatin in Treating Patients With Advanced Solid Tumors

Condition Breast Cancer|Colorectal Cancer|Head and Neck Cancer|Lung Cancer|Mesothelioma|Pancreatic Cancer|Prostate Cancer|Sarcoma Estimated Enrollment: 16 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: 2007LS086|0712M22703 Study First Received: June 20, 2008 Last Updated: November 6, 2012 Estimated Primary Completion Date: September 2010 Primary Outcome Measures: Maximum tolerated dose of sorafenib tosylate|Disease Response|Maximum, Minimum and AUC Concentrations of Sorafenib Sponsors and Collaborators: Masonic Cancer Center, University of Minnesota Result Received: No Study Results Posted Website Link: https://ClinicalTrials.gov/show/NCT00703638...

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Quality of Life and Survivorship Care in Patients Undergoing Hyperthermic Intraperitoneal Chemotherapy (HIPEC)

Condition Advanced Malignant Mesothelioma|Carcinoma of the Appendix|Ovarian Sarcoma|Ovarian Stromal Cancer|Pseudomyxoma Peritonei|Recurrent Colon Cancer|Recurrent Malignant Mesothelioma|Recurrent Ovarian Epithelial Cancer|Recurrent Ovarian Germ Cell Tumor|Stage III Colon Cancer|Stage III Ovarian Epithelial Cancer|Stage III Ovarian Germ Cell Tumor|Stage IV Colon Cancer|Stage IV Ovarian Epithelial Cancer|Stage IV Ovarian Germ Cell Tumor|Unspecified Childhood Solid Tumor, Protocol Specific Estimated Enrollment: 10 Age Group: Child, Adult, Senior Gender: All Study Type: Interventional Study Design Allocation: Intervention Model: Single Group Assignment|Masking: Open Label|Primary Purpose: Supportive Care Study ID Numbers: CCCWFU 97110|NCI-2010-00980 Study First Received: May 13, 2010 Last Updated: January 17, 2017 Estimated Primary Completion Date: April 2011 Primary Outcome Measures: Assess feasibility of instituting an orientation program, brief follow up...

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