Michigan Mesothelioma Fact Sheet
While mesothelioma is a problem in all states, the specific incident rate for Michigan is 1.1 / 100,000. This is below the average rate of 1.1 / 100,000. Click on the tabs below to find mesothelioma and asbestos research in MI, recent MI mesothelioma-related court cases, mesothelioma specialists in MI and potential asbestos hotspots in Michigan.
Michigan Mesothelioma Info
By clicking on the above tabs, you will find information on mesothelioma specific to the state of Michigan
Michigan Research and Clinical Trials
This is a partial list of scientific or medical grants in your state for research into mesothelioma and related illnesses.
Michigan Doctors and Hospitals
This is a partial list of hospitals and physicians that reportedly treat mesothelioma patients in your state.
Michigan Cases
This is a partial list of relevant court cases on mesothelioma in your state.
Disclaimer: Inclusion on this directory does not constitute endorsement by Cancer Monthly, Inc. All physicians who appear in this section do so based on their own expression of interest in the fields of mesothelioma treatment. Cancer Monthly, Inc. has not verified the competence, professional credentials, business practices or validity of the expressed interests of these physicians. Cancer Monthly makes no recommendation of any physician on this list and makes no suggestion that any such physician will cure or prevent any disease. Those consulting a physician on this list should approach the consultation exactly as they would with any other unknown physician.
This is a partial list of scientific or medical grants in your state for research into mesothelioma and related illnesses.
Michigan Doctors and Hospitals
This is a partial list of hospitals and physicians that reportedly treat mesothelioma patients in your state.
Michigan Cases
This is a partial list of relevant court cases on mesothelioma in your state.
Disclaimer: Inclusion on this directory does not constitute endorsement by Cancer Monthly, Inc. All physicians who appear in this section do so based on their own expression of interest in the fields of mesothelioma treatment. Cancer Monthly, Inc. has not verified the competence, professional credentials, business practices or validity of the expressed interests of these physicians. Cancer Monthly makes no recommendation of any physician on this list and makes no suggestion that any such physician will cure or prevent any disease. Those consulting a physician on this list should approach the consultation exactly as they would with any other unknown physician.
Miller v. Ford Motor Co. (In re Certified Question)
No. 131517, SUPREME COURT OF MICHIGAN, May 10, 2007, Argued, July 25, 2007, Decided, July 25, 2007, Filed
No. 131517, SUPREME COURT OF MICHIGAN, May 10, 2007, Argued, July 25, 2007, Decided, July 25, 2007, Filed
Chapin v. A & L Parts, Inc.
SC: 133410, SUPREME COURT OF MICHIGAN, June 22, 2007, Decided
SC: 133410, SUPREME COURT OF MICHIGAN, June 22, 2007, Decided
Chapin v. A & L Parts, Inc.
SC: 133412, SUPREME COURT OF MICHIGAN, June 22, 2007, Decided
SC: 133412, SUPREME COURT OF MICHIGAN, June 22, 2007, Decided
Chapin v. A & L Parts, Inc.
SC: 133178, SUPREME COURT OF MICHIGAN, June 22, 2007, Decided
SC: 133178, SUPREME COURT OF MICHIGAN, June 22, 2007, Decided
Grand Trunk W. R.R. v. 37th Circuit Court Judge
No. 273411, COURT OF APPEALS OF MICHIGAN, September 11, 2008, Decided
No. 273411, COURT OF APPEALS OF MICHIGAN, September 11, 2008, Decided
Chapin v. A & L Parts, Inc.
No. 257917 , COURT OF APPEALS OF MICHIGAN, January 11, 2007, Submitted , January 30, 2007, Decided
No. 257917 , COURT OF APPEALS OF MICHIGAN, January 11, 2007, Submitted , January 30, 2007, Decided
Creech v. W.A. Foote Mem. Hosp.
No. 237437, No. 237438, No. 237439, No. 237440, No. 237441, No. 237442, No. 237443, No. 237444, No. 237445, No. 237446, COURT OF APPEALS OF MICHIGAN, June 8, 2004, Decided
No. 237437, No. 237438, No. 237439, No. 237440, No. 237441, No. 237442, No. 237443, No. 237444, No. 237445, No. 237446, COURT OF APPEALS OF MICHIGAN, June 8, 2004, Decided
SIGRID BREAK, Personal Representative of the Estate of John Break v. OWENS-CORNING FIBERGLAS CORP.
No. 203289, COURT OF APPEALS OF MICHIGAN, May 7, 1999, Decided
No. 203289, COURT OF APPEALS OF MICHIGAN, May 7, 1999, Decided
Hospitals and Cancer Centers
Barbara Ann Karmanos Cancer Institute
110 East Warren Avenue
Detroit, MI
313.745.8746
McAuley Cancer Care Bldg. Room C139
5301 Huron River Dr.
Ypsilanti, MI
734.712.1000
Barbara Ann Karmanos Cancer Institute
110 East Warren Avenue
Detroit, MI
313.745.8746
McAuley Cancer Care Bldg. Room C139
5301 Huron River Dr.
Ypsilanti, MI
734.712.1000
| City | Site |
|
Connors Creek Power Plant River Rouge Power Plant | |
| Alpena |
Presque Isle Corporation |
| Benton Harbor |
Benton Harbor Atomic Power Plant |
| Brook park |
Ford Motor Company |
| Dearborn |
Cluer Roues Steel Ford Motor Company Universal Zonolite company |
| Detroit |
Austin HS Ice Rink Catholic Chancery Building Chevy Stamping Plant Chrysler Plant Detroit Ball Bearing Edison Steam Ford Motor Company General Motors Gear and Axle Great Lakes Steel National Food Warehouse New York Central Railroad Packard Motor Company Quaker Chemical Roseville Chrysler- Plymouth Selfridge Air Force Base Shatter Proof Glass St John's Hospital St Saclalic School Straugh Brewery Snyder Tool |
| Ecouse |
Great Lakes Steel |
| Farmington |
Affiliated Incinerators, Inc |
| Felch |
Groveland Iron Mines |
| Flint |
Chevrolet Auto Plant Ford Motor Company General Motors GM Engine Plant |
| Gibraltar |
Ford Motor Company |
| Gross Point |
Bon Se Cour Hospital Burns Baptist Church Cottage Hospital |
| Grosse Point |
Pancake House |
| Hamburg |
Ford Motor Company |
| Hamtramck |
Chrysler Plant |
| Haperwoods |
Regina HS |
| Hapeville |
Ford Motor Company |
| Highland Park |
Chrysler Auto Plant Sears Warehouse |
| Iron Mountain |
Veterans Admin Hospital |
| Lake Orion |
St Joe's |
| Marysville |
Consumer Power Gas Plant |
| Milan |
Ford Motor Company |
| Monroe |
Detroit Edison Company Fermi Plant |
| Mount Clemmons |
St Joe's |
| Mt. Clemens |
Ford Paint Plant |
| Mt. Pleasant |
Wirtsmouth AFB |
| Northville |
St Mary's Girl School |
| Petoskey |
Brecheisen Diesel |
| Plum Hollow |
Plum Hollow Golf Course |
| Plymouth |
Plymouth HS |
| Pontiac |
General Motors Pontiac |
| Port Huron |
Prestolite Factory Sulfite Paper Mill |
| Republic |
Republic Iron Plant |
| River Rouge |
Ford Motor Company |
| Saginaw |
General Motors Grey Iron Foundry |
| Saginaw Bay |
Consumer's Power House |
| Sandusky |
Ford Motor Company |
| Schwartz Creek |
Buick Freeman Stamping Plant |
| Southfield |
Robin Towers |
| St. Clair |
Detroit Edison Power Plant |
| Sterling Heights |
Ford Power Plant |
| Tonawanda |
Ford Motor Company |
| Trenton |
St Pius Trenton Channel Plant |
| Troy |
Somerset Mall Apts Troy Holiday Inn |
| Warren |
Udilite Corporation |
Research
Swanson, G Marie. Occupational Cancer Surveillance: New Approaches
Grant: 2R01OH002067-08
Grant: 2R01OH002067-08
Abstract: During the first 6 years of this study, telephone interviews have
been completed with over 17,000 subjects. Lifetime cigarette smoking
histories and occupational histories provide data for assessing workplace
risk for eleven cancer sites: lung and bronchus, urinary bladder, colon,
rectum, stomach, esophagus, mesothelioma, eye, salivary glands, liver,
and melanoma of the skin. A primary objective of this study is to
determine occupational cancer risks among blacks and women. Little is
known about such risks among women or blacks because nearly all research
in this area includes only white men. Other specific aims of this study
include investigation of occupational cancer risks among persons who
never smoked cigarettes; assessing whether cancer occurs at a younger age
than expected in conjunction with occupational risks and determination of
occupational cancer risks wig& predominant local industries, such as
automobile manufacturing, construction, primary ferrous metals
manufacturing, machinery manufacturing, and food processing.
Detailed work histories, tobacco use histories, health history, and
demographics have been obtained by telephone interview. By the end of
the current grant period interviews will be completed with 14,900 cancer
cases and 3,366 population referents. Cancer cases were selected from a
population-based cancer registry; population referents were selected by
random digit dialing.
The proposed renewal is for completion of data analysis. The
long-term objectives of this study are to develop new hypotheses about
occupational cancer risks, provide evidence to support previous
suggestions of occupational cancer risk, and ultimately to prevent
cancers resulting from workplace exposures.
Tags: Cancer Information System, Cancer Risk, Environment Related Neoplasm /cancer, Health Survey, Neoplasm /cancer Epidemiology, Occupational Hazard, Tobacco Abuse Agriculture Worker, Bladder Neoplasm, Caucasian, Esophagus Neoplasm, Eye Neoplasm, Female, Food Processing /preparation, Hospital Personnel, Human Age, Human Mortality, Industrial Medicine, Industry, Liver Neoplasm, Lung Neoplasm, Melanoma, Mesothelioma, Military Personnel, Negroid, Rectum Neoplasm, Salivary Gland Neoplasm, Stomach Neoplasm Adult Human (21+), Human Clinical Subject, Interview, Statistics /biometry
Tags: Cancer Information System, Cancer Risk, Environment Related Neoplasm /cancer, Health Survey, Neoplasm /cancer Epidemiology, Occupational Hazard, Tobacco Abuse Agriculture Worker, Bladder Neoplasm, Caucasian, Esophagus Neoplasm, Eye Neoplasm, Female, Food Processing /preparation, Hospital Personnel, Human Age, Human Mortality, Industrial Medicine, Industry, Liver Neoplasm, Lung Neoplasm, Melanoma, Mesothelioma, Military Personnel, Negroid, Rectum Neoplasm, Salivary Gland Neoplasm, Stomach Neoplasm Adult Human (21+), Human Clinical Subject, Interview, Statistics /biometry
- Followup Grant: 5R01OH002067-09
Bright, Robert K. T Cell Focused Cancer Vaccines In Murine Tumor Models
Grant: 1R29CA077351-01
Grant: 1R29CA077351-01
Abstract: DESCRIPTION: (Applicant's Abstract) One in six people will die of cancer.
the systemic nature, recall ability and exquisite specificity of the immune
system makes immunotherapy an attractive prospect for cancer treatment.
Hepatocellular carcinoma, cervical carcinoma, various leukemias and
lymphomas all have proposed viral etiologies. Viral encoded tumor specific
antigens make viral associated tumors strong candidates for immunotherapy.
Recent studies have described the presence of simian virus 40 (SV40)-like
gene sequences and proteins (specifically the large tumor antigen: SV40
Tag) in human osteosarcomas, glioblastomas, ependymomas and malignant
pleural mesotheliomas (MPM), demonstrating SV40 association with certain
human malignancies. To facilitate the development of human clinical
protocols for the immunotherapy of SV40 associated human malignancies, the
proposed study will employ an SV40 murine tumor system to evaluate the
efficacy of CTL transfer therapies and peptide based vaccines designed to
target an immune response to SV40 Tag expressing tumors in vivo. Briefly,
SV40 Tag specific CTL will be generated by immunization of Balb/c mice with
SV40 Tag gene constructs and the epitope specificity determined by using
selected H-2d restricted synthetic peptides representing potential CTL
epitopes on SV40 Tag. These CTL will be utilized to examine the ability of
adoptively transferred T cells to protect against tumor challenge in
syngeneic mice. Further, selected synthetic peptides will be examined for
the ability to actively induce protective tumor immunity in vivo.
Completion of this study will provide valuable information on the active
induction of tumor destructive immunity involving SV40 Tag-epitope specific
CTL in vivo. Moreover, the information generated using the murine SV40
tumor model will expedite the development of reagents and clinical trials
designed to examine SV40 Tag specific immunotherapies for SV40 associated
human malignancies.
Tags: Cytotoxic T Lymphocyte, Neoplasm /cancer Immunology, Neoplasm /cancer Immunotherapy, Neoplasm /cancer Vaccine, Nonhuman Therapy Evaluation, Simian Virus 40, Tumor Antigen Mhc Class I Antigen, Astrocytoma, Disease Model, Drug Screening /evaluation, Ependymoma, Immunogenetics, Mesothelioma, Neoplastic Cell, Neoplastic Transformation, Osteosarcoma, Synthetic Peptide, Virus Antigen, Virus Genetics, Virus Protein, Virus Related Neoplasm /cancer Active Immunization, Laboratory Mouse
Tags: Cytotoxic T Lymphocyte, Neoplasm /cancer Immunology, Neoplasm /cancer Immunotherapy, Neoplasm /cancer Vaccine, Nonhuman Therapy Evaluation, Simian Virus 40, Tumor Antigen Mhc Class I Antigen, Astrocytoma, Disease Model, Drug Screening /evaluation, Ependymoma, Immunogenetics, Mesothelioma, Neoplastic Cell, Neoplastic Transformation, Osteosarcoma, Synthetic Peptide, Virus Antigen, Virus Genetics, Virus Protein, Virus Related Neoplasm /cancer Active Immunization, Laboratory Mouse
- Followup Grant: 5R29CA077351-02
Flaherty, Lawrence E. Southwest Oncology Group
Grant: 5U10CA014028-24
Grant: 5U10CA014028-24
Abstract: Wayne State University (WSU) has been an active institutional member of
the Southwest Oncology Group for over 20 years. Over these years, our
faculty has played an important role in support of SWOG, by providing
leadership in the administrative and scientific functions of SWOG, and
also by meeting and often exceeding patient accrual goals in a continuous
and consistent manner. Thus, WSU has remained in the first quartile of
institution's performance evaluation conducted by SWOG in each of the
last five years.
The clinical research program in cancer at WSU has been organized along
the lines of multidisciplinary disease oriented sites and in a manner
which resembles the organ committee orientation of SWOG. Thus, our
faculty representation in scientific SWOG committees is constituted by
individuals with expertise and commitment towards those areas of
research. Accordingly, the translation of ideas into SWOG studies as
well as the incorporation of SWOG studies and those of NCI designated
high priority trials into WSU treatment priorities get facilitated.
The SWOG membership in WSU and the diversity of disciplinary involvement
by our faculty has continued to grow over the years. To date, 72 WSU
members are currently serving on 104 committees. Similarly, 51 SWOG
studies list a WSU member as a study chairman or as study coordinator
since the last competing application was submitted.
Dr. Laurence Baker, Co-Principal Investigator of this application, will
continue to provide administrative and scientific assistance to SWOG as
the Associate Chairman of the Group. He will assist the new Principal
Investigator, Dr. Manuel Valdivieso, in maintaining the prominence of WSU
as a SWOG member institution.
Tags: Combination Antineoplastic Therapy, Combination Chemotherapy, Neoplasm /cancer Chemotherapy, Neoplasm /cancer Radiation Therapy, Neoplasm /cancer Surgery Bacillus Calmette Guerin Vaccine, Acute Leukemia, Acute Lymphocytic Leukemia, Acute Myelogenous Leukemia, Antineoplastic, Bladder Neoplasm, Bleomycin, Bone Neoplasm, Breast Neoplasm, Cervix Neoplasm, Cis Platinum Compound, Clinical Trial, Colony Stimulating Factor, Colorectal Neoplasm, Cooperative Study, Cyclophosphamide, Cytosine Arabinoside, Dacarbazine, Doxorubicin, Esophagus Neoplasm, Etoposide, Fluorouracil, Gastrointestinal Neoplasm, Germ Cell Neoplasm, Guanine Analog, Head /neck Neoplasm, Human Therapy Evaluation, Ifosfamide, Interferon Alpha, Interleukin 2, Interleukin 3, Leuprolide, Lung Neoplasm, Lymphoma, Melanoma, Melphalan, Mesothelioma, Metastasis, Mitomycin C, Multiple Myeloma, Nasopharyngeal Neoplasm, Neoplasm /cancer Immunotherapy, Neoplasm /cancer Remission /regression, Nonhodgkin's Lymphoma, Osteosarcoma, Ovary Neoplasm, Pleural Neoplasm, Prednisone, Prostate Neoplasm, Renal Cell Carcinoma, Sarcoma, Squamous Cell Carcinoma, Tamoxifen, Thorax Neoplasm, Transitional Cell Carcinoma, Uterus Neoplasm, Vincristine Flow Cytometry, Human Subject
Tags: Combination Antineoplastic Therapy, Combination Chemotherapy, Neoplasm /cancer Chemotherapy, Neoplasm /cancer Radiation Therapy, Neoplasm /cancer Surgery Bacillus Calmette Guerin Vaccine, Acute Leukemia, Acute Lymphocytic Leukemia, Acute Myelogenous Leukemia, Antineoplastic, Bladder Neoplasm, Bleomycin, Bone Neoplasm, Breast Neoplasm, Cervix Neoplasm, Cis Platinum Compound, Clinical Trial, Colony Stimulating Factor, Colorectal Neoplasm, Cooperative Study, Cyclophosphamide, Cytosine Arabinoside, Dacarbazine, Doxorubicin, Esophagus Neoplasm, Etoposide, Fluorouracil, Gastrointestinal Neoplasm, Germ Cell Neoplasm, Guanine Analog, Head /neck Neoplasm, Human Therapy Evaluation, Ifosfamide, Interferon Alpha, Interleukin 2, Interleukin 3, Leuprolide, Lung Neoplasm, Lymphoma, Melanoma, Melphalan, Mesothelioma, Metastasis, Mitomycin C, Multiple Myeloma, Nasopharyngeal Neoplasm, Neoplasm /cancer Immunotherapy, Neoplasm /cancer Remission /regression, Nonhodgkin's Lymphoma, Osteosarcoma, Ovary Neoplasm, Pleural Neoplasm, Prednisone, Prostate Neoplasm, Renal Cell Carcinoma, Sarcoma, Squamous Cell Carcinoma, Tamoxifen, Thorax Neoplasm, Transitional Cell Carcinoma, Uterus Neoplasm, Vincristine Flow Cytometry, Human Subject
- Followup Grant: 2U10CA014028-20
- Followup Grant: 5U10CA014028-21
- Followup Grant: 5U10CA014028-22
Ganju-krishan, Awtar Modulation Of Doxorubicin Efflux In Human Solid Tumors
Grant: 5R01CA057488-03
Grant: 5R01CA057488-03
Abstract: Drug resistance is a major cause for failure of cancer chemotherapy in
refractory disease. Human solid tumor cells may be intrinsically
resistant or may acquire resistance after chemotherapy. Drug resistance
is multifactorial and efflux plays a major part in resistance to a
variety of natural products used in cancer treatment. Anthracycline,
doxorubicin is an important antibiotic used in treatment of a variety of
human malignancies. Rapid cellular efflux of doxorubicin has been
demonstrated in drug resistant tumor cells. Several relatively non-toxic
drugs have been shown to block efflux in vitro and enhance
chemosensitivity. Verapamil, cyclosporin and trifluoperazine have been
used in vivo with the intent to enhance drug retention and clinical
response of refractory tumors.
Our earlier studies have shown that prochlorperazine is a potent
inhibitor of doxorubicin efflux in human solid tumor cells which are
insensitive to efflux blocking action of verapamil. We have completed a
phase I trial to determine the maximum. tolerated dose of
prochlorperazine in vivo. In cells retrieved from patients on this
protocol, significantly enhanced retention of doxorubicin was
demonstrated and clinical responses were seen in no-small cell lung
cancer and mesotheliomas. In the current project, we proposed to carry
out a phase II study combining administration of doxorubicin followed by
2 hr infusion of prochlorperazine. We will also study markers and
mechanisms of doxorubicin resistance in tumor cells and cell lines
established from patients during the course of therapy on these
protocols. Pharmacokinetic and pharmacological data will be collected to
identify parameters which may correlate with positive response to efflux
blocking.
Tags: Antineoplastic Antibiotic, Combination Chemotherapy, Doxorubicin, Multidrug Resistance, Neoplasm /cancer Chemotherapy P Glycoprotein, Active Transport, Carcinoma, Combination Antineoplastic Therapy, Drug Tolerance, Gene Expression, Mesothelioma, Pharmacokinetics, Prochlorperazine, Small Cell Carcinoma Of Lung Tissue /cell Culture
Tags: Antineoplastic Antibiotic, Combination Chemotherapy, Doxorubicin, Multidrug Resistance, Neoplasm /cancer Chemotherapy P Glycoprotein, Active Transport, Carcinoma, Combination Antineoplastic Therapy, Drug Tolerance, Gene Expression, Mesothelioma, Pharmacokinetics, Prochlorperazine, Small Cell Carcinoma Of Lung Tissue /cell Culture
Reeves, Andrew L. Experimental Asbestos Carcinogenesis
Grant: 2R01OH000323-06
Grant: 2R01OH000323-06
Abstract: There is no text on file for this abstract.
Tags: Respiratory Neoplasms, Lung Neoplasms, Silicates, Asbestos Body Cavities, Pleural Cavity, Body Cavities, Serosa, Neoplastic Transformation, Carcinogenesis, Occupational Health, Occupational Hazards, Optics, Microscopy, Electron*, Respiratory Disorders, Pneumoconiosis, Safety And Occupational Health Study Section Chemistry, Analytical Methods, Spectrometry, Atomic Absorption*, Chemistry, Analytical Methods, Spectrometry, Emission*, Chemistry, Analytical Methods, X-ray Structure Analysis*, Mammals, Lagomorphs*, Mammals, Mice*, Mammals, Rats*, Mammals, Rodents, Gerbils*, Mammals, Rodents, Guinea Pigs*, Mammals, Rodents, Hamsters*
Tags: Respiratory Neoplasms, Lung Neoplasms, Silicates, Asbestos Body Cavities, Pleural Cavity, Body Cavities, Serosa, Neoplastic Transformation, Carcinogenesis, Occupational Health, Occupational Hazards, Optics, Microscopy, Electron*, Respiratory Disorders, Pneumoconiosis, Safety And Occupational Health Study Section Chemistry, Analytical Methods, Spectrometry, Atomic Absorption*, Chemistry, Analytical Methods, Spectrometry, Emission*, Chemistry, Analytical Methods, X-ray Structure Analysis*, Mammals, Lagomorphs*, Mammals, Mice*, Mammals, Rats*, Mammals, Rodents, Gerbils*, Mammals, Rodents, Guinea Pigs*, Mammals, Rodents, Hamsters*
Reeves, Andrew L. Experimental Asbestos Cartiogensis
Grant: 5R01OH000323-07
Grant: 5R01OH000323-07
Abstract: There is no text on file for this abstract.
Tags: Respiratory Neoplasms, Lung Neoplasms, Silicates, Asbestos Body Cavities, Pleural Cavity, Body Cavities, Serosa, Neoplastic Transformation, Carcinogenesis, Occupational Health, Occupational Hazards, Optics, Microscopy, Electron*, Respiratory Disorders, Pneumoconiosis, Safety And Occupational Health Study Section Chemistry, Analytical Methods, Spectrometry, Atomic Absorption*, Chemistry, Analytical Methods, Spectrometry, Emission*, Chemistry, Analytical Methods, X-ray Structure Analysis*, Mammals, Lagomorphs*, Mammals, Mice*, Mammals, Rats*, Mammals, Rodents, Gerbils*, Mammals, Rodents, Guinea Pigs*, Mammals, Rodents, Hamsters*
Tags: Respiratory Neoplasms, Lung Neoplasms, Silicates, Asbestos Body Cavities, Pleural Cavity, Body Cavities, Serosa, Neoplastic Transformation, Carcinogenesis, Occupational Health, Occupational Hazards, Optics, Microscopy, Electron*, Respiratory Disorders, Pneumoconiosis, Safety And Occupational Health Study Section Chemistry, Analytical Methods, Spectrometry, Atomic Absorption*, Chemistry, Analytical Methods, Spectrometry, Emission*, Chemistry, Analytical Methods, X-ray Structure Analysis*, Mammals, Lagomorphs*, Mammals, Mice*, Mammals, Rats*, Mammals, Rodents, Gerbils*, Mammals, Rodents, Guinea Pigs*, Mammals, Rodents, Hamsters*
Clinical Trials
Condition: Malignant Mesothelioma
Intervention: Drug: carboplatin; Drug: gemcitabine hydrochloride; Drug: pemetrexed disodium
More Information
Intervention: Drug: carboplatin; Drug: gemcitabine hydrochloride; Drug: pemetrexed disodium
More Information
Condition: Malignant Mesothelioma
Intervention: Drug: pazopanib hydrochloride; Other: laboratory biomarker analysis
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Intervention: Drug: pazopanib hydrochloride; Other: laboratory biomarker analysis
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Condition: Malignant Mesothelioma
Intervention: Drug: cisplatin; Drug: gemcitabine hydrochloride
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Intervention: Drug: cisplatin; Drug: gemcitabine hydrochloride
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Condition: Malignant Mesothelioma; Pulmonary Complications
Intervention: Genetic: microarray analysis; Genetic: protein expression analysis; Genetic: proteomic profiling; Other: laboratory biomarker analysis
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Intervention: Genetic: microarray analysis; Genetic: protein expression analysis; Genetic: proteomic profiling; Other: laboratory biomarker analysis
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Condition: Malignant Mesothelioma
Intervention: Drug: epirubicin hydrochloride; Drug: gemcitabine hydrochloride
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Intervention: Drug: epirubicin hydrochloride; Drug: gemcitabine hydrochloride
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Condition: Malignant Mesothelioma
Intervention: Drug: doxorubicin hydrochloride; Drug: ranpirnase
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Intervention: Drug: doxorubicin hydrochloride; Drug: ranpirnase
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Condition: Malignant Pleural Mesothelioma; MPM; Solid Tumors
Intervention: Drug: pemetrexed, cisplatin and CBP501; Drug: pemetrexed and cisplatin
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Intervention: Drug: pemetrexed, cisplatin and CBP501; Drug: pemetrexed and cisplatin
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Active, not recruiting Dasatinib in Treating Patients With Previously Treated Malignant Mesothelioma
Condition: Malignant Mesothelioma
Intervention: Drug: dasatinib; Other: immunoenzyme technique; Other: immunohistochemistry staining method; Other: laboratory biomarker analysis
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Intervention: Drug: dasatinib; Other: immunoenzyme technique; Other: immunohistochemistry staining method; Other: laboratory biomarker analysis
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Condition: Malignant Mesothelioma
Intervention: Drug: cediranib maleate; Other: laboratory biomarker analysis
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Intervention: Drug: cediranib maleate; Other: laboratory biomarker analysis
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Condition: Mesothelioma; Lung Cancer
Intervention: Drug: Comparator: Suberoylanilide Hydroxamic Acid (Vorinostat, MK0683); Drug: Comparator: Placebo
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Intervention: Drug: Comparator: Suberoylanilide Hydroxamic Acid (Vorinostat, MK0683); Drug: Comparator: Placebo
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Condition: Malignant Mesothelioma
Intervention: Biological: bevacizumab; Drug: cisplatin; Drug: gemcitabine hydrochloride
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Intervention: Biological: bevacizumab; Drug: cisplatin; Drug: gemcitabine hydrochloride
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