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Mesothelioma Resource Center: Mesothelioma Ongoing Clinical Trials - Phase 1

Mesothelioma Ongoing Clinical Trials - Phase I


Phase I Study of Optical Coherence Tomography of the Airway of Patients Undergoing Pneumonectomy or Lobectomy for Malignant or Benign Lung Processes

Phase I

Location:

Cleveland, OH: Case Comprehensive Cancer Center

Trial Summary:

Correlate optical coherence tomography images of the airway with airway histology. Develop an imaging technique to detect premalignant airway epithelial changes (carcinoma in situ, dysplasia) to study the transformation process as well as intervene and prevent the development of lung cancer.

Contact Information:
Jeffrey Kern, MD, Principal investigator:
Ph: 216-844-8101; 800-641-2422

Clinical Trials Office - Case Comprehensive Cancer Center:
Ph: 800-641-2422

For Additional Information,  Click Here


Dasatinib in Resectable Malignant Pleural Mesothelioma

Phase I

Location:

Houston, TX: M. D. Anderson Cancer Center at University of Texas

Trial Summary:

The primary objective of this novel Phase I trial will be the level of biomarker modulation of p-Src Tyr 419 by induction dasatinib therapy in patients with resectable malignant pleural mesothelioma.

Contact Information:
Anne S. Tsao, MD Principal Investigator:
Ph: 713-792-6363

James Gil, RN:
Ph: 713-745-6766

For Additional Information,  Click Here


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

Phase I

Location:

Boston, MA: Dana-Farber/Brigham and Women's Cancer Center

Trial Summary:

This is a Phase I trial to study the efficacy of combination chemotherapy consisting of gemcitabine and cisplatin administered in the operating room and put into the chest and abdomen for one hour. Also being looked at are the effects of heating the chemotherapy to a temperature of 42 degrees Celsius and the effect of cytoprotection agents: amifostine and sodium thiosulfate to counteract potential side effects of chemotherapy.

Contact Information:
David J. Sugarbaker, Principal Investigator:
Ph: 617-732-5004
Email: dsugarbaker@partners.org

Tamara Tilleman, M.D, PhD:
Ph: 617-732-5079
Email: ttilleman@partners.org

For Additional Information,  Click Here


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

Phase I

Location:

Minneapolis, MN: Masonic Cancer Center at University of Minnesota

Trial Summary:

Sorafenib and Pemetrexed may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Sorafenib may also stop the growth of tumor cells by blocking blood flow to the tumor. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving sorafenib together with pemetrexed and cisplatin may kill more tumor cells.

Contact Information:
Priya Kumar, MD, Principal investigator:
Ph: 612-625-7667; 888-226-2376

Clinical Trials Office - Masonic Cancer Center at University of Minnesota:
Ph: 612-624-2620

For Additional Information,  Click Here


Phase I Dose-Escalation Study of Azacitidine In Combination With Temozolomide

Phase I

Location:

New York, NY: Herbert Irving Comprehensive Cancer Center at Columbia University Medical Center

Trial Summary:

The purpose of this study is to determine safety and toxicity for the combination of Temozolomide and Azacitidine in the treatment of Advanced Soft Tissue Sarcoma or Malignant Mesothelioma. This is a single-center, open-label, single-arm Phase I dose-escalation trial. Patients will be evaluated with complete history and physical as well as laboratory studies (complete blood count, metabolic panel, liver function tests), biopsy, and imaging of all sites of measurable disease. This study will be conducted over the course of 3 years.

Contact Information:
Robert N. Taub, Principal Investigator
Lilian Batista, BS:
Ph: 212-305-6837
Email: lb2327@columbia.edu

Pamela Pujols, BS:
Ph: 212-305-1923
Email: pp2263@columbia.edu

For Additional Information,  Click Here


Study of Safety and Tolerability of Intravenous CRS-207 in Adults With Selected Advanced Solid Tumors Who Have Failed or Who Are Not Candidates for Standard Treatment

Phase I

Location:

Baltimore, MD: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Philadelphia, PA: Abramson Cancer Center of the University of Pennsylvania

Dallas, TX: Mary Crowley Medical Research Center at Sammons Cancer Center

Trial Summary:

This clinical trial will evaluate the safety and tolerability of CRS 207 an investigational product that is a weakened form (attenuated) of Listeria monocytogenes, a type of bacteria that is commonly found in the environment. CRS-207 has been altered in the lab to reduce its ability to cause disease, while maintaining stimulation of the immune system. CRS 207 has also been genetically modified with recombinant DNA to release an antigen called Mesothelin. Because CRS 207 stimulates an immune response to Mesothelin and Mesothelin may be present at higher levels on tumor cells than on normal cells, this clinical trial will also examine if CRS 207 boosts the immune system in a way that targets certain types of cancer.

Contact Information:
MD: Alice Pons:
Ph: 410-502-9380
Email: ponsal@jhmi.edu
Dung Le, MD, Principal Investigator

PA: Adri Recio, RN:
Ph: 215-573-6760
Email: arecio@mail.med.upenn.edu
Daniel H. Sterman, Principal Investigator

TX: Joyce Bolluyt, RN, CRC:
Ph: 214-658-1943
Email: jbolluyt@marycrowley.org

JR Doan:
Ph: 214-658-1943
Email: jdoan@marycrowley.org
John J. Nemunaitis, Principal Investigator

For Additional Information,  Click Here


Immunotoxin Therapy, Pemetrexed, and Cisplatin in Treating Patients with Malignant Pleural Mesothelioma That Cannot Be Removed by Surgery

Phase I

Location:

Bethesda, MD: Warren Grant Magnuson Clinical Center

Trial Summary:

This Phase I trial is studying the side effects and best dose of immunotoxin therapy when given together with pemetrexed and cisplatin in treating patients with malignant pleural mesothelioma that cannot be removed by surgery.

Contact Information:
Raffit Hassan, MD, Principal investigator:
Ph: 301-451-8742

Clinical Trials Office - Warren Grant Magnusen Clinical Center - NCI Clinical Trials Referral Office:
Ph: 888-NCI-1937

For Additional Information,  Click Here


Pharmacokinetic, Safety, and Efficacy Effects of Oral LBH589 on Dextromethorphan in Patients with Advanced or Metastatic Non-Small Cell Lung Cancer or Malignant Pleural Mesothelioma

Phase I

Location:

Chicago, IL: Rush Cancer Institute at Rush University Medical Center

Houston, TX: M. D. Anderson Cancer Center at University of Texas

Trial Summary:

This study will investigate the effect of oral LBH589 on dextromethorphan, a CYP2D6 substrate, and to assess safety and efficacy of oral LBH589 when used with this co-medication in advanced stage NSCLC or malignant pleural mesothelioma patients.

Contact Information:
Novartis Study Chair U.S:
Ph: 800 340 6843

IL: Robert Bonomi, M.D.
TX: Vali Papa, M.D.

For Additional Information,  Click Here


A Study to Find the Best Dose of SU011248 When Given With Pemetrexed, Pemetrexed and Cisplatin Or Pemetrexed and Carboplatin in Patients With Advanced Solid Tumors

Phase I

Location:

Denver & Aurora, CO: Pfizer Investigational Site

Trial Summary:

This study will assess the maximum tolerated dose, overall safety and antitumor activity of SU011248 in combination with pemetrexed, pemetrexed and cisplatin or pemetrexed and carboplatin in patients with advanced solid tumors.

Contact Information:
Pfizer CT.gov Call Center Study Director
Pfizer Oncology Clinical Trial Information Service:
Ph: 1-877-369-9753
Email: PfizerCancerTrials@emergingmed.com

For Additional Information,  Click Here


Oxaliplatin and Paclitaxel Plus Bevacizumab in Advanced Peritoneal Carcinomatosis

Phase I

Location:

Houston, TX: M. D. Anderson Cancer Center at University of Texas

Trial Summary:

Primary Objectives:
1. To establish acceptable dosages of paclitaxel, oxaliplatin and bevacizumab
2. To assess toxicity profile.
3. To assess clinical responses.

Contact Information:
Siqing Fu, MD, PhD Principal Investigator:
Ph: 713-792-7960

For Additional Information,  Click Here


Phase I Study Using Sunitinib Plus Radiation Therapy for Cancer Patients

Phase I

Location:

Philadelphia, PA: Kimmel Cancer Center at Thomas Jefferson University - Philadelphia

Trial Summary:

This study is using the combination of radiation and antiangiogenic agents (agents that destroy existing blood vessels) which seems to be an approach to tumor cure.

Contact Information:
Adam P Dicker, MD, Ph Principal Investigator:
Ph: 215-955-6527
Email: adam.dicker@jeffersonhospital.org

Alvaro Pereria-Rico, MD:
Ph: 215-955-8874
Email: alvaro.pereria-rico@jefferson.edu

For Additional Information,  Click Here


Cisplatin, Imatinib Mesylate, and Pemetrexed in Malignant Mesothelioma Patients

Phase I

Location:

Houston, TX: M. D. Anderson Cancer Center at University of Texas

Trial Summary:

Primary Objective:
1. To determine the maximum tolerated dose of the combination of cisplatin, imatinib mesylate, and pemetrexed in metastatic malignant mesothelioma.

Contact Information:
Anne S. Tsao, MD Principal Investigator:
Ph: 713-792-6363

For Additional Information,  Click Here


Vaccine Therapy and GM-CSF in Treating Patients With Acute Myeloid Leukemia, Myelodysplastic Syndromes, Non-Small Cell Lung Cancer, or Mesothelioma

Phase I

Location:

New York, NY: Memorial Sloan-Kettering Cancer Center

Trial Summary:

Vaccines made from peptides may help the body build an effective immune response to kill cancer cells. Biological therapies, such as GM-CSF, may stimulate the immune system in different ways and stop cancer cells from growing.

Contact Information:
Lee Krug, MD, Principal investigator:
Ph: 212-639-8420;   800-525-2225

For Additional Information,  Click Here


A Phase I Study of BMS-690514 in Patients with Advanced or Metastatic Solid Tumors

Phase I

Location:

Indianapolis, IN: Indiana University Melvin and Bren Simon Cancer Center;

Houston, TX: M. D. Anderson Cancer Center at University of Texas

Trial Summary:

The purpose of this research study is to determine the highest dose of the drug (BMS-690514) that can be safely given to patients with advanced cancer.

Contact Information:
IN: Nasser Hanna, Site 004
Ph: 317-274-3515

TX: Roy Herbst, Site 001

For Additional Information,  Click Here


Gene Therapy for Pleural Malignancies

Phase I

Location:

Philadelphia, PA: Abramson Cancer Center of the University of Pennsylvania

Trial Summary:

This Phase I study will evaluate the safety of two doses of BG00001. Eligible subjects will have malignant pleural mesothelioma or pleural effusions who have progressed through at least one prior therapy or have refused therapy.

Contact Information:
Daniel H. Sterman, M.D. Principal Investigator

Adri Recio, RN:
Ph: 215-573-6760
Email: arecio@mail.med.upenn.edu

For Additional Information,  Click Here


FR901228 and Flavopiridol in Treating Patients with Advanced Lung, Esophageal, or Pleural Cancer

Phase I

Location:

Bethesda, MD: NCI - Center for Cancer Research & Warren Grant Magnuson Clinical Center - NCI Clinical Trials Referral Office

Trial Summary:

Drugs used in chemotherapy, such as FR901228 and flavopiridol, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving FR901228 together with flavopiridol may kill more tumor cells.

Contact Information:
David Schrump, MD, Protocol chair:
Ph: 301-451-1233
Email: david_schrump@nih.gov

Clinical Trials Office - NCI - Center for Cancer Research:
Ph: 888-624-1937

Dao Nguyen:
Ph: 301-451-1233

Tricia Kunst, RN:
Ph: 301-451-1233
Email: tricia_kunst@nih.gov

Clinical Trials Office - Warren Grant Magnusen Clinical Center - NCI Clinical Trials Referral Office:
Ph: 888-NCI-1937

For Additional Information,  Click Here


Decitabine and FR901228 in Treating Patients with Advanced Lung Cancer, Esophageal Cancer, Pleural Mesothelioma, or Lung Metastases

Phase I

Location:

Bethesda, MD: NCI - Center for Cancer Research & Warren Grant Magnuson Clinical Center - NCI Clinical Trials Referral Office

Trial Summary:

This phase I trial is studying the side effects and best dose of decitabine and FR901228 in treating patients with unresectable advanced lung cancer, esophageal cancer, pleural mesothelioma, or lung metastases.

Contact Information:
David Schrump, MD, Protocol chair:
Ph: 301-451-1233
Email: david_schrump@nih.gov

NCI - Tricia Kunst, RN:
Ph: 301-451-1233
Email: tricia_kunst@nih.gov

Clinical Trials Office - Warren Grant Magnusen Clinical Center - NCI Clinical Trials Referral Office:
Ph: 888-NCI-1937

For Additional Information,  Click Here


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