Tulane Cancer Center
Clinical Research Protocols

January 2006
Tulane Office of Clinical Research
(985) 624-9683
Brain
Breast
Gastro-intestinal
Genito-urinary
Gynecological
Head & Neck
Leukemia
Liver
Lung
Lymphoma
Melanoma
Multiple Myeloma
Neuroblastoma
Soft Tissues Sarcoma
General
AIDS-related
Bone Marrow Transplant
Pediatric
Hematopoietic Failure and Genetic Disease Transplant Studies

See also: Tulane's ACCTION regional clinical trials network.
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AIDS-Related Cancers
None currently open to accrual
Brain
None currently open to accrual
Breast
None currently open to accrual
Gastro-intestinal
None currently open to accrual
Genito-urinary
None currently open to accrual
Gynecologic
None currently open to accrual
Head and Neck
None currently open to accrual
Leukemia
General
SWOG   #   9007
IRB 9/12/91
Companion to any SWOG LEUKEMIA study: Cytogenetics (marrow)
Acute
SWOG #   S0301
IRB 03/11/2004
A Phase II study of induction with Daunorubicin, Cytarabine, and Cyclosporine all by continuous IV infusion for previously untreated non-M3 acute myeloid leuemia (AML) in patients age 56 or older.
Temporary closure as of March 2004.
Tulane BMT   #   98-1
IRB 11/10/98
TRANSPLANT: Bone marrow transplant for high-risk LEUKEMIAS with busulfan, CTX, and Etoposide
* Tulane investigator-initiated study
Chronic
BMT   #   2000-01
IRB 1/25/00
CML in the first chronic phase. Allogeneic BMT for chronic myelogenous leukemia using primed bone marrow stem cells.
Tulane investigator-initiated study.

Liver
None currently open to accrual
Lung
Non-small-cell
SWOG   #   E5597
IRB 6/14/01
(Post-op, Stage IA, pT1N0 or Stage IB, pT1N0) "Phase III Chemoprevention Trial of Selenium Supplementation in Persons with Resected Stage I Non-Small-Cell Lung Cancer"

Lymphoma
Hodgkins'
SWOG   #   E2496
IRB 12/31/99
Randomized phase III trial of ABVD versus Stanford v +/- radiation therapy in locally extensive and advanced stage Hodgkin's disease with 0-2 risk factors.
Non-Hodgkins'
Tulane BMT   #   99-2
IRB 2/24/00
Autologous transplantation for non-Hodgkin's lymphoma. The role of in vivo purging with monoclonal antibody.
AIDS-related Non-Hodgkins'
SWOG   #   8947
IRB 5/10/90
Companion to SWOG S9704: Central serum repository (mandatory)
SWOG   #   9245
IRB 05/13/93
Companion to SWOG S9704: Central lymphoma repository tissue procurement protocol for relapsed or recurrent disease (optional)

Melanoma
None currently open to accrual
Multiple Myeloma
Tulane BMT   #   99-1
IRB 08/02/99
MULTIPLE MYELOMA: Immuno-transplantation for lymphoid malignancy using allogeneic blood stem cells.
Tulane   #   HSO1.02
IRB 3/12/02
MULTIPLE MYELOMA: Autologous peripheral stem cell transplantation for multiple myeloma: Safety and efficacy of the use of Rituxan for in vivo purging prior to high-dose chemotherapy and peripheral stem cell transplantation in the treatment of multiple myeloma.
* Tulane investigator-initiated.

Neuroblastoma
None currently open to accrual
Soft Tissues Sarcoma
None currently open to accrual
Hematopoietic Failure and Genetic Disease Transplant Studies
Tulane BMT   #   2001-03
IRB 7/17/2001
Phase II trial of CD34 selected peripheral blood progenitor cells with immunoablation in the treatment of severe autoimmune disease

General protocols
None currently open to accrual
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NOTICE TO ACCTION NETWORK RESEARCHERS: NIH policy requires all individuals involved in research with humans that is funded by the NIH to receive education in the protection of human research participants. To comply with this requirement, the NSABP is requiring that all NSABP investigators (any physician responsible for administering therapy and/or for consenting patients on NSABP treatment protocols) must complete training in the protection of human research participants. Acceptable forms of training include the NIH Web site training program at http://ohsr.od.nih.gov/cbt. This is also available in the Member's Area of the NSABP Web site at http://www.nsabp.pitt.edu and on the Tulane Web site at http://www.som.tulane.edu/irb/program.
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Tulane Cancer Center, Box HC-62
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New Orleans, Louisiana 70112-2699

Tulane Office of Clinical Research
(504) 988-6121, (800) 588-5800