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Neoplasms, Plasma Cell clinical trials

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NCT ID: NCT00281814 Completed - Lymphoma Clinical Trials

Caregiver Support in the Coping of Patients Who Are Undergoing a Donor Bone Marrow Transplant

Start date: February 1, 2006
Phase: N/A
Study type: Observational

RATIONALE: Questionnaires that measure coping may improve the ability to plan supportive care for patients undergoing donor bone marrow transplant. PURPOSE: This clinical trial is studying coping in patients who are undergoing a donor bone marrow transplant.

NCT ID: NCT00281801 Completed - Lymphoma Clinical Trials

Caregiver Support in the Quality of Life of Patients Who Are Undergoing Donor Bone Marrow Transplantation

Start date: February 2006
Phase: N/A
Study type: Observational

RATIONALE: Questionnaires that measure quality-of-life may improve the health care team's ability to plan supportive care for patients undergoing donor bone marrow transplantation. PURPOSE: This clinical trial is studying quality of life in patients who are undergoing donor bone marrow transplantation.

NCT ID: NCT00281476 Completed - Multiple Myeloma Clinical Trials

The Effect of High Dose Simvastatine on Multiple Myeloma

Start date: February 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is to evaluate the effect of high doses of Simvastatine on bone metabolisme and biochemical markers of disease in Multiple Myeloma

NCT ID: NCT00270101 Completed - Multiple Myeloma Clinical Trials

The Effect of Epoetin Alfa on the Anemia of Patients With Multiple Myeloma

Start date: January 1995
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of epoetin alfa versus placebo in reducing the transfusion requirements in anemic patients with multiple myeloma, and to investigate the quality-of-life benefits associated with the use of epoetin alfa. Epoetin alfa is a genetically engineered protein that stimulates red blood cell production.

NCT ID: NCT00265837 Completed - Lymphoma Clinical Trials

Laboratory-Treated Donor Bone Marrow in Treating Patients Who Are Undergoing a Donor Bone Marrow Transplant for Hematologic Cancer

Start date: December 2002
Phase: Phase 3
Study type: Interventional

RATIONALE: Giving chemotherapy and total-body irradiation before a donor bone marrow transplant or peripheral blood stem cell transplant helps stop the growth of cancer and abnormal cells and helps stop the patient's immune system from rejecting the donor's stem cells. When certain stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. Sometimes the transplanted cells from a donor can make an immune response against the body's normal cells. Removing the T cells from the donor cells before transplant may stop this from happening. PURPOSE: This randomized phase III trial is studying donor bone marrow that is treated in the laboratory using two different devices to compare how well they work in treating patients who are undergoing a donor bone marrow transplant for hematologic cancer.

NCT ID: NCT00263484 Completed - Multiple Myeloma Clinical Trials

Higher Frequency Zoledronic Acid in the Treatment of Multiple Myeloma

dtZ
Start date: December 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether lower than conventional doses of dexamethasone and thalidomide; and a higher dosing frequency of zoledronic acid are effective in the treatment of newly-diagnosed multiple myeloma.

NCT ID: NCT00259740 Completed - Clinical trials for Relapsed or Plateau-Phase Multiple Myeloma

Open-Label, Phase 2, Proof of Concept Study in Multiple Myeloma - Denosumab

Start date: November 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if denosumab is effective in the treatment of relapsed or plateau-phase multiple myeloma.

NCT ID: NCT00258245 Completed - Clinical trials for Multiple Myeloma and Plasma Cell Neoplasm

Arsenic Trioxide and Ascorbic Acid Combined With Bortezomib, Thalidomide, and Dexamethasone in Treating Patients With Relapsed or Refractory Multiple Myeloma or Plasma Cell Leukemia

Start date: May 2005
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as arsenic trioxide and dexamethasone, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Ascorbic acid may help arsenic trioxide work better by making cancer cells more sensitive to the drug. Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Thalidomide may stop the growth of cancer cells by stopping blood flow to the cancer. Giving arsenic trioxide and ascorbic acid together with bortezomib, thalidomide, and dexamethasone may stop the growth of and kill more cancer cells. PURPOSE: This phase I trial is studying the side effects and best dose of arsenic trioxide when given together with ascorbic acid, bortezomib, thalidomide, and dexamethasone in treating patients with relapsed or refractory multiple myeloma or plasma cell leukemia.

NCT ID: NCT00258206 Completed - Clinical trials for Multiple Myeloma and Plasma Cell Neoplasm

Rituximab and Cyclophosphamide in Treating Patients With High Risk, Refractory, or Relapsed Multiple Myeloma

Start date: December 2004
Phase: Phase 2
Study type: Interventional

RATIONALE: Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Drugs used in chemotherapy, such as cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving rituximab together with cyclophosphamide may kill more cancer cells. PURPOSE: This phase II trial is studying how well giving rituximab together with cyclophosphamide works in treating patients with high risk, refractory, or relapsed multiple myeloma.

NCT ID: NCT00257114 Completed - Multiple Myeloma Clinical Trials

Evaluation of VELCADE Given as Retreatment to Multiple Myeloma Patients for Efficacy, Safety and Tolerability

Start date: n/a
Phase: Phase 4
Study type: Interventional

Multiple myeloma represents the second most common hematological malignancy.VELCADE is a small molecule to treat human malignancies. Its anti-neoplastic effect invovles several distinct mechanisms including inhibition of cell growth. Patients who have relapsed or are refractory to therapy, the standard of care is now VELCADE based on the results of previous clinical trials.