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Neoplasms, Plasma Cell clinical trials

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NCT ID: NCT00290095 Completed - Multiple Myeloma Clinical Trials

Quality of Life in Patients With Multiple Myeloma

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

The purpose of this study is to determine Clinically important difference and Response shift in quality of life in patients with Multiple Myeloma.

NCT ID: NCT00288028 Completed - Clinical trials for Multiple Myeloma and Plasma Cell Neoplasm

Bortezomib in Treating Patients With Multiple Myeloma Who Have Undergone an Autologous Peripheral Blood Stem Cell Transplant

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

RATIONALE: Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving bortezomib after an autologous peripheral blood stem cell transplant may stop the growth of any cancer cells that remain after transplant. PURPOSE: This phase I trial is studying the side effects and best dose of bortezomib in treating patients with multiple myeloma who have undergone an autologous peripheral blood stem cell transplant.

NCT ID: NCT00287872 Completed - Multiple Myeloma Clinical Trials

Bortezomib and Thalidomide in Treating Patients With Newly Diagnosed Stage II or Stage III Multiple Myeloma

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

RATIONALE: 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 blocking blood flow to the cancer. Giving bortezomib together with thalidomide may kill more cancer cells. PURPOSE: This phase II trial is studying how well giving bortezomib together with thalidomide works in treating patients with newly diagnosed stage II or stage III multiple myeloma.

NCT ID: NCT00281879 Terminated - Lymphoma Clinical Trials

Donor Stem Cell Transplant or Donor White Blood Cell Infusions in Treating Patients With Hematologic Cancer

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

RATIONALE: A peripheral stem cell transplant or an umbilical cord blood transplant from a donor may be able to replace blood-forming cells that were destroyed by chemotherapy or radiation therapy. Giving an infusion of the donor's white blood cells (donor lymphocyte infusion) after the transplant may help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells can make an immune response against the body's normal cells. Methotrexate, cyclosporine, tacrolimus, or methylprednisolone may stop this from happening. PURPOSE: This clinical trial is studying how well a donor stem cell transplant or donor white blood cell infusions work in treating patients with hematologic cancer.

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: NCT00275262 Terminated - Multiple Myeloma Clinical Trials

A Study to Evaluate the Ability of Lupron Depot to Enhance Immune Function Following Bone Marrow Transplantation

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

Phase 2 study, conducted in patients with Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma, or mantle cell lymphoma undergoing high-dose chemotherapy and autologous stem cell transplantation.

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.