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Neoplasms, Plasma Cell clinical trials

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NCT ID: NCT00574288 Completed - Multiple Myeloma Clinical Trials

Daratumumab (HuMax®-CD38) Safety Study in Multiple Myeloma

Start date: March 26, 2008
Phase: Phase 2
Study type: Interventional

Establishment of safety profile of HuMax-CD38 when given as monotherapy in participants with multiple myeloma relapsed from or refractory to at least 2 different cytoreductive therapies and without further established treatment options.

NCT ID: NCT00572338 Completed - Multiple Myeloma Clinical Trials

Therapeutic Research in Multiple Myeloma

Start date: August 2003
Phase: N/A
Study type: Observational

The purpose of this study is to learn how myeloma cells grow and become a cancer, how to distinguish them from normal cells and how to eliminate these cells selectively.

NCT ID: NCT00570180 Completed - Multiple Myeloma Clinical Trials

Combination Bortezomib-containing Regimens in Newly Diagnosed Patients With t (4; 14) Positive Multiple Myeloma

Start date: August 25, 2008
Phase: Phase 2
Study type: Interventional

Given the disappointing results with routine ASCT in t(4;14) patients, we propose this open label phase II study of bortezomib along with dexamethasone and pegylated liposomal doxorubicin (Doxil/Caelyx), referred to as the DBd regimen, for 4 cycles, followed by post-induction therapy with cyclophosphamide + bortezomib + prednisone (referred to as the CyBorP regimen) for 8 cycles. Since patients with t(4;14) remain at high risk for relapse, maintenance therapy with dexamethasone weekly will be given until disease progression.

NCT ID: NCT00569868 Completed - MULTIPLE MYELOMA Clinical Trials

UARK 2005-05, Coagulation-Related Effects of Velcade Treatment in Patients With Relapsed or Refractory Multiple Myeloma

Start date: August 2005
Phase: N/A
Study type: Interventional

To evaluate changes in coagulation (blood clotting) factors and platelet function in multiple myeloma participants undergoing VELCADE treatment for the first time.

NCT ID: NCT00569309 Completed - Lymphoma Clinical Trials

Immune Reconstitution After Autologous Hematopoietic Stem Cell Transpl for High-Risk Lymphoma

Start date: December 12, 2007
Phase: N/A
Study type: Interventional

RATIONALE: Vaccines may help the body build an effective immune response to kill cancer cells. Giving vaccine therapy after an autologous stem cell transplant may kill any cancer cells that remain after transplant. PURPOSE: This clinical trial is studying how well vaccine therapy works in treating patients who have undergone autologous stem cell transplant for high-risk lymphoma or multiple myeloma.

NCT ID: NCT00568880 Completed - Clinical trials for Multiple Myeloma and Plasma Cell Neoplasm

Hydroxychloroquine and Bortezomib in Treating Patients With Relapsed or Refractory Multiple Myeloma

Start date: September 8, 2010
Phase: Phase 1
Study type: Interventional

RATIONALE: Drugs used in chemotherapy, such as hydroxychloroquine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving hydroxychloroquine together with bortezomib may kill more cancer cells. PURPOSE: This phase I/II trial is studying the side effects and best dose of hydroxychloroquine when given together with bortezomib and to see how well it works in treating patients with relapsed or refractory multiple myeloma.

NCT ID: NCT00566098 Completed - Clinical trials for Multiple Myeloma and Plasma Cell Neoplasm

Activated White Blood Cells With ASCT for Newly Diagnosed Multiple Myeloma

Start date: November 2007
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Activating white blood cells in the laboratory may help them kill more cancer cells when they are put back in the body. This may be an effective treatment for patients undergoing a stem cell transplant for multiple myeloma. PURPOSE: This phase I/II trial is studying the side effects of activated white blood cells and to see how well they work in treating patients who are undergoing a stem cell transplant for newly diagnosed stage II or stage III multiple myeloma.

NCT ID: NCT00564889 Completed - Clinical trials for Multiple Myeloma and Plasma Cell Neoplasm

Lenalidomide, Cyclophosphamide, and Dexamethasone in Treating Patients With Primary Systemic Amyloidosis

Start date: December 2007
Phase: Phase 2
Study type: Interventional

RATIONALE: Biological therapies, such as lenalidomide, may stimulate the immune system in different ways and stop plasma cells from growing. Drugs used in chemotherapy, such as cyclophosphamide and dexamethasone, work in different ways to stop the growth of plasma cells, either by killing the cells or by stopping them from dividing. Giving lenalidomide together with cyclophosphamide and dexamethasone may be an effective treatment for primary systemic amyloidosis. PURPOSE: This phase II trial is studying how well giving lenalidomide together with cyclophosphamide and dexamethasone works in treating patients with primary systemic amyloidosis.

NCT ID: NCT00564200 Completed - Multiple Myeloma Clinical Trials

MINIALO-VELCADE2005: A Study of Bortezomib (Velcade) Treated Multiple Myeloma Patients Pre and Post Allogeneic Haematopoietic Progenitor Cell Transplant With no Myeloablative Conditioning

MINIALO-VELCAD
Start date: November 2007
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to analyze the efficacy of allogeneic bone marrow transplantation in a reduced-intensity manner combined with bortezomib in the treatment of multiple myeloma with bad prognosis, in order to evaluate the response and relapse rates

NCT ID: NCT00562224 Completed - Multiple Myeloma Clinical Trials

Study of the Safety and Tolerability of Oral Capsule Form of PCI-24781 in Advanced Cancer Patients

Start date: November 2007
Phase: Phase 1
Study type: Interventional

To determine the highest dose of study drug that can be taken without causing serious side effects in patients with advanced cancer. The study will look at safety of the study drug and whether the treatment schedule is tolerated by patients.