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Neoplasms, Plasma Cell clinical trials

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NCT ID: NCT00256776 Terminated - Multiple Myeloma Clinical Trials

MMVAR - Velcade: Study of Velcade for the Treatment of Myeloma Patients After Autologous Transplantation

Start date: July 2005
Phase: Phase 3
Study type: Interventional

This is an international study in adult patients diagnosed with multiple myeloma who have already received at least one autologous stem cell transplantation and who have responded but later progressed, or relapsed, at least one year after transplantation. Eligible patients will be randomly assigned to one of two treatments: either Velcade plus Thalidomide plus Dexamethasone or Thalidomide plus Dexamethasone. Thalidomide and Velcade are two new agents that have recently become available for the treatment of multiple myeloma, especially in relapsed patients. This study therefore aims to test the hypothesis that the combination treatment with Velcade plus Thalidomide plus Dexamethasone will result in a longer time to progression (measure of time after the disease is treated until it starts to get worse) than Thalidomide plus Dexamethasone alone.

NCT ID: NCT00253552 Terminated - Lymphoma Clinical Trials

G-CSF-Treated Donor Bone Marrow Transplant in Treating Patients With Hematologic Disorders

Start date: May 2004
Phase: N/A
Study type: Interventional

RATIONALE: Giving chemotherapy drugs and total-body irradiation before a donor bone marrow 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 the healthy 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. Giving colony-stimulating factors, such as G-CSF, to the donor helps the stem cells move from the bone marrow to the blood so they can be collected and stored. PURPOSE: This clinical trial is studying how well a G-CSF-treated donor bone marrow transplant works in treating patients with hematologic cancer or noncancer.

NCT ID: NCT00243763 Terminated - Multiple Myeloma Clinical Trials

TKI258 in Subjects With Refractory or Relapsed Multiple Myeloma

Start date: n/a
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to determine the maximum tolerated dose (MTD), dose limiting toxicity (DLT), and safety profile of CHIR-258 when administered to subjects with refractory or relapsed multiple myeloma (MM).

NCT ID: NCT00243035 Terminated - Clinical trials for Refractory Multiple Myeloma

Tipifarnib and Bortezomib in Treating Patients With Relapsed Multiple Myeloma

Start date: August 2005
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II trial is studying the side effects and best dose of tipifarnib when given together with bortezomib and to see how well they work in treating patients with relapsed multiple myeloma. Tipifarnib and bortezomib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving tipifarnib together with bortezomib may kill more cancer cells.

NCT ID: NCT00242827 Terminated - Myeloma Clinical Trials

Efficacy and Safety of Oral CEP-701 for the Treatment of Patients With Advanced Multiple Myeloma

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

An Open-Label Study of the Efficacy and Safety of Oral CEP-701 for the Treatment of Patients with Advanced Multiple Myeloma.

NCT ID: NCT00241371 Terminated - Multiple Myeloma Clinical Trials

A Phase II Study of Clofarabine in Patients With Relapsed or Refractory Multiple Myeloma

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

To determine the overall response rate (CR+PR) of patients with relapsed or refractory multiple myeloma treated with clofarabine.

NCT ID: NCT00240162 Terminated - Multiple Myeloma Clinical Trials

PTK/ZK as Post Transplant Maintenance Therapy in Patients With Multiple Myeloma

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

The purpose of this study it to evaluate the efficacy of PTK787/ZK 222584, in inducing at least a 50% reduction in paraprotein in patients with multiple myeloma whose paraprotein levels are < 5 g/dL following high dose chemotherapy (HDCT) and autologous stem cell transplantation (ASCT).

NCT ID: NCT00227682 Terminated - Clinical trials for Multiple Myeloma and Plasma Cell Neoplasm

Arsenic Trioxide, Thalidomide, Dexamethasone, and Ascorbic Acid in Treating Patients With Relapsed or Refractory Multiple Myeloma

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

RATIONALE: Drugs used in chemotherapy, such as arsenic trioxide, dexamethasone, and ascorbic acid, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more cancer cells. Sometimes when chemotherapy is given, it does not stop the growth of cancer cells. The cancer is said to be resistant to chemotherapy. Giving arsenic trioxide together with chemotherapy may reduce drug resistance and allow the cancer cells to be killed. Thalidomide may stop the growth of multiple myeloma by blocking blood flow to the cancer. Giving arsenic trioxide together with thalidomide, dexamethasone, and ascorbic acid may kill more cancer cells. PURPOSE: This phase II trial is studying how well giving arsenic trioxide together with thalidomide, dexamethasone, and ascorbic acid works in treating patients with relapsed or refractory multiple myeloma.

NCT ID: NCT00216151 Terminated - Multiple Myeloma Clinical Trials

Zoledronic Acid in the Management of Patients With Asymptomatic/Early Stage Multiple Myeloma

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

Evidence for the beneficial effects of bisphosphonates on bone resorption in multiple myeloma has been reported extensively, showing reductions in skeletal events and improvement of several biochemical variables in bone resorption. Zoledronic acid (Zometa®, CGP42446) is the most potent clinically available bisphosphonates, with the largest therapeutic ratio between the desired inhibition of calcium resorption and the unwanted inhibition of mineralization in vitro of all the bisphosphonates. This trial will investigate the efficacy of zoledronic acid in preventing skeletal events in patients with asymptomatic/early stage Multiple Myeloma

NCT ID: NCT00200668 Terminated - Multiple Myeloma Clinical Trials

Comparison Between FDG-PET and MRI for the Assessment of Response to Intensive Chemotherapy in Multiple Myeloma Patients.

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

Comparison between FDG-PET and MRI for the assessment of response to intensive chemotherapy in multiple myeloma patients.