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Multiple Myeloma clinical trials

View clinical trials related to Multiple Myeloma.

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NCT ID: NCT01206205 Completed - Multiple Myeloma Clinical Trials

Frontline Therapy in de Novo Multiple Myeloma Patients Under 65

IFM2008
Start date: August 2009
Phase: Phase 2
Study type: Interventional

The purpose of this Phase 2 study is to evaluate the efficacy and safety of treatment with bortezomib, lenalidomide and dexamethasone in patients with untreated multiple myeloma. This study will evaluate whether the addition of lenalidomide to bortezomib and dexamethasone will increase the Complete Response (CR)/ very good partial response (VGPR) rate before and after High Dose Therapy (HDT) with ASCT.

NCT ID: NCT01204164 Completed - Multiple Myeloma Clinical Trials

Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies

TG02-101
Start date: August 2010
Phase: Phase 1
Study type: Interventional

This is a multicenter, open-label, dose escalation Phase 1 study.

NCT ID: NCT01199562 Completed - Clinical trials for Chronic Myelomonocytic Leukemia

Infection Prophylaxis and Management in Treating Cytomegalovirus (CMV) Infection in Patients With Hematologic Malignancies Previously Treated With Donor Stem Cell Transplant

Start date: December 2010
Phase:
Study type: Observational

RATIONALE: Infection prophylaxis and management may help prevent cytomegalovirus (CMV) infection caused by a stem cell transplant. PURPOSE:This clinical trial studies infection prophylaxis and management in treating cytomegalovirus infection in patients with hematologic malignancies previously treated with donor stem cell transplant.

NCT ID: NCT01198457 Completed - Multiple Myeloma Clinical Trials

Study to Investigate Adherence of Patients to Clodronate (Bonefos) Treatment

BONA
Start date: January 2009
Phase: N/A
Study type: Observational

Adherence (or compliance with) a medication regimen is generally defined as the extent to which patients take medication as prescribed by their health care providers. The adherence to medications has close relation to effectiveness of the therapy. The primary objective of this study is to observe the adherence to treatment with oral clodronate (PDC, proportion of days covered, number of days in which clodronate is taken according to treating physician recommendation) in patients with malignancy. The secondary "hypothesis generating" objective is to describe the relation between adherence to treatment with oral clodronate and efficacy of the therapy (skeletal events, pain).

NCT ID: NCT01191060 Completed - Myeloma Clinical Trials

Study Comparing Conventional Dose Combination RVD to High-Dose Treatment With ASCT in the Initial Myeloma up to 65 Years

IFM/DFCI2009
Start date: October 2010
Phase: Phase 3
Study type: Interventional

Objective of this study is to determine if, in the era of novel drugs, high dose therapy (HDT) is still necessary in the initial management of multiple myeloma in younger patients. HDT as compared to conventional dose treatment would be considered superior if it significantly prolongs Progression-free survival (by at least 9 months).

NCT ID: NCT01190787 Completed - Multiple Myeloma Clinical Trials

Subcutaneous Velcade Plus Oral Melphalan and Prednisone or Plus Cycloposphamide and Prednisone or Plus Prednisone

Start date: July 2010
Phase: Phase 2
Study type: Interventional

This protocol is a single-arm, three-cohort, phase II multicenter study designed to assess the safety and the efficacy of three all-oral combinations: Velcade with continuous low-dose melphalan and prednisone (VMP) or with continuous low-dose cyclophosphamide and prednisone (VCP) or Velcade with low-dose prednisone could be effective and well tolerated (VP).

NCT ID: NCT01183949 Completed - Multiple Myeloma Clinical Trials

Effect of AT7519M Alone and AT7519M Plus Bortezomib in Patients With Previously Treated Multiple Myeloma

Start date: November 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether AT7519M alone or AT7519M plus bortezomib are effective treatments in patients with previously treated multiple myeloma.

NCT ID: NCT01177735 Completed - Multiple Myeloma Clinical Trials

Pomalidomide in Gene Expression Profiling (GEP)-Defined High-risk Multiple Myeloma

Start date: October 2011
Phase: Phase 2
Study type: Interventional

This is a phase II study, open-label, single institution trial of pomalidomide in GEP-defined, high-risk relapsing/refractory multiple myeloma. Prior therapy must have included lenalidomide. Patient accrual is 30 over a 2 year period. Primary objective: - To determine progression-free survival (PFS) after initiation of pomalidomide therapy Secondary objective: - To determine the response rate (CR, n-CR, VGPR) and duration of response after pomalidomide therapy. - To determine gene expression profiling (GEP) changes exerted within 48 hours of initiation of daily pomalidomide dosing. - To determine gene expression profiling (GEP) changes exerted within 48 hours of initiation 3 concurrent days of exposure to lenalidomide. - To determine MRI- and PET-CT-defined CR in studies obtained at baseline and every 6 month examinations.

NCT ID: NCT01177397 Completed - Multiple Myeloma Clinical Trials

Study to Assess Safety, Pharmacokinetics, and Efficacy of Oral CC-223 for Patients With Advanced Solid Tumors, Non-Hodgkin Lymphoma or Multiple Myeloma

Start date: July 20, 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The main purpose of this first human study with CC-223 is to assess the safety and action of a new class of experimental drug (dual mTOR inhibitors) in patients with advanced tumors unresponsive to standard therapies and to determine the appropriate dose and tumor type for later-stage clinical trials.

NCT ID: NCT01177371 Completed - Clinical trials for Recurrent Mantle Cell Lymphoma

High-Dose Busulfan and High-Dose Cyclophosphamide Followed By Donor Bone Marrow Transplant in Treating Patients With Leukemia, Myelodysplastic Syndrome, Multiple Myeloma, or Recurrent Hodgkin or Non-Hodgkin Lymphoma

Start date: March 1988
Phase: Phase 2
Study type: Interventional

RATIONALE: Giving high doses of chemotherapy drugs, such as busulfan and cyclophosphamide, before a donor bone marrow transplant helps stop the growth of cancer cells. It may also 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. Sometimes the transplanted cells from a donor can make an immune response against the body's normal cells. Giving cyclosporine, methylprednisolone, and methotrexate after transplant may stop this from happening. PURPOSE: This clinical trial studies high-dose busulfan and high-dose cyclophosphamide followed by donor bone marrow transplant in treating patients with leukemia, myelodysplastic syndrome, multiple myeloma, or recurrent Hodgkin or Non-Hodgkin lymphoma.