Clinical Trials Logo

Hodgkin Disease clinical trials

View clinical trials related to Hodgkin Disease.

Filter by:

NCT ID: NCT00754286 Completed - Lymphoma Clinical Trials

A Randomized Trial of The Effectiveness of Aromatherapy on Chemotherapy Induced Nausea and Vomiting in Children With Cancer

Start date: July 2008
Phase: N/A
Study type: Interventional

Aromatherapy has anecdotally been reported to decrease nausea and vomiting, decrease anxiety and increase quality of life in cancer patients. Therefore, the proposed study aims to assess the effectiveness of aromatherapy versus placebo on nausea, vomiting, anxiety and quality of life among pediatric oncology patients receiving emetogenic chemotherapy.

NCT ID: NCT00742027 Completed - Clinical trials for Classical Hodgkin's Lymphoma

Phase II Study of Oral Panobinostat in Adult Participants With Relapsed/Refractory Classical Hodgkin's Lymphoma

Start date: September 16, 2008
Phase: Phase 2
Study type: Interventional

This study evaluated the efficacy of oral panobinostat in participants with refractory/relapsed classical Hodgkins lymphoma (HL) who have received prior treatment with high dose chemotherapy and autologous stem cell transplant. Safety of panobinostat also was assessed. Other markers that may correlate with efficacy or safety were explored.

NCT ID: NCT00741871 Completed - Hodgkin's Lymphoma Clinical Trials

A Phase 1 Study of SB1518 for the Treatment of Advanced Lymphoid Malignancies

Start date: July 2008
Phase: Phase 1
Study type: Interventional

This is a Phase 1 dose escalation study to determine the maximum tolerated dose and the dose limiting toxicities of SB1518 when given alone once daily by mouth to subjects with advanced lymphoid malignancies.

NCT ID: NCT00733824 Completed - Clinical trials for Lymphoma, Non-Hodgkin

Intravenous AMD3100 for Collection of Autologous Peripheral Blood Stem Cells in Patients With Lymphoma

Start date: November 2008
Phase: Phase 1/Phase 2
Study type: Interventional

This study will evaluate the safety and efficacy of intravenous AMD3100 added to a standard G-CSF mobilization regimen of patients undergoing autologous stem cell transplantation for lymphoma. We hypothesize that after stem cell mobilization with G-CSF plus IV AMD3100, a significantly higher proportion of lymphoma patients will collect ≥ 2 x 10E6 CD34+ cells/kg.

NCT ID: NCT00724984 Completed - Lymphoma Clinical Trials

Study of the Safety and Tolerability of PCI-24781 in Patients With Lymphoma

PCYC-0403
Start date: July 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The first part of the study will determine the highest dose of study drug that can be taken without causing serious side effects in patients with lymphoma. The appropriate dose determined from the first part of the study will be used in the second part of the study to assess disease response in 2 different types of lymphoma patients.

NCT ID: NCT00722488 Completed - Multiple Myeloma Clinical Trials

Study of MLN4924, a Novel Inhibitor of Nedd8 Activating Enzyme, in Adult Patients With Lymphoma or Multiple Myeloma

Start date: June 2008
Phase: Phase 1
Study type: Interventional

This is an open-label, multicenter, phase 1, dose escalation study of MLN4924 in adult patients with lymphoma or multiple myeloma. The patient population will consist of adults with a confirmed diagnosis of lymphoma (Waldenstrom's macroglobulinemia is permitted) or multiple myeloma that is relapsed and/or refractory after at least 2 prior standard chemotherapeutic regimens and for which no curative option exists. Patients in the expansion cohort, Schedule E, must specifically have Hodgkin lymphoma, DLBCL-GCB subtype, DLBCL-non-GCB subtype, or Mantle Cell Lymphoma (MCL). Patients with multiple myeloma will no longer be evaluated as a part of this study.

NCT ID: NCT00718757 Completed - Clinical trials for Acute Lymphoblastic Leukemia

Irinotecan, Vincristine, and Dexamethasone In Children With Relapsed And/Or Refractory Hematologic Malignancies

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

The purpose of this study is to estimate the maximum tolerated dose of dexamethasone given for 5 consecutive days when combined with fixed doses of irinotecan (given IV, qd x 5, 2 days off, qd x 5) and vincristine (given IV, 2 doses total on days 1 and 8 of schedule) in children with relapsed or refractory hematologic malignancies. In addition we will also study the pharmacokinetics of irinotecan when given without and then with dexamethasone in each patient, evaluate the relationship between irinotecan pharmacokinetic parameters and toxicity and describe any antitumor effects.

NCT ID: NCT00713882 Completed - Hodgkins Disease Clinical Trials

Health and Psychosocial Outcomes in Long-Term Lymphoma Survivors

Start date: April 2008
Phase: N/A
Study type: Observational

The aims and objectives of this research are to identify chronic health conditions, psychological disease, quality of life issues, and patient preferences for survivorship care in patients who have survived aggressive lymphoma. Subjects will be asked to participate in an oral interview with the primary investigator, either in-person or over the telephone. It is estimated that the survey will take about an hour.

NCT ID: NCT00709592 Completed - Multiple Myeloma Clinical Trials

Reduced Intensity Total Body Irradiation + Thymoglobulin Followed by Allogeneic PBSCT

Start date: July 21, 2008
Phase: Phase 2
Study type: Interventional

One of two different doses of thymoglobulin will allow bone marrow engraftment with minimal Graft-versus-Host Disease and allow adequate immune response to allow the transplanted stem cells to replace the tumor cells.

NCT ID: NCT00705250 Completed - Lymphoma Clinical Trials

Bendamustine HCL in Relapsed and Primary Refractory Hodgkin Lymphoma

Start date: June 2008
Phase: Phase 2
Study type: Interventional

The standard treatment for patients with HL that has not responded to treatment or has come back after treatment is stem cell transplant. When patients are not eligible for transplant or when HL comes back after transplant, there are no standard treatment options. These patients can receive chemotherapy or participate in clinical trials. Bendamustine HCl is a chemotherapy agent that is effective in treating patients with various diseases, including non-Hodgkin's lymphoma, multiple myeloma, and breast cancer. It was recently approved for the treatment of chronic lymphocytic leukemia. In addition, small studies from Eastern Europe have shown that bendamustine HCl is likely effective for treating HL. This study will find out the effect of bendamustine HCl for transplant-ineligible patients with HL that has not responded to or has come back after treatment.