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Lymphoma clinical trials

View clinical trials related to Lymphoma.

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NCT ID: NCT01789723 Withdrawn - Clinical trials for Non Hodgkin's Lymphoma

Phase 1 Study of Fusilev to Prevent or Reduce Mucositis in Patients With Non-Hodgkin's Lymphoma Receiving Folotyn

Start date: March 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is determine the optimal dose and schedule of Fusilev to prevent or reduce Mucositis in patients with Non-Hodgkin's Lymphoma receiving Folotyn treatment.

NCT ID: NCT01789255 Completed - Clinical trials for Chronic Myelomonocytic Leukemia

Vorinostat, Tacrolimus, and Methotrexate in Preventing GVHD After Stem Cell Transplant in Patients With Hematological Malignancies

Start date: June 2013
Phase: Phase 2
Study type: Interventional

This pilot phase II trial studies how well giving vorinostat, tacrolimus, and methotrexate works in preventing graft-versus-host disease (GVHD) after stem cell transplant in patients with hematological malignancies. Vorinostat, tacrolimus, and methotrexate may be an effective treatment for GVHD caused by a bone marrow transplant.

NCT ID: NCT01789060 Completed - Malignant Lymphoma Clinical Trials

p-AKT Expression on Clinical Outcomes in Malignant Lymphoma

Start date: December 2012
Phase: N/A
Study type: Observational

PI3K(phosphatidylinositol 3-kinase)/AKT pathway is an important oncogenic signaling pathway. However, clinical information about the significance of p-AKT expression in malignant lymphoma is not fully understood yet. In this study, we investigated the overexpression of p-AKT and its prognostic implication in malignant lymphoma.

NCT ID: NCT01788839 Recruiting - Breast Cancer Clinical Trials

Longitudinal Sexual and Reproductive Health Study of Women With Breast Cancer and Lymphoma

Start date: February 2013
Phase:
Study type: Observational

The purpose of this study is to see how cancer treatment affects sexual and reproductive function. The patient will also be asked to participate in blood draws to see if and how cancer treatment affects the ovaries and the ability to have children (fertility). These blood draws are optional and the patient can still participate in the questionnaire portion of the study even if they choose not to have their blood drawn.

NCT ID: NCT01788189 Completed - B-cell Lymphoma Clinical Trials

Lenalidomide, MTX, Ara-C and Rituximab in Relapsed Aggressive B-cell Lymphomas

LeMLAR
Start date: January 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Multicenter prospective open-label non-randomised phase I/II study in patients with relapsed or refractory CD20-positive aggressive lymphomas Phase I: Dose escalation of methotrexate and cytarabine (days 1, 8 and 15 of each 28-day cycle) in a 3 + 3 design with fixed doses of lenalidomide (days 1 - 21) and rituximab (day 1), maximum 6 cycles Phase II: Treatment of 20 patients at maximum tolerated doses of phase I

NCT ID: NCT01788137 Recruiting - High Risk Clinical Trials

A Study of Improving the Efficacy of Treatment in High Risk T Cell Lymphoma Patients

Start date: January 2008
Phase: Phase 3
Study type: Interventional

This is a prospective , open, multicenter, randomized phase III study. The investigators planed to include 380 untreated high risk T cell lymphoma adults,to random to CHOP and c-ATT regimen groups after signature the informed consents. The patients will receive safety assessment every cycles, and efficacy evaluation every 3 cycles. Every-two-months follow up will be received after finishing the treatment.

NCT ID: NCT01787409 Recruiting - Clinical trials for Chronic Lymphocytic Leukemia

Cholecalciferol in Improving Survival in Patients With Newly Diagnosed Cancer With Vitamin D Insufficiency

Start date: March 6, 2013
Phase: N/A
Study type: Interventional

This partially randomized clinical trial studies cholecalciferol in improving survival in patients with newly diagnosed cancer with vitamin D insufficiency. Vitamin D replacement may improve tumor response and survival and delay time to treatment in patients with cancer who are vitamin D insufficient.

NCT ID: NCT01786135 Completed - Clinical trials for Lymphoma, Large B-Cell, Diffuse

A Safety Study of SGN-CD19A for B-Cell Lymphoma

Start date: February 2013
Phase: Phase 1
Study type: Interventional

This is a phase 1, open-label, dose-escalation, multicenter study to evaluate the safety and tolerability of SGN-CD19A in patients with relapsed or refractory B-lineage non-Hodgkin lymphoma (B-NHL)

NCT ID: NCT01786096 Completed - Burkitt Lymphoma Clinical Trials

A Safety Study of SGN-CD19A for Leukemia and Lymphoma

Start date: February 2013
Phase: Phase 1
Study type: Interventional

This is a phase 1, open-label, dose-escalation, multicenter study to evaluate the safety and tolerability of SGN-CD19A in adult and pediatric patients with relapsed or refractory B-lineage acute lymphoblastic leukemia (B-ALL), Burkitt lymphoma or leukemia, or B-lineage lymphoblastic lymphoma (B-LBL).

NCT ID: NCT01786018 Recruiting - Clinical trials for B-cell Lymphoma Refractory

Thiotepa, Busulfan and Fludarabin for pt With Refractory/Early Relapsed Aggressive B-cell Non Hodgkin Lymphomas

TBF
Start date: February 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate progression free survival, transplant-related morbidity (TRM) at day +100 and at +365, overall survival and incidence of acute and chronic GVHD in refractory/early relapsed aggressive B-cell non Hodgkin lymphomas patients treated with allogeneic Transplantation after a conditioning with Thiotepa, Busulfan and fludarabin.