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Non-Hodgkin's Lymphoma clinical trials

View clinical trials related to Non-Hodgkin's Lymphoma.

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NCT ID: NCT00220285 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Study for Evaluation of Efficacy and Safety of SH L 749 to Indolent B-cell Non-Hodgkin's Lymphoma

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

The purpose of this study is to investigate the antitumor effect and safety of the product for relapsed or refractory indolent B-cell non-Hodgkin's lymphomas.

NCT ID: NCT00201877 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Velcade (Bortezomib, PS-341) and Rituximab in Relapsed/Refractory Mantle Cell and Follicular Non-Hodgkin's Lymphoma

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

This study will determine the overall response rate and toxicity of rituximab and Velcade in combination in patients with relapsed or refractory mantle cell non-Hodgkin's lymphoma.

NCT ID: NCT00201669 Completed - Clinical trials for Non-Hodgkin's Lymphoma

A Phase II Study of Clofarabine in Patients With Aggressive Non-Hodgkin's Lymphoma

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

This study will determine the efficacy of clofarabine as measured by response rate in patients with aggressive non-Hodgkin's lymphoma

NCT ID: NCT00201318 Completed - Clinical trials for Non-Hodgkin's Lymphoma

A Randomized Study in Non-Hodgkin's Lymphoma Patients Carrying Hepatitis B Surface Antigen

Start date: September 2001
Phase: Phase 2
Study type: Interventional

* AIMS OF THE STUDY (STUDY OBJECTIVES) 1. To test the effect of daily lamivudine (100 mg) in reducing the risk of HBV reactivation and hepatitis development in HBsAg (+) NHL patients. 2. To test the efficacy of daily lamivudine in preventing and treating hepatitis B reactivation and in circumventing hepatic failure and death. 3. To test whether lamivudine can improve the overall outcome of NHL patients who are HBV carriers. (Study end-points: The major end-point: hepatitis B reactivation in NHL patients---defined by higher than 10-fold increase of serum HBV DNA level and/or reappearance of HBeAg in the serum during and within 6 months after chemotherapy. The minor end-point I : events of hepatic failure and death---defined by jaundice with hepatic encephalopathy. The minor end-point II: the response rate and survival rate in HBsAg-positive NHL patients receiving lamivudine prophylaxis and treatment.)

NCT ID: NCT00192764 Completed - Clinical trials for Non-Hodgkin's Lymphoma

High Dose CHOP in Lymphoma

Start date: December 1996
Phase: Phase 2
Study type: Interventional

The study hypothesis is that intensification of CHOP by dose escalation of the most active drugs in the combination will improve treatment outcome. Patients with diffuse large-cell lymphoma are treated by high cyclophosphamide containing CHOP. The planned dose is 3000 mg/m2 which is 4 times the atandard one. Only 4 cycles are given.

NCT ID: NCT00184080 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Elsamitrucin (SPP 28090) in Patients With Relapsed or Refractory Non-Hodgkin's Lymphoma

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

The purpose of this study is to evaluate the safety of an experimental drug called Elsamitrucin in people with non-Hodgkin's lymphoma and to see if it can shrink their tumors. Elsamitrucin has not been approved by the Food and Drug Administration (FDA). However, the FDA is permitting the use of this drug for this study.

NCT ID: NCT00184002 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Doxorubicin (Doxil) Combined With Rituxan, Cyclophosphamide, Vincristine and Prednisone in Newly Diagnosed Aggressive Non-Hodgkin's Lymphomas

Start date: January 10, 2003
Phase: Phase 2
Study type: Interventional

The current standard treatment for non-Hodgkin's lymphoma involves drugs called cyclophosphamide, doxorubicin, vincristine, prednisone and rituxan in a regimen called "R-CHOP." Using R-CHOP therapy, complete disappearance of disease is expected in over 50% of people. One of the active drugs in the R-CHOP regimen, doxorubicin, has previously been reformulated and been placed in a fatty bubble called a liposome. The reason for placing the drug in the liposome is that there is evidence that the liposome is better taken up by tumors. This liposomally encapsulated form of doxorubicin called Doxil has shown similar or better anti-tumor against certain tumors with reduced side effects. Doxil is FDA approved for ovarian cancer. However its use in non-Hodgkin's lymphoma is still investigational. By substituting Doxil for doxorubicin in the R-CHOP regimen, it is hoped this treatment will be better at shrinking tumors and with reduced side effects. The purpose of this study is to see how well the combination of Doxil, rituximab, cyclophosphamide, vincristine and prednisone (DR-COP) are in shrinking tumors in patients with non-Hodgkin's lymphoma.

NCT ID: NCT00163761 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Efficacy Study of Outpatient Therapy for Lymphoma

Start date: December 2002
Phase: Phase 2
Study type: Interventional

This is a Phase II trial evaluating the efficacy (overall response rate) of a risk-adjusted outpatient based approach to lymphoma salvage therapy with vinorelbine, gemcitabine and pegfilgrastim and/or gemcitabine, ifosfamide, vinorelbine and pegfilgrastim.

NCT ID: NCT00163748 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Efficacy and Treatment Related Toxicity Study of a New Regimen for Lymphoma

Start date: February 2001
Phase: Phase 2
Study type: Interventional

This is an open label pilot study of 40 evaluable patients receiving vinorelbine-gemcitabine combination chemotherapy with filgrastim support in an outpatient setting. Participating patients at the time of registration will have measurable relapsed or primary refractory lymphoma.

NCT ID: NCT00162955 Completed - Clinical trials for Non-Hodgkin's Lymphoma

Prevention of CHOP-induced Chronic Cardiotoxicity

Start date: May 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the protective effect of Valsartan on chronic cardiotoxicity induced by CHOP.