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Lymphoma clinical trials

View clinical trials related to Lymphoma.

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NCT ID: NCT00389077 Completed - Tumors Clinical Trials

Trial of Two Schedules of Perifosine for Patients With Solid Tumors or Lymphomas

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

This is a study of the drug perifosine for patients who have no standard treatment options. This study is designed to identify which cancer types respond to perifosine, and determine which regimen of perifosine is most effective in each one. Patients with either solid tumors or with lymphomas for whom this protocol represents reasonable or optimal treatment will be randomized to receive either perifosine 100 mg daily or 900 mg weekly until disease progression. Based on currently available data it is anticipated that these doses should be easily tolerated by most patients.

NCT ID: NCT00389051 Completed - Clinical trials for Non-Hodgkin's Lymphoma

A Phase I Study of Bendamustine Hydrochloride in Patients With Indolent B-cell Non-Hodgkin's Lymphoma

Start date: October 31, 2006
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the tolerability, pharmacokinetics and antitumor effect of bendamustine hydrochloride (SyB L-0501) in patients with indolent B-cell Non-Hodgkin's Lymphoma.

NCT ID: NCT00388531 Completed - Lymphoma Clinical Trials

Depocyte in the Treatment of CNS Relapse in Patients With Lymphoblastic Leucemia or Very Aggressive Lymphoma

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

The first purpose is to confirm or not the efficacy of only one administration of DepoCyte®.

NCT ID: NCT00388349 Completed - Lymphoma Clinical Trials

Gemcitabine and Hodgkin's Disease Chemotherapy Followed by Peripheral Blood Stem Cell Rescue for Hodgkin's Disease

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

Phase II Gemcitabine + HD Chemotherapy Followed by PBSC Rescue for HD

NCT ID: NCT00388193 Completed - Clinical trials for Acute Lymphoblastic Leukemia

Rituximab Combined With Chemotherapy in Burkitt`s Lymphoma

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

The purpose of this clinical trial is to prove the efficacy of the following new regimen treatment: - Administration of anti-CD20 (Rituximab) combined with chemotherapy. - Combined treatment with high doses of methotrexate and high doses of cytarabine with conventional cytostatics (block C) - Prophylactic administration of G-CSF after all chemotherapy cycles - local irradiation after 6 cycle if CNS was affected or if there are residual tumour

NCT ID: NCT00387959 Completed - Lymphoma Clinical Trials

Chemotherapy, Radiation Therapy, Rituximab, and Umbilical Cord Blood Transplant in Treating Patients With B-Cell Non-Hodgkin's Lymphoma

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

RATIONALE: Giving low doses of chemotherapy, such as cyclophosphamide and fludarabine, total-body irradiation, and rituximab before a donor umbilical cord blood stem cell transplant helps stop the growth of cancer cells. It also stops the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune cells and help destroy any remaining cancer cells (graft-versus-tumor effect). Sometimes the transplanted cells from a donor can also make an immune response against the body's normal cells. Giving cyclosporine and mycophenolate mofetil after the transplant may stop this from happening. PURPOSE: This phase II trial is studying how well giving chemotherapy and radiation therapy together with rituximab and an umbilical cord blood transplant works in treating patients with B-cell non-Hodgkin's lymphoma.

NCT ID: NCT00387608 Completed - Lymphoma Clinical Trials

ABT-888 in Patients With Refractory Solid Tumors or Hematologic Cancer

Start date: June 2006
Phase: Phase 1
Study type: Interventional

RATIONALE: ABT-888 may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Collecting and storing samples of blood from patients with cancer to study in the laboratory may help doctors learn more about the ways a patient's body handles the drug. PURPOSE: This early phase I trial is studying the side effects and best dose of ABT-888 in patients with refractory solid tumors or hematologic cancer.

NCT ID: NCT00387530 Withdrawn - Lymphoma Clinical Trials

Phenylbutyrate and Valganciclovir in Treating Patients With Relapsed or Refractory Epstein-Barr Virus-Positive Cancer

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

RATIONALE: The Epstein-Barr virus can cause cancer and lymphoproliferative disorders. Valganciclovir is an antiviral drug that acts against the Epstein-Barr virus. Phenylbutyrate may make cells infected with Epstein-Barr virus more sensitive to valganciclovir. Giving phenylbutyrate together with valganciclovir may block the growth of Epstein-Barr virus-infected cells and kill more cancer cells. PURPOSE: This phase II trial is studying how well giving phenylbutyrate together with valganciclovir works in treating patients with relapsed or refractory Epstein-Barr virus-positive cancer.

NCT ID: NCT00387023 Completed - Lymphoma Clinical Trials

Radioimmunotherapy With 90Y Zevalin for Orbital Lymphoma

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

Primary Objectives: 1. To evaluate the efficacy of Zevalin for the treatment of low-grade follicular Non-Hodgkin's lymphoma of the orbit or mucosa-associated lymphoid tissue (MALT) of conjunctiva using radiographic imaging, clinical examination (slit lamp biomicroscopy and external examination of the conjunctiva), and external photography whenever possible. 2. To establish the safety profile in this patient population using clinical examination including slit lamp biomicroscopy, and evaluation of the tear film with Schirmer's test. 3. To establish the dosimetry for Zevalin in the orbit in the first 3 patients who agree to undergo dosimetry.

NCT ID: NCT00386321 Terminated - Clinical trials for Diffuse Large B-cell Lymphoma

Yt90 Zevalin and Combination Chemotherapy (Z-CHOP)in Treating Patients With Stage II, Stage III, or Stage IV Diffuse Large B-cell Lymphoma

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

The purpose of this study is to determine whether the treatment of Yt90 Zevalin in combination with CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisolone)are effective as first line treatment in patients with bulky stage II or stage III or IV diffuse large B-cell lymphoma