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Leukemia clinical trials

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NCT ID: NCT00829647 Withdrawn - Leukemia Clinical Trials

A Study Using Two Oral Chemotherapy Agents for Chronic Lymphocytic Leukemia

Start date: January 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Dasatinib and lenalidomide are both prescribed for use in patients with different cancers of the blood. This study is experimental because neither drug has been approved by the Food and Drug Administration for the treatment of chronic lymphocytic leukemia. There are few standard treatments when fludarabine is no longer effective in patients with CLL. Some patients have received additional combination therapy with fludarabine, Campath, bone marrow transplants or supportive care. Dasatinib and lenalidomide have been effective in high-risk CLL patients in other pilot mono therapy studies. The combination of dasatinib and lenalidomide has not been studied in humans before and this study is designed to test whether this combination is safe to use.

NCT ID: NCT00816413 Withdrawn - Lymphoma Clinical Trials

Donor Stem Cell Transplant, Pentostatin, and Total-Body Irradiation in Treating Patients With Hematological Cancer

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

RATIONALE: Giving low doses of chemotherapy and total-body irradiation before a donor peripheral blood stem cell transplant helps stop the growth of cancer cells. It may also stop 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. Removing the T cells from the donor cells before transplant and giving cyclosporine and mycophenolate mofetil after transplant may stop this from happening. PURPOSE: This phase I/II trial is studying the side effects of giving a donor stem cell transplant after pentostatin and total-body irradiation and to see how well it works in treating patients with hematological cancer.

NCT ID: NCT00800566 Withdrawn - Leukemia Clinical Trials

Oral Clofarabine in Chronic Lymphocytic Leukemia (CLL)

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

The goal of this clinical research study is to find the highest tolerable dose of clofarabine when given to patients with CLL. The safety of this drug will also be studied.

NCT ID: NCT00770419 Withdrawn - Depression Clinical Trials

Perceptions of Burden in Patients With Late-Stage Cancer and Their Caregivers

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

RATIONALE: Gathering information over time about patients' sense of being a burden on their caregiver, and caregivers' sense of burden on themselves, may help doctors learn more about the desire to die in patients with late-stage cancer. PURPOSE: This clinical trial is studying perceptions of burden in patients with late-stage cancer and their caregivers.

NCT ID: NCT00758693 Withdrawn - Clinical trials for Chronic Lymphocytic Leukemia

Frontline Treatment With Bendamustine in Combination With Rituximab in Adults Age 65 or Older With Chronic Lymphocytic Leukemia (CLL)

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

Many chemotherapy combinations may be used to treat patients with chronic lymphocytic leukemia (CLL). Although there are many options, a single, best option is not agreed upon by most cancer specialists. Bendamustine, a medicine recently approved for use in the United States, has been used in combination with rituximab in previous studies to treat patients whose CLL has returned after previous standard treatments. The purpose of this study is to determine whether bendamustine with rituximab is effective for the initial treatment of CLL for patients aged 65 and older.

NCT ID: NCT00732186 Withdrawn - Clinical trials for Leukemia, Myeloid, Chronic

Study of Ipilimumab and Dasatinib Combination Therapy in Patients With Chronic or Accelerated Chronic Myeloid Leukemia

Start date: August 2009
Phase: Phase 1
Study type: Interventional

The purpose of the study is to assess the safety of ipilimumab and dasatinib combination therapy in patients with CML

NCT ID: NCT00730652 Withdrawn - Clinical trials for Chronic Lymphocytic Leukemia or Mantle Cell Lymphoma.

Study of MDX-1411 in Patients With Relapsed/Refractory Chronic Lymphocytic Leukemia or Mantle Cell Lymphoma

MDX1411-02
Start date: May 2009
Phase: Phase 1
Study type: Interventional

To determine if MDX-1411 is safe for the treatment of chronic lymphocytic leukemia or mantle cell lymphoma.

NCT ID: NCT00676871 Withdrawn - Clinical trials for Chronic Lymphocytic Leukemia

A Study to Evaluate the Safety, Tolerability, and Antitumor Activity of Continuous Intravenous Infusion of MEDI-538 in Adults With B-Cell Chronic Lymphocytic Leukemia (CLL)

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

Phase 1: - Evaluate the safety and tolerability of MEDI-538 given by escalated doses with continuous IV infusion for 4 weeks in adult patients with CLL. - Determine the maximum tolerated dose (MTD) of MEDI-538 administered by continuous IV infusion for 4 weeks in this patient population - Describe the pharmacokinetics (PK) of MEDI-538 - Describe the immunogenicity (IM) of MEDI-538 - Determine the overall response, which is defined as follows: (1) conversion from PD/SD to PR/nPR/CR or conversion from PR to nPR/CR using standard NCI-WG criteria; or (2) conversion from MRD positivity to MRD negativity using 4-color flow cytometry; and - Describe any antitumor activity (ie, time to response and duration of response) of MEDI-538 in this patient population. Phase 2: - To determine the overall response in adult patients with CLL who have residual disease following previous therapy for CLL. - Describe the safety,PK,and IM of MEDI-538 - Determine the time to MRD relapse - Determine the antitumor activity (ie, time to response, duration of response,and time to progression [TTP])of MEDI-538 in this patient population.

NCT ID: NCT00670150 Withdrawn - Clinical trials for Acute Promyelocytic Leukemia

New Retinoid Agent Combined With Arsenic Trioxide for Untreated Acute Promyelocytic Leukemia

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

The safety and efficacy of combining NRX 195183 with arsenic trioxide in treating untreated APL will be assessed.

NCT ID: NCT00624962 Withdrawn - Leukemia Clinical Trials

Early Enteral Tube Feedings in Children Receiving Chemo for AML/MDS & High Risk Solid Tumors

Start date: March 2006
Phase: N/A
Study type: Interventional

RATIONALE: Tubefeeding may help maintain good nutrition and lessen weight loss in younger patients receiving chemotherapy for cancer. PURPOSE: This clinical trial is studying how well tube feedings work in younger patients receiving chemotherapy for newly diagnosed acute myeloid leukemia, myelodysplastic syndrome, or high-risk solid tumors.