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Leukemia clinical trials

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NCT ID: NCT01802333 Completed - Clinical trials for Acute Myeloid Leukemia

Cytarabine and Daunorubicin Hydrochloride or Idarubicin and Cytarabine With or Without Vorinostat in Treating Younger Patients With Previously Untreated Acute Myeloid Leukemia

Start date: February 12, 2013
Phase: Phase 3
Study type: Interventional

This randomized phase III trial studies cytarabine and daunorubicin hydrochloride or idarubicin and cytarabine with or without vorinostat to see how well they work in treating younger patients with previously untreated acute myeloid leukemia. Drugs used in chemotherapy, such as cytarabine, daunorubicin hydrochloride, idarubicin, and vorinostat, work in different ways to stop the growth of cancer cells, either by killing the cells, stopping them from dividing, or by stopping from spreading. Giving more than one drug (combination chemotherapy) and giving the drugs in different doses and in different combinations may kill more cancer cells. It is not yet known which combination chemotherapy is more effective in treating acute myeloid leukemia.

NCT ID: NCT01798901 Completed - Clinical trials for Recurrent Adult Acute Myeloid Leukemia

AR-42 and Decitabine in Treating Patients With Acute Myeloid Leukemia

Start date: September 17, 2013
Phase: Phase 1
Study type: Interventional

This phase I trial studies the side effects and best dose of AR-42 when given together with decitabine in treating patients with acute myeloid leukemia. AR-42 may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as decitabine, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving AR-42 together with decitabine may kill more cancer cells.

NCT ID: NCT01795716 Completed - Clinical trials for Chronic Myeloid Leukemia

Bioequivalence Study of Mesylate Imatinib Capsule in Chronic Myeloid Leukemia Body

Start date: September 2012
Phase: Phase 1
Study type: Interventional

1. purpose: To conduct the relative bioavailability study of a single dose and multiple doses of imatinib mesylate capsule (Jiangsu Chia-Tai Tianqing Pharmacy Co. Ltd.) versus Glivec (Novartis Pharma Stein AG). 2. Experimental Design: Two-period crossover design 3. Test drug: imatinib mesylate capsule Reference drug: Glivec 4. Sample size:20

NCT ID: NCT01795378 Completed - Clinical trials for Acute Lymphoblastic Leukemia

Safety and Efficacy Study of Donor Natural Killer Cells Given After Haploidentical Hematopoietic Cell Transplantation

DNKI-II
Start date: February 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The protocol treatment is to evaluate clinical effects of donor-derived natural killer cells that are given after HLA-mismatched hematopoietic cell transplantation.

NCT ID: NCT01794702 Completed - Leukemia Clinical Trials

Decitabine Followed by Clofarabine, Idarubicin, and Cytarabine in Acute Leukemia

Start date: February 20, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The goal of Phase I of this clinical research study is find the highest tolerable dose of clofarabine that can be given with decitabine, idarubicin, and cytarabine to patients with acute leukemia. The goal of Phase II of this study is to learn if decitabine followed by the combination of clofarabine, idarubicin, and cytarabine can help to control acute leukemia. The safety of this drug combination will also be studied. Decitabine and idarubicin are designed to damage the DNA (the genetic material of cells). This may cause cancer cells to die. Clofarabine is designed to interfere with the growth and development of cancer cells. Cytarabine is designed to insert itself into DNA and stop the DNA from repairing itself.

NCT ID: NCT01794299 Completed - Clinical trials for Acute Myeloid Leukemia

Safety and Efficacy of Donor T-lymphocytes Depleted ex Vivo of Host Alloreactive T-cells (ATIR) in Patients With a Hematologic Malignancy Who Received a Hematopoietic Stem Cell Transplantation From a Haploidentical Donor

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

The purpose of this study is to determine whether ATIR is safe and effective in reducing transplant-related mortality and improving overall survival, when infused in patients with a hematologic malignancy following a T-cell depleted stem cell graft from a related haploidentical donor.

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: NCT01787474 Completed - Clinical trials for Recurrent Adult Acute Myeloid Leukemia

Donor Natural Killer Cells in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia

Start date: May 19, 2014
Phase: Phase 1
Study type: Interventional

This phase I/II trial studies the side effects and best dose of donor natural kill cells and to see how well they work in treating patients with acute myeloid leukemia that does not respond to treatment (refractory) or has come back after a period of improvement (relapsed). Giving natural killer cells after high dose chemotherapy may boost the patient's immune system by helping it see the remaining cancer cells as not belonging in the patient's body and causing it to destroy them (called graft-versus-tumor effect).

NCT ID: NCT01786343 Completed - Leukemia Clinical Trials

Decitabine for Older or Unfit Patients With Acute Myeloid Leukemia (AML)

Start date: February 5, 2013
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to compare how well 2 different dosing schedules of decitabine may help control AML. Decitabine is designed to damage the DNA (the genetic material) of cells, which may cause cancer cells to die.

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).