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Leukemia clinical trials

View clinical trials related to Leukemia.

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NCT ID: NCT01736943 Completed - Clinical trials for Acute Myelogenous Leukemia

Bortezomib and Doxil for the Treatment of Patients With Acute Myelogenous Leukemia

Start date: December 19, 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether bortezomib in combination with doxil/lipodox is effective in the treatment of Acute Myeloid Leukemia.

NCT ID: NCT01736683 Completed - Anemia Clinical Trials

Study of Sotatercept for the Treatment of Anemia in low-or Intermediate-1 Risk Myelodysplastic Syndromes (MDS) or Non-proliferative Chronic Myelomonocytic Leukemia (CMML)

Start date: November 28, 2012
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to determine a safe, tolerable and effective dose of sotatercept that results in the greatest frequency of improvement of anemia in patients diagnosed with low- or intermediate-1 risk myelodysplastic syndromes (MDS) or non-proliferative chronic myelomonocytic leukemia (CMML).

NCT ID: NCT01735955 Completed - Clinical trials for Acute Lymphoblastic Leukemia (ALL)

Study to Allow Access to Nilotinib for Patients Who Are on Nilotinib Treatment in a Novartis-sponsored Study

Start date: March 29, 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study was to allow continued use of nilotinib in patients who were on nilotinib treatment in a Novartis-sponsored, Oncology Clinical Development & Medical Affairs (CD&MA) study and were benefiting from the treatment as judged by the investigator

NCT ID: NCT01735604 Recruiting - Clinical trials for Recurrent Mantle Cell Lymphoma

Genetically Engineered Lymphocyte Therapy in Treating Patients With Lymphoma That is Resistant or Refractory to Chemotherapy

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

RATIONALE: Placing a gene that has been created in the laboratory into white blood cells may make the body build an immune response to kill cancer cells. PURPOSE: This clinical trial is studying genetically engineered lymphocyte therapy in treating patients with B-cell leukemia or lymphoma that is resistant or refractory to chemotherapy.

NCT ID: NCT01734304 Completed - Clinical trials for Acute Myeloid Leukemia

DC Vaccination for Postremission Therapy in AML

Start date: November 5, 2013
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to determine the feasibility and safety of an autologous DC immunotherapy in patients with AML of non-favorable risk profile.

NCT ID: NCT01732861 Completed - Clinical trials for Leukemia Lymphocytic Chronic B-Cell

Safety Study of CC-292 and Lenalidomide in Subjects With Chronic Lymphocytic Leukemia/ Small Lymphocytic Lymphoma

Start date: December 28, 2012
Phase: Phase 1
Study type: Interventional

This is a dose finding study using a 3 + 3 dose escalation and expansion design to determine a Not Tolerated Dose (NTD), Optimal Biological Effect Dose (OBE) and / or Maximum Tolerated Dose (MTD). These data will be used to establish a Recommended Phase 2 Dose (RP2D) for the combination of CC-292 and lenalidomide in subjects with Chronic Lymphocytic Leukemia (CLL).

NCT ID: NCT01729845 Completed - Clinical trials for Recurrent Adult Acute Myeloid Leukemia

Decitabine Followed by Mitoxantrone Hydrochloride, Etoposide, and Cytarabine in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia or High-Risk Myelodysplastic Syndromes

Start date: December 20, 2012
Phase: Phase 1/Phase 2
Study type: Interventional

This phase I/II trial studies the side effects and best dose of decitabine followed by mitoxantrone hydrochloride, etoposide, and cytarabine and to see how well they work in treating patients with acute myeloid leukemia or high-risk myelodysplastic syndrome that has returned after a period of improvement or does not respond to treatment. Drugs used in chemotherapy, such as mitoxantrone hydrochloride, etoposide, cytarabine, and decitabine, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving more than one drug (combination chemotherapy) may kill more cancer cells.

NCT ID: NCT01728402 Enrolling by invitation - Clinical trials for Myelodysplastic Syndromes

Pathogenesis of Hematologic Malignancies

Start date: September 2008
Phase:
Study type: Observational

The cause of blood and bone marrow cancers is poorly understood; however, most research focuses on how cancer cells grow and develop. Because the causes of these cancers are unknown, current treatments may be unnecessarily harsh and often do not provide a cure. Identifying the causes of blood cancers would allow for the development of treatments that are more likely to provide a cure. To find the causes of blood and bone marrow cancers, we will look for specific cancer cell abnormalities that are responsible for cancer cell growth. We will then look to see if drugs that can reverse these abnormalities can kill cancer cells.

NCT ID: NCT01728389 Recruiting - Lymphoma Clinical Trials

Intrabone Transplantation of Allogenic Peripheral Blood Stem Cells in Patients With Myeloid and Lymphoid Malignancies.

Start date: November 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is to evaluate efficacy and safety of direct intrabone transplantation procedure of peripheral blood haematopoietic stem cells form HLA-matched sibling donors in patients with myeloid and lymphoid malignancies.

NCT ID: NCT01728207 Terminated - Clinical trials for Chronic Lymphocytic Leukemia

Phase I Dose Escalation Study of IMMU-114 in Relapsed or Refractory NHL and CLL

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

IMMU-114 will be studied at different dose schedules and dose levels in order to assess the highest dose safely tolerated. IMMU-114 will be administered subcutaneously (under the skin). IMMU-114 will be given 1-2 times weekly for 3 weeks followed by one week of rest. This is considered one cycle. Treatment cycles will be repeated until toxicity or worsening of disease.