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Hematological Malignancies clinical trials

View clinical trials related to Hematological Malignancies.

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NCT ID: NCT02215070 Completed - Clinical trials for Hematological Malignancies

Pasireotide in Prevention of GI Toxicity

Start date: January 21, 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate if the drug, Pasireotide, is safe and effective in reducing the gastrointestinal side effects of the drugs received to prepare for allogeneic stem cell transplant. The study will also evaluate if Pasireotide is effective in reducing acute and chronic Graft-versus-Host-Disease (GvHD) after transplant.

NCT ID: NCT02199548 Completed - Solid Tumor Clinical Trials

The Good Patient Study

Start date: July 2014
Phase: N/A
Study type: Observational

Adolescents with cancer weigh multiple influences in medical decision-making, including their own best interest, the perceived wishes of family members, and the interpreted preferences of the health care team. Parents of children with cancer often describe themselves as trying to be a good parent in making decisions in the child's best interest. Adolescents with cancer often describe themselves as trying to be a good patient and good child in making decisions in accord with how they believe a good patient and good child would decide. Among the challenges of caring for adolescents is the reality that the formative relational influences in adolescents' decision-making are both complex and unique due to adolescent patients' social networks and relational roles. Delineating adolescents' definitions of being a good patient, a good child, a good sibling, and a good friend may enable the care team to better understand the formative decisional influences relevant to adolescents with cancer. Expanding knowledge about the decision making constructs relevant to adolescents with cancer and recognizing the role of these social constructs in medical interactions has the potential for development of a comprehensive care model that methodically evaluates the self-assessed decision making influences and needs of adolescents at various stages in oncology care. This qualitative construct-defining study represents an initial step in the development of enhanced interventions for improved psychosocial support in this vulnerable population.

NCT ID: NCT01916057 Completed - Neutropenia Clinical Trials

Hepatosplenic CANdidiasis : PETscan and Immune Response Analysis

CANHPARI
Start date: November 19, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether F18 fluorodeoxyglucose (18F-FDG) positron-emission tomography scan (PET scan) is useful for the therapy strategy of hepatosplenic candidiasis.

NCT ID: NCT01830010 Completed - Clinical trials for Hematological Malignancies

A Two-part Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of KRP203 in Patients Undergoing Stem Cell Transplant for Hematological Malignancies

Start date: June 28, 2013
Phase: Phase 1
Study type: Interventional

Two part study to evaluate the safety, tolerability, pharmacokinetics, and efficacy (in Part 2 only) of KRP203 in patients undergoing allogeneic hemopoietic stem cell transplant for hematological malignancies

NCT ID: NCT01816230 Completed - Clinical trials for Acute Myeloid Leukemia (AML)

Transplantation of NiCord®, Umbilical Cord Blood-derived Ex Vivo Expanded Cells, in Patients With HM

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

A Study Evaluating the Safety and Efficacy of Transplantation of a single cord blood unit (CBU) of NiCord®, umbilical cord blood-derived Ex Vivo Expanded Stem and Progenitor Cells in Patients with Hematological Malignancies.

NCT ID: NCT01725555 Completed - Solid Tumors Clinical Trials

A Study to Assess the Effect of Food on the Bioavailability of the IGF-1R Inhibitor AXL1717 in Patients With Advanced Malignant Tumors

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

This is a prospective, randomized, open-label, Phase I, crossover study to assess the effect of food on the bioavailability of AXL1717 including patients with advanced malignant tumors

NCT ID: NCT01627275 Completed - Clinical trials for Hematological Malignancies

Naive T-Cell Depleted DLI Following Allo Stem Cell Transplant

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

Allogeneic stem cell transplantation offers the hope of cure for a wide variety of hematologic malignancies. Mature donor T-cells play a critical role in the success or failure of this procedure and a subset of donor T-cells mediate graft-versus-host disease while other subsets provide the foundation for immune recovery. The major challenge in allogeneic stem cell transplantation is determining how to maximally exploit the beneficial effects mediated by T-cells without causing GvHD. This challenge could be overcome by selectively depleting the population of donor T-cells responsible for eliciting the GvHD response. The study hypothesis is depletion of naïve T-cells from the donor lymphocyte inoculum will not cause GVHD while providing T-cells to affect both anti-infection and anti-tumor responses.

NCT ID: NCT01607892 Completed - Clinical trials for Hematological Malignancies

Safety Study of the Selective Inhibitor of Nuclear Export (SINE) KPT-330 in Patients With Advanced Hematological Cancer

Start date: July 23, 2012
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to find out more information relating to the highest dose of KCP-330 that can be given safely and side effects it may cause, to examine how the body affects KCP-330 concentrations in the blood (pharmacokinetics or PK), to examine the effects of KCP-330 on the body (pharmacodynamics or PDn) and to obtain information on its effectiveness in treating cancer.

NCT ID: NCT01349101 Completed - Clinical trials for Hematological Malignancies

A Research Study of Bone Marrow Transplantation From Unrelated or Partially Matched Related Donors

Start date: February 10, 2011
Phase: Phase 2
Study type: Interventional

It is hypothesized that engraftment when administering cyclophosphamide post the stem cell infusion will increase, the incidence of graft versus host disease (GVHD) and day 100 mortality will decrease, and the use of cyclophosphamide post stem cell infusion with alternative donors will be as safe and as effective as traditional matched transplants.

NCT ID: NCT01315132 Completed - Multiple Myeloma Clinical Trials

A Study of Bone Marrow Transplantation Using Fully-Matched Relatives as Donors for Patients With Hematological Malignancies

Start date: April 10, 2008
Phase: Phase 2
Study type: Interventional

This research study uses a drug called cyclophosphamide to decrease the incidence of GVHD in matched sibling hematopoietic stem cell transplant. In doing so, the goal of the study is to increase overall survival.