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Hematology clinical trials

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NCT ID: NCT03595501 Completed - Hematology Clinical Trials

Analytical and Clinical Performance Testing Plan

Start date: June 20, 2018
Phase:
Study type: Observational

Clinical and analytical tests will be performed based on risk assessment and system specifications to verify that the performance of the investigational device is in accordance with its specifications.

NCT ID: NCT02835937 Completed - Anemia Clinical Trials

Red Blood Cell Transfusion in the Ambulatory Setting: Impact on Home Functional Status

Start date: September 1, 2016
Phase: N/A
Study type: Interventional

Do ambulatory RBC transfusions improve home functional status?

NCT ID: NCT01418846 Completed - Pediatrics Clinical Trials

Determination of Voriconazole Levels in Saliva - Validation in Specific Subsets of Patients

Start date: October 2012
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the intra-saliva penetration of voriconazole in different subpopulations. The goal is to develop, optimize and validate an easy, non-invasive and painless procedure for Therapeutic Drud Monitoring of voriconazole that can be used in children, ambulatory patients and in patients in whom blood drawing is difficult.

NCT ID: NCT01300026 Completed - Cancer Clinical Trials

AMG 319 Lymphoid Malignancy FIH

Start date: April 2011
Phase: Phase 1
Study type: Interventional

This is a multi-center, phase 1, open-label first-in-human study of AMG 319 in subjects with relapsed or refractory lymphoid malignancies. This study consists of two parts. The dose exploration in part 1, studies cohorts of 3 subjects with relapsed or refractory lymphoid malignancies and uses a practical continuous reassessment model [CRM] to guide dose escalation and to define the MTD. The dose expansion in part 2 will enroll 20 subjects with CLL at a dose no higher than the MTD and further explore the safety, PK, and clinical activity of AMG 319 in this patient population.

NCT ID: NCT00472290 Completed - Clinical trials for Myelodysplastic Syndromes

Evaluating the Safety of Long Term Dosing of Romiplostim (Formerly AMG 531) in Thrombocytopenic Subjects With Myelodysplastic Syndromes (MDS)

Start date: April 1, 2007
Phase: N/A
Study type: Interventional

This is an open label extension study of romiplostim for treatment of thrombocytopenia (platelet count ≤ 50 x 10^9/L) in MDS subjects. The study is designed to assess the long-term safety of treatment with romiplostim, as measured by incidence of overall adverse events, the incidence of bleeding events, the utilization of platelet transfusions, and the duration of platelet response. The study will further describe the time to disease progression to acute myeloid leukemia (AML) and survival.

NCT ID: NCT00066092 Completed - Lymphoma Clinical Trials

Pegfilgrastim PBPC Mobilization Study

Start date: April 2003
Phase: Phase 2
Study type: Interventional

This is a randomized, double-blind, multi-center study to assess the safety and effectiveness of using a single subcutaneous (under the skin) injection of pegfilgrastim or daily subcutaneous injections of Filgrastim to mobilize stem cells for autologous transplantation in patients with Hodgkin's or non-Hodgkin's lymphoma.