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Leukemia clinical trials

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NCT ID: NCT04215822 Not yet recruiting - Clinical trials for Acute Myeloid Leukemia

PHF19 Gene Expression and EZH2 Gene Deletion in Acute Myeloid Leukemia

Start date: January 2020
Phase:
Study type: Observational [Patient Registry]

The study aims to detect pattern of expression of PHF19 gene and EZH2 gene deletion in acute myeloid leukemia patients and detect their prognostic role on patients outcome.

NCT ID: NCT04175587 Not yet recruiting - Clinical trials for Acute Promyelocytic Leukaemia

Randomized,International Multi-center Clinical Trial of RIF Plus RA for Non-high-risk APL

RIF
Start date: December 1, 2019
Phase: Phase 3
Study type: Interventional

Acute Promyelocytic Leukaemia (APL) has been known as a type of cancer, which is of great significance to improve its eradication rate. Recent clinical trials show that ATRA plus ATO treatment regimen can result in complete response (CR) in 90-94% of patients and 5-year disease-free survival (DFS) in more than 90% of patients. However, the ATRA plus ATO treatment regimen can achieve considerate survival rate, patients still need to receive infusion therapy in hospital. If oral arsenic can replace intravenous ATO without reduction of the efficacy, patients would not need to be administered to receive treatment, which would highly increase their quality of lives. Phase I, II Clinical trials have verified the security and efficacy of the Compound Realgar-Indigo Naturalis Formula. Compound Realgar-Indigo Naturalis Formula was approved by the China Food and Drug Administration in 2009. Investergators have done a multi-centre, randomized, controlled, non-inferiority phase 3 clinical trial in China. And the result showed that oral arsenic plus retinoic acid has an anti-leukaemic efficacy similar to the intravenous arsenic treatment. So Investigators performed an international multi-center, Randomized controlled clinical trialsto compare the efficacy of oral RIF plus ATRA with intravenous arsenic trioxide plus ATRA in patients with non-high-risk APL in different racial types.

NCT ID: NCT04168788 Not yet recruiting - Clinical trials for Acute Lymphoblastic Leukemia

Pharmacogenetic Study of Antimitotic Therapies Involved in Hepatic VOD in Children With Nephroblastoma or ALL

MVO
Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Hepatic veno-occlusive diseases (VOD) during cancer treatment in children are serious toxicities that have occurred with interruptions of chemotherapy and risk of relapse. In addition, these toxicities have a negative impact on the patient's quality of life, serious long-term sequelae and are potentially fatal in children. The risk factors associated with the occurrence of these complications are, to date, unknown, at the exception to the exposition to certain treatments (6-thioguanine, busulfan, actinomycin D, radiotherapy, etc.). To understand the effects of this toxicity and those of susceptibility to the disease becomes a major issue in the treatment of these children.

NCT ID: NCT04163575 Not yet recruiting - Lymphoma Clinical Trials

Immunotherapy With CD22 CAR T-cells for B-Cell Lymphoma, ALL and CLL

Start date: February 1, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

This study aims to evaluate the safety, efficacy and duration of response of CD22 Chimeric Antigen Receptor (CAR) redirected autologous T-cells in patients with high risk, relapsed CD22+ haematological malignancies.

NCT ID: NCT04133220 Not yet recruiting - Clinical trials for Leukemia, Myeloid, Acute

Endothelial Activation Hemostasis Disturbances and Severe Bleeding Events in Hyperleukocytic Acute Myeloid Leukemia

HEAL
Start date: October 2019
Phase:
Study type: Observational

Hyper-leukocytosis > 50.109/L is observed in 15% of acute myeloid leukemia (AML). Level of hyper-leukocytosis is linearly associated with the incidence of life threatening complications that lead to the early death in 25% of these patients. The HEAL project is a prospective, uni-centric, observational study that plans to include a cohort of 50 patients presenting de novo AML with hyper-leukocytosis (HL) (> 50.109/L) and 10 controls. The aim of the study is to describe the relative proportion of various hemostasis components disturbances, endothelium alterations, platelet dysfunction and to calculate cumulative incidence of hemorrhagic and thrombotic complications as well as overall survival of patients presenting with HL AML.

NCT ID: NCT04100187 Not yet recruiting - Leukemia Clinical Trials

Immunotherapy With CD19 CAR T-cells for B-Cell Leukemia

Start date: February 1, 2023
Phase: Phase 1
Study type: Interventional

This study aims to evaluate the safety, efficacy and duration of response of CD19 Chimeric Antigen Receptor (CAR) redirected autologous T-cells in patients with high risk, relapsed CD19+ haematological malignancies.

NCT ID: NCT04096846 Not yet recruiting - Clinical trials for Acute Lymphoblastic Leukemia

Effect of Vitamin D Diffiency on Oral Mucosa in Patients Recieving Methotrexate Chemotherapy

VitDandMTX
Start date: November 1, 2019
Phase:
Study type: Observational

it's a prospective study aiming to improve quality of life of patients with acute lymphoblastic leukemia suffering from oral mucositis, receiving courses of methotrexate chemotherapy , by measuring vitamin D in those patients before induction therapy and the change in its level during treatment, that associated with methotrexate-induced oral mucositis, taking in consideration serum level of methotrexate, so we may have assiotiation between vitamin D difficiency and oral mucositis . at the end we can have preventive interventions to protect against this harmful side effect.

NCT ID: NCT04092348 Not yet recruiting - Clinical trials for Acute Lymphoblastic Leukemia

FoxO3a and PU.1 in Acute Lymphoblastic Leukemia

Start date: August 1, 2023
Phase:
Study type: Observational

Acute Lymphoblastic Leukemia (ALL) is one of the four major types of leukemia which is common in both children and adolescents; however, it is the most common pediatric malignancy diagnosed in children younger than 20 years .The disease pathogenesis results from blockade at any stages of normal lymphoid differentiation with uncontrolled proliferation of lymphoid cells. According to the World Health Organization (WHO) definition, ALL is categorized in B-Lymphoblastic Leukemia (B-ALL) And T-Lymphoblastic Leukemia (T-ALL), originated from B- and T-Lineage lymphoid precursor cells, respectively.

NCT ID: NCT04084327 Not yet recruiting - Acute Leukemia Clinical Trials

Immunophenotyping of Acute b Cell Lymphoblstic Leukemia

Start date: September 1, 2019
Phase:
Study type: Observational

To study the immunophenotyping pattern of acute B lymphoblastic leukemia in south Egypt Cancer Institute iand its correlation with disease outcome

NCT ID: NCT03978858 Not yet recruiting - Clinical trials for Leukemia, Myeloid, Acute

A Study of Cusatuzumab Plus Azacitidine in Participants With Newly Diagnosed Acute Myeloid Leukemia Who Are Not Candidates for Intensive Chemotherapy

Start date: June 28, 2019
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the efficacy of cusatuzumab in combination with azacitidine in participants with previously untreated acute myeloid leukemia (AML) who are not eligible for intensive chemotherapy.