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Leukemia clinical trials

View clinical trials related to Leukemia.

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NCT ID: NCT04679506 Not yet recruiting - Clinical trials for Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

the Efficacy and Safety of CLAE in R/R T-ALL/LBL

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

To evaluate the efficacy and safety of CLAE regimen (cladribine + cytarabine + etoposide) in the treatment of relapsed/refractory T-ALL/LBL.

NCT ID: NCT04677231 Not yet recruiting - Clinical trials for Acute Lymphoblastic Leukemia

Evaluation of Long-term Health Status and Quality of Life in Adult Survivors With Philadelphia-negative Acute Lymphoblastic Leukemia/Lymphoma Treated With an Intensive Pediatric or Pediatric-inspired Protocol

EQUAALL01
Start date: January 2021
Phase:
Study type: Observational

The overall survival of adult patients (15-59y) with Philadelphia-negative acute lymphoblastic leukemia/lymphoma (ALL/LL) was dramatically improved by the use of full pediatric or pediatric-inspired protocols (GRAALL2003/05-LL03-FRALLE2000) that aimed to reduce the risk of relapse by adopting more intensive chemotherapeutical schedule. This approach led to a global improvement in overall survival (5y-OS, 57%) whatever patient age but was responsible for an excess of treatment-related mortality in patients older than 45 years (5y-TRM in patients > 45y, 19%). Pediatric longitudinal studies pointed out that long term leukemia survivors have an increased risk of developing specific adverse events like dysmetabolic syndrome, obesity, decreased fertility, organ dysfunction, osseous events, or impaired cognitive functions. This study aims to evaluate the impact in term of long-term events and QoL in adult patients that received an intensified therapeutic approach recently implemented in adult cooperative groups. The main objective of this study is to evaluate the prevalence of late effects in adult patients treated 10 years ago for ALL/LL with an intensified pediatric-inspired protocol (GRAALL2003/05-LL03-FRALLE2000) that exposed patients to increased cumulative doses of chemotherapy, central nervous system irradiation or w/o allogeneic transplant after total body irradiation-based regimen w/o boost irradiation on central nevous system. One of the secondary endpoint of the study is to assess quality of life of these patients.

NCT ID: NCT04658004 Not yet recruiting - Clinical trials for Acute Myeloid Leukemia

NKG2D CAR-T Cell Therapy for Patients With Relapsed and/or Refractory Acute Myeloid Leukemia

Start date: January 15, 2021
Phase: Early Phase 1
Study type: Interventional

A Study of NKG2D CAR-T Cell Therapy for Patients With Relapsed and/or Refractory Acute Myeloid Leukemia.

NCT ID: NCT04653493 Not yet recruiting - Clinical trials for Relapsed B Cell Acute Lymphoblastic Leukemia (ALL)

CD19 Targeted CAR T Cell Therapy in Patients With Relapsed/ Refractory B Cell Acute Lymphoblastic Leukaemia (ALL)

Start date: August 2021
Phase: Phase 1
Study type: Interventional

This is a single-arm, open-label, phase I study (safety and dose escalation) of autologous Chimeric Antigen Receptor (CAR) T-cells targeting CD19 in patients with relapsed/refractory B cell acute lymphoblastic leukemia (ALL).

NCT ID: NCT04609241 Not yet recruiting - Clinical trials for Relapsed and/or Refractory Acute Lymphoblastic Leukemia

CD79b CAR-T Cell Therapy for Patients With Relapsed and/or Refractory Acute Lymphoblastic Leukemia and B-cell Non-Hodgkin's Lymphoma

Start date: November 15, 2020
Phase: Early Phase 1
Study type: Interventional

A study of CD79b CAR-T Cell Therapy for Patients With Relapsed and/or Refractory Acute Lymphoblastic Leukemia and B-cell Non-Hodgkin's Lymphoma

NCT ID: NCT04599543 Not yet recruiting - Clinical trials for Acute Myeloid Leukemia

IL3 CAR-T Cell Therapy for Patients With CD123 Positive Relapsed and/or Refractory Acute Myeloid Leukemia

Start date: November 15, 2020
Phase: Early Phase 1
Study type: Interventional

A Study of IL3 CAR-T Cell Therapy for Patients With CD123 Positive Relapsed and/or Refractory Acute Myeloid Leukemia.

NCT ID: NCT04595162 Not yet recruiting - Clinical trials for B-cell Acute Lymphoblastic Leukemia

A Study of GC019F CAR-T Cell Immunotherapy for Relapsed or Refractory B- ALL

Start date: March 15, 2021
Phase: Phase 1
Study type: Interventional

The study is an early, open, single-centered trial. The aim of this study is to evaluate the safety and tolerance of GC019F CAR-T cell immunotherapy in relapsed or refractory B-ALL. The study will include 6-12 subjects to receive GC019F therapy.

NCT ID: NCT04554381 Not yet recruiting - Clinical trials for Acute Lymphoblastic Leukemia

Assesment of JL1 Expression in Acute Leukemia

Start date: October 13, 2020
Phase: Phase 1
Study type: Interventional

The aim of this study is to assess JL1 expression by flow cytometric immunophenotyping in patients with B-cell Acute Lymphoblastic Leukemia (ALL) and to correlate it with clinical, morphological, immunophenotypic, cytogenetic data and response to treatment.

NCT ID: NCT04497701 Not yet recruiting - Lymphoma Clinical Trials

Evaluate the Efficacy and Safety of the Prophylactic Use of PEG-rhG-CSF in Children With Hematological Malignancies

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

The incidence of infectious complications in hematological malignancies is higher than that in children with solid tumors, which may be related to the type and dose intensity of chemotherapy regimens used in hematological tumors. The treatment of childhood cancer has changed in the past few decades: intensive treatment and good supportive treatment can improve the 5-year survival rate of children. The aim of this study was to evaluate the efficacy and safety of prophylactic use of pegylated recombinant human granulocyte colony-stimulating factor (PEG-rhG-CSF) after chemotherapy in children with hematological malignancies.

NCT ID: NCT04488237 Not yet recruiting - Clinical trials for Acute Lymphoblastic Leukemia

Vitamin D and Methotrexate Adverse Effects

Start date: September 2020
Phase:
Study type: Observational

Since methotrexate toxicity represents a major problem in patients treating with cancer and there are few studies about the role of vitamin D in the pathogenesis of this toxicity, so the aim of the present study is investigation of the effect of vitamin D administration on methotrexate toxicity such as oral ulcerations, bone marrow toxicity as well as renal and hepatic toxicity also the role of inflammatory mediators and oxidative stress markers in methotrexate toxicity will be evaluated, taking in consideration the dose of leucovorin rescue.