Паровичникова Елена Николаевна


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IMPACT-AML ClinicalTrials.gov

Статус: Recruiting
Фаза: Phase 3
Начало: 1 апреля 2024 г.
Окончание: 1 мая 2029 г.
Описание: The primary objective is to evaluate the efficacy and toxicity of high versus low intensity therapy options in patients with refractory forms and early relapses of acute myeloid leukemia (R/R AML) who are scheduled for allogeneic hematopoietic stem cell transplantation (alloHSCT).
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RALL-2016m ClinicalTrials.gov

Статус: Recruiting
Фаза: N/A
Начало: 1 апреля 2023 г.
Окончание: 1 сентября 2027 г.
Описание: Non-intensive But Non-interruptive Treatment based on previously study RALL-2016 of Adult Ph-negative Acute Lymphoblastic Leukemia: No high-dose methotrexate (MTX) and high-dose cytarabine (ARA-C) consolidation blocks, L-asparaginaseis scheduled for 1 year of treatment, 21 intrathecal injections through the whole treament, T-ALL patients in complete remission (CR) with MRD-positive status after 2nd induction receive consolidation 1-3 with venetoclax (56 days), and B-ALL patients in complete remission (CR) with MRD-positive status after 2nd induction receive 1 consolidation with blinatumomab. After that consolidation bone samples are collected and tested for MRD and patients will continue therapy by protocol without HSCT if MRD-negative (by flow cytometry by aberrant immunophenotype in a centralized lab) status was achieved.
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PMBL-2022 ClinicalTrials.gov

Статус: Recruiting
Фаза: Phase 3
Начало: 1 апреля 2022 г.
Окончание: 1 апреля 2029 г.
Описание: This compares the effects of nivolumab at a fixed dose of 40 mg with chemo-immunotherapy versus chemo-immunotherapy alone in treating patients with newly diagnosed primary mediastinal B-cell lymphoma (PMBCL). Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of cancer cells to grow and spread. Treatment for PMBCL involves chemotherapy combined with an immunotherapy called rituximab. Chemotherapy drugs 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. Rituximab is a monoclonal antibody. It binds to a protein called CD20, which is found on B cells (a type of white blood cell) and some types of cancer cells. This may help the immune system kill cancer cells. Giving nivolumab with chemo-immunotherapy may help treat patients with PMBCL.
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R/r cHL-2022 ClinicalTrials.gov

Статус: Recruiting
Фаза: Phase 2
Начало: 19 августа 2019 г.
Окончание: 1 марта 2025 г.
Описание: Nivolumab is an anti-PD-1 antibody highly effective in patients with relapsed/refractory classical Hodgkin lymphoma. A PET-adapted regimen of nivolumab combined with salvage therapy was shown to induce high response rates and favorable progression-free survival as a bridge to autologous stem cell transplantation, allowing to omit salvage chemotherapy in a substantial proportion of r\r cHL patients. This study evaluates the safety and efficacy of PET-adapted treatment of nivolumab at the 3 mg/kg in combination with Bendamustine, Gemcitabine, Vinorelbine (Nivo-BeGEV) in patients with relapsed/refractory Hodgkin Lymphoma.
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HGBL DH and HGBL NOS ClinicalTrials.gov

Статус: Unknown status
Фаза: Phase 3
Начало: 15 марта 2018 г.
Окончание: 15 марта 2024 г.
Описание: Purpose: to evaluate an efficacy of chemotherapy regimens R-DA-EPOCH-21 and R-BL-04 with and without autologous hematopoietic stem cells transplantation (auto-SCT) in newly diagnosed patients with High-Grade B-cell Lymphoma Double-hit and High-Grade B-cell Lymphoma Not Otherwise Specified.
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ALL--2016 ClinicalTrials.gov

Статус: Unknown status
Фаза: N/A
Начало: 1 января 2017 г.
Окончание: 1 декабря 2022 г.
Описание: No high-dose methotrexate (MTX) and high-dose cytarabine (ARA-C) consolidation blocks, L-asparaginaseis scheduled for 1 year of treatment, 21 intrathecal injections through the whole treament, T-ALL patients in complete remossion (CR) after the informed consent are randomized to: auto-HSCT vs no auto-HSCT, - with the similar further maintenance. Stem cell harvest is performed after the 3rd consolidation by G-SCF disregarding minimal residual disease (MRD) level. Auto-HSCT is planned after the 5th consolidation phase. All primary bone samples are collected and tested for cytogenetics and molecular markers, all included patients are monitored by flow cytometry by aberrant immunophenotype in a centralized lab.
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BM-MSC-01 ClinicalTrials.gov

Статус: Unknown status
Фаза: Phase 3
Начало: 1 января 2017 г.
Окончание: 31 декабря 2022 г.
Описание: Multipotent mesenchymal stromal cells (MSCs) participate in the formation of bone marrow niches for hematopoietic stem cells. Donor MSCs can serve as a source of recovery for niches in patients with graft failure (GF) after allogeneic bone marrow (BM) transplantation. Since only few MSCs reach the BM after intravenous injection, MSCs were implanted into the iliac spine. Preliminary results suggest that MSCs participate in the restoration of niches for donor hematopoietic cells or have an immunomodulatory effect, preventing repeated rejection of the graft. Perhaps intraosseous implantation of MSCs contributes to the success of the second transplantation of hematopoietic stem cells and patient survival.
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DLBCL-2015 ClinicalTrials.gov

Статус: Unknown status
Фаза: Phase 3
Начало: 1 февраля 2015 г.
Окончание: 1 февраля 2023 г.
Описание: Purpose: to evaluate an efficacy of chemotherapy regimens R-DA-EPOCH-21 and R-mNHL-BFM-90 with and without autologous hematopoietic stem cells transplantation (auto-SCT) in newly diagnosed patients with DLBCL with intermediate and high risk.
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MSC-CY-Russia ClinicalTrials.gov

Статус: Unknown status
Фаза: Phase 2/Phase 3
Начало: 1 января 2014 г.
Окончание: 1 января 2016 г.
Описание: Evaluating the effectiveness of the new protocol which replace the standard immunosuppressive therapy with use of MSCs and CY in patients at high risk of relapse.
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NRCH-MSC ClinicalTrials.gov

Статус: Unknown status
Фаза: Phase 2
Начало: 1 октября 2007 г.
Окончание: 1 октября 2014 г.
Описание: Infusion of Mesenchymal Stem Cell (MSC) at day of recovery after bone marrow transplant (BMT) for patients with AL, AA and MM for acute Graft-versus-host Disease (GVHD) prophylaxis and treatment.
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