跳至主要内容
临床试验/NL-OMON37318
NL-OMON37318已完成2 期

A single arm, phase II, open-label study to determine the efficacy of 100mg twice daily oral dosing of Midostaurin administered to patients with Agressive Systemic Mastocytosis or Mast Cell Leukemia +/- an Associated Hematological Clonal Non-Mast Cell Lineage Disease - AgressiveSystemicMastocytosis (ASM) or MastCell Leukemia (MCL), midostaurin

ovartis0 个研究点目标入组 3 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
ovartis
入组人数
3

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Adult patients with diagnosis of one major plus at least one minor criterion, or the presence of at least 3 minor criteria according to WHO criteria for Systemic Mastocytosis (Valent et al. 2001);Patient must present with at least one measurable C-Finding.;For patients with MCL: bone marrow aspirate smears must show 20% or more immature mast cells.

排除标准

  • Patients who have demonstrated relapse to more than two prior regimen of SM treatment-regardless of treatment regimen for supportive care (e.g. symptom limiting therapies);Patients who have aggressive systemic mastocytosis with eosinophilia and known positivity for the FIP1L1-PDGFR fusion unless they have demonstrated relapse or disease progression on prior imatinib therapy;Patients on imatinib therapy and known to be KIT D816V negative unless they have demonstrated relapse, resistance or intolerance to imatinib.;Patients with any pulmonary infiltrate including those suspected to be of infectious origin.

研究者

发起方
ovartis

相似试验

进行中(未招募)
1 期
A phase II study to determine if the drug midostaurin taken orally twice daily is effective and safe in treating patients with Agressive Systemic Mastocytosis or Mast Cell Leukemia +/- an associated hematological clonal non-mast cell lineage diseaseAggressive Systemic Mastocytosis or Mast Cell Leukemia +/- an Associated Hematological Clonal Non-Mast Cell Lineage DiseaseMedDRA version: 18.1Level: LLTClassification code 10056453Term: Aggressive systemic mastocytosisSystem Organ Class: 100000004851
EUCTR2008-000280-42-DEovartis Pharma Services AG80
进行中(未招募)
1 期
A single arm, Phase II, Open-label Study to determine the efficacy of 100 mg twice daily oral dosing of midostaurin administered to patients with Agressive Systemic Mastocytosis or Mast Cell Leukemia +/- an associated hematological clonal non-mast cell lineage disease - CPKC412D2201Agressive Systemic Mastocytosis (ASM) or Mast Cell Leukemia (MCL) +/- an Associated Hematological Clonal Non-Mast Cell Lineage Disease (AHNMD)MedDRA version: 9.1Level: LLTClassification code 10056453Term: Aggressive systemic mastocytosis
EUCTR2008-000280-42-FRovartis Pharma Services AG60
进行中(未招募)
1 期
A phase II study to determine if the drug midostaurin taken orally twice daily is effective and safe in treating patients with Agressive Systemic Mastocytosis or Mast Cell Leukemia +/- an associated hematological clonal non-mast cell lineage diseaseAggressive Systemic Mastocytosis or Mast Cell Leukemia +/- an Associated Hematological Clonal Non-Mast Cell Lineage DiseaseMedDRA version: 19.1Level: LLTClassification code 10056453Term: Aggressive systemic mastocytosisSystem Organ Class: 100000004851
EUCTR2008-000280-42-NLovartis Pharma Services AG116
进行中(未招募)
1 期
A phase II study to determine if the drug midostaurin taken orally twicedaily is effective and safe in treating patients with Agressive SystemicMastocytosis or Mast Cell Leukemia +/- an associated hematological clonalnon-mast cell lineage disease
EUCTR2008-000280-42-NOovartis Pharma Services AG116
进行中(未招募)
1 期
A Phase II study to determine if the drug midostaurin taken orally twice daily is effective and safe in treating patients with Agressive Systemic Mastocytosis or Mast Cell Leukemia +/- and associated hematological clonal non-mast cell lineage diseaseAggressive Systemic Mastocytosis or Mast Cell Leukemia +/- an Associated Hematological Clonal Non-Mast Cell Lineage DiseaseMedDRA version: 19.1 Level: LLT Classification code 10056453 Term: Aggressive systemic mastocytosis System Organ Class: 100000004851
EUCTR2008-000280-42-GBovartis Pharma Services AG116
A single arm, phase II, open-label study to... | 临床试验