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临床试验/NCT04932967
NCT04932967已完成不适用

Use of Neutralizing Monoclonal Antibodies for the Treatment of COVID-19 in Patients With Hematological Malignancies (SIE-GIMEMA Study)

Gruppo Italiano Malattie EMatologiche dell'Adulto14 个研究点 分布在 1 个国家目标入组 91 人开始时间: 2021年9月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
91
试验地点
14
主要终点
time to SARS-nCov-2 test negativization

研究概览

简要总结

This is a multicenter retrospective, non-interventional observational study to evaluate the efficacy of nMoAbs in HM patients.

详细描述

This is a multicenter retrospective, non-interventional observational study. The participating centres will retrospectively review all episodes of SARS-CoV-2 infection occurring in HMs identified at their institutions from February 2020 to May 2021 and treated with nMoAbs, to evaluate their efficacy.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All patients must meet all the following criteria for study entry:
  • Age equal to or greater than 18 years of age.
  • Diagnosis of HM (acute leukemias, myelodysplastic syndromes, myeloproliferative neoplasms, lymphomas, myeloma, chronic myeloprolipherative disorders) at any stage/status.
  • Third generation rapid molecular or antigen test positive for SARS-CoV-2 from February 2020 until May 2021
  • Treatment with anti SARS CoV 2 nMoAbs approved by AIFA
  • Not hospitalized for COVID-19 at the time of nMoAbs administration
  • Not on oxygen therapy at the time of nMoAbs administration
  • At least one of the following symptoms for no more than 10 days:
  • Ageusia / dysgeusia
  • Pharyngodynia
  • Tachypnea
  • Signed written informed consent according to ICH/EU/GCP and national local laws (if applicable).

排除标准

  • Hematological diseases, other than HM.
  • Not tested positive for SARS-CoV-2
  • Patients in disease remission "off therapy" for more than 6 months
  • Immune plasma treatment in the previous two months

结局指标

主要结局

time to SARS-nCov-2 test negativization

时间窗: 3 months

To assess the efficacy of nMoAbs in infected HM patients compared to the historical control

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (14)

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