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临床试验/NCT05582083
NCT05582083No Longer Available不适用

Managed Access Program for Momelotinib in Patients With a Diagnosis of Intermediate or High-risk Myelofibrosis (MF), Including Primary Myelofibrosis (PMF) or Secondary Myelofibrosis (Post- Polycythemia Vera/ Essential Thrombocytopenia (PV/ET)), With Anaemia

GlaxoSmithKline0 个研究点开始时间: 2022年10月17日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
No Longer Available

研究概览

简要总结

Compassionate use access to Momelotinib/GSK3070785 for eligible participant with diagnosis of intermediate or high-risk myelofibrosis (MF), including primary myelofibrosis (PMF) or secondary myelofibrosis (post- polycythemia vera/ essential thrombocytopenia (PV/ET)), with anemia.

研究设计

研究类型
Expanded Access

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

  • Written informed consent can be obtained from the patient or legally authorised representative as per local regulations
  • Diagnosis of intermediate or high-risk myelofibrosis (MF), including primary myelofibrosis (PMF) or secondary myelofibrosis (post- polycythemia vera/ essential thrombocytopenia (PV/ET)), with anemia
  • 18 years or older (at the time consent is obtained)
  • The patient is willing to abide by the contraception requirements.
  • No known hypersensitivity to momelotinib, its metabolites, or any of the formulation excipients

排除标准

  • Pregnant or breastfeeding female

研究者

申办方类型
Industry
责任方
Sponsor

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Managed Access Program for Momelotinib in... | 临床试验