Official Title
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
Brief Summary

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.

Available
Individual Patients
Myelofibrosis

Drug: Momelotinib
Momelitinib available as tablets.
Other Name: GSK3070785

Eligibility Criteria

Inclusion Criteria: - 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

Exclusion Criteria: - Pregnant or breastfeeding female

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years
Contacts

US GSK Clinical Trials Call Center
877-379-3718
GSKClinicalSupportHD@gsk.com

EU GSK Clinical Trials Call Center
+44 (0) 20 89904466
GSKClinicalSupportHD@gsk.com

GSK Clinical Trials
Study Director
GlaxoSmithKline

GlaxoSmithKline
NCT Number
Keywords
Momelotinib
GSK3070785
MeSH Terms
Primary Myelofibrosis
N-(cyanomethyl)-4-(2-((4-(4-morpholinyl)phenyl)amino)-4-pyrimidinyl)benzamide