Myeloproliferative Neoplasms Clinical Trial
Long-term Safety and Efficacy of Momelotinib in Subjects With Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, Post-essential Thrombocythemia Myelofibrosis, Polycythemia Vera or Essential Thrombocythemia
Summary
This open-label study is to determine the long-term safety and tolerability of momelotinib in previously enrolled study participants with primary myelofibrosis (PMF), post-polycythemia vera myelofibrosis (post-PV MF), post-essential thrombocythemia myelofibrosis (post-ET MF), polycythemia vera (PV), or essential thrombocythemia (ET), who have tolerated and achieved stable disease or better with momelotinib treatment while enrolled in a previous clinical trial.
Eligibility Criteria
Key Inclusion Criteria:
Currently enrolled in study CCL09101E, or YM387-II-02, or successfully completed 24 weeks of study GS-US-352-1672
Able to comprehend and willing to sign informed consent form
Key Exclusion Criteria:
Known hypersensitivity to momelotinib, its metabolites, or formulation excipients
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
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There is 1 Location for this study
Scottsdale Arizona, , United States
Orange California, , United States
Stanford California, , United States
Whittier California, , United States
Jacksonville Florida, , United States
Baltimore Maryland, , United States
Boston Massachusetts, , United States
Ann Arbor Michigan, , United States
Rochester Minnesota, , United States
Saint Louis Missouri, , United States
Bronx New York, , United States
New York New York, , United States
Cleveland Ohio, , United States
Houston Texas, , United States
Salt Lake City Utah, , United States
Frankston Victoria, , Australia
Parkville Victoria, , Australia
Toronto Ontario, , Canada
Montreal Quebec, , Canada
La Tronche , , France
Paris , , France
Minden , , Germany
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