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
| Status: | Completed |
|---|---|
| Conditions: | Cancer, Cancer, Blood Cancer, Hematology, Hematology |
| Therapuetic Areas: | Hematology, Oncology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 2/6/2019 |
| Start Date: | April 30, 2014 |
| End Date: | December 6, 2018 |
Open-label Study to Assess the 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
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.
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.
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.
We found this trial at
16
sites
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