Found 23 matching trials
Fedratinib in Combination With Nivolumab PHASE2 A multicenter, open-label, single arm, phase II study investigating the cli...
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Universitätsklinikum Freiburg
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A Dose-escalation Study of the Safety and Tolerability of Orally Administered TG101348 in Patients With Myelofibrosis PHASE1 The purpose of this study is to evaluate the safety and tolerability of ora...
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UCSD Moores Cancer Center
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Phase 2 Study in Japanese Patients With Intermediate-2 or High Risk Primary Myelofibrosis, Post-Polycythemia Vera Myelofibrosis, Post-Essential Thrombocythemia Myelofibrosis With Splenomegaly PHASE2 Primary Objective:
\- To evaluate the efficacy of daily oral doses of 300 ...
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Investigational Site Number 392010
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Phase 2 Study of SAR302503 in Patients With Myelofibrosis PHASE2 Primary Objective:
\- To evaluate the efficacy of daily oral doses of 300 ...
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Investigational Site Number 840001
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A Study to Evaluate Single Agent Selinexor Versus Physician's Choice in Participants With Previously Treated Myelofibrosis PHASE2 This is a Phase 2, multicenter, two-arm, open-label study to evaluate the s...
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Active Not Recruiting
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The Oncology Institute of Hope and Innovation
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A Study to Evaluate the Bioavailability of Fedratinib When Administered in Different Ways to Healthy Adult Participants PHASE1 The purpose of this study is to evaluate the relative bioavailability of fe...
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Syneos Health Clinical Research Services, Llc
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A Long-Term Study of the Effects of Orally Administered SAR302503 in Patients With Myelofibrosis PHASE1 The purpose of this study is to evaluate the long-term effects of orally ad...
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Investigational Site Number 840103
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Phase III Study of SAR302503 in Intermediate-2 and High Risk Patients With Myelofibrosis PHASE3 Primary Objective:
* To evaluate the efficacy of daily oral doses of 400 m...
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Investigational Site Number 840014
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Individual Patient Compassionate Use of Fedratinib N/A This is an expanded access program (EAP) for eligible participants designed...
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Drug Interaction Study of SAR302503 in Patients With Solid Tumor PHASE1 Primary Objective:
* To assess the effect of 15-day repeated oral doses of...
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Investigational Site Number 840004
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