Found 12 matching trials
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 ...
Show More Location
Investigational Site Number 392010
Learn More & Join Trial
Phase 2 Study of SAR302503 in Patients With Myelofibrosis PHASE2 Primary Objective:
\- To evaluate the efficacy of daily oral doses of 300 ...
Show More Location
Investigational Site Number 840001
Learn More & Join Trial
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...
Show More Location
Investigational Site Number 840103
Learn More & Join Trial
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...
Show More Location
Investigational Site Number 840014
Learn More & Join Trial
Individual Patient Compassionate Use of Fedratinib N/A This is an expanded access program (EAP) for eligible participants designed...
Show More Learn More & Join Trial
Drug Interaction Study of SAR302503 in Patients With Solid Tumor PHASE1 Primary Objective:
* To assess the effect of 15-day repeated oral doses of...
Show More Location
Investigational Site Number 840004
Learn More & Join Trial
Effect of SAR302503 on ECG Activity in Patients With Solid Tumors PHASE1 Primary Objective:
\- To assess the effect of SAR302503 (500 mg) administe...
Show More Location
Investigational Site Number 840003
Learn More & Join Trial
Phase II, Open Label, Single Arm Study of SAR302503 In Myelofibrosis Patients Previously Treated With Ruxolitinib PHASE2 Primary Objective:
\- To evaluate the efficacy of once daily dose of SAR30...
Show More Location
Investigational Site Number 840007
Learn More & Join Trial
Study With SAR302503 in Patients With Polycythemia Vera or Essential Thrombocythemia PHASE2 Primary Objective:
* Dose Ranging Phase: To evaluate the efficacy of daily...
Show More Location
Investigational Site Number 840008
Learn More & Join Trial
Open Label Pharmacokinetic Study of SAR302503 in Subjects With Hepatic Impairment PHASE1 Primary Objective:
To study the effect of mild and moderate hepatic impair...
Show More Location
Investigational Site Number 840003
Learn More & Join Trial