Individual Patient Compassionate Use of Fedratinib

Clinical Trial Description

This program is being offered on a patient by patient basis and will require company, Institutional Review Board/Independent Ethics Committee and Single Patient IND approval. ;

Study Design

See also
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Active, not recruiting	`NCT03952039` - An Efficacy and Safety Study of Fedratinib Compared to Best Available Therapy in Subjects With DIPSS-intermediate or High-risk Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, or Post-essential Thrombocythemia Myelofibrosis and Previously Treated With Ruxolitinib	Phase 3
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NCT number	NCT03723148
Study type	Expanded Access
Source	Celgene
Contact	Celgene Medical Information
Phone	1-888-771-0141
Email	medinfo@celgene.com
Status	Available
Phase

Individual Patient Compassionate Use of Fedratinib

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms