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INREBIC® (Fedratinib)

August 17, 2019April 5, 2020 RR FDA Approvals
Myelofibrosis

The FDA on August 16, 2019 approved INREBICĀ® for adults with intermediate-2 or high-risk Primary or Secondary (post-Polycythemia Vera or post-Essential Thrombocythemia) Myelofibrosis (MF). INREBICĀ® is a product of Impact Biomedicines, Inc.

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  • FDA Approves INREBICĀ® for Myelofibrosis

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ROZLYTREK® (Entrectinib)
Periprocedural Bridging Increases Bleeding Risk without Reduction in VTE Rates for Patients on Long Term Anticoagulants

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