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BELEODAQ® (Belinostat)

July 24, 2014May 6, 2020 RR FDA Approvals
Non-Hodgkin Lymphoma

The FDA on July 3, 2014 granted accelerated approval to BELEODAQ® for the treatment of patients with relapsed or refractory Peripheral T-Cell Lymphoma (PTCL). BELEODAQ® is a product of Spectrum Pharmaceuticals, Inc.

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Efficacy and safety of continued zoledronic acid every 4 weeks versus every 12 weeks in women with bone metastases from breast cancer Results of the OPTIMIZE-2 trial
ZYDELIG® (Idelalisib)

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