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OXBRYTA® (Voxelotor)

November 29, 2019April 5, 2020 RR FDA Approvals
Anemia - Sickle Cell

The FDA on November 25, 2019 granted accelerated approval to OXBRYTA® for adults and pediatric patients 12 years of age and older with Sickle Cell disease. OXBRYTA® is a product of Global Blood Therapeutics.

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First Line Combination of TECENTRIQ® and AVASTIN® Improves Survival in Hepatocellular Carcinoma
CALQUENCE® (Acalabrutinib)

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