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Friday, January 05, 2018 -- Novartis’ drug Promacta (eltrombopag) has secured breakthrough therapy designation from the US Food and Drug Administration (FDA) for first-line treatment of severe aplastic anemia (SAA).

Friday, January 05, 2018 -- Eltrombopag (Promacta) has been granted a breakthrough therapy designation by the FDA for use in combination with standard immunosuppressive therapy for the first-line treatment of patients with severe aplastic anemia.

Friday, January 05, 2018 -- The safety profile of CERA is similar for children as for adults.

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