Amgen has announced that The Lancet published results from a Phase III randomized, double-blind, placebo-controlled study of Nplate (romiplostim) in...
Amgen announced that the FDA has approved the supplemental Biologics License Application (sBLA) for Nplate (romiplostim) for the treatment of...
Amgen announced that the FDA has approved Amgen's Supplemental Biologics License Application (sBLA) for Nplate (romiplostim) to include new data...
Amgen announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has adopted...
Novartis announced that the FDA has approved an expanded use for Promacta (eltrombopag) to include children 1 year of age...
Amgen announced the submission of a Supplemental Biologics License Application (sBLA) to the FDA for Nplate (romiplostim) to include the...
Sobi announced positive results from the AVA-PED-301 study (NCT04516967), evaluating the efficacy and safety of avatrombopag (Doptelet) for the treatment of paediatric patients with immune thrombocytopenia (ITP) of at least 6 months’ duration.
Novartis announced that the FDA has approved Promacta (eltrombopag) for the treatment of children six years and older with chronic...
Swedish Orphan Biovitrum AB (publ) (Sobi™) announced that the first patient has been dosed with Doptelet (avatrombopag), a thrombopoietin receptor agonist (TPO-RA), for treatment of immune thrombocytopenia (ITP) in pediatric patients.
Health Canada approved avatrombopag (doptelet, Sobi) to treat thrombocytopenia in adult patients with chronic immune thrombocytopenia (ITP) and in adult patients with chronic liver disease (CLD) who are scheduled to undergo an invasive procedure