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Sanofi: EC Oks Enjaymo For Treatment Of Hemolytic Anemia In Adult With Cold Agglutinin Disease

PARIS (dpa-AFX) - Sanofi - Aventis Groupe said that the European Commission has granted marketing authorization for Enjaymo (sutimlimab) for the treatment of hemolytic anemia in adult patients ....

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Global Blood Therapeutics, Inc.: MHRA Grants Marketing Authorization for GBT's Oxbryta (voxelotor) for Use in Great Britain for the Treatment of Hemolytic Anemia in Patients with Sickle Cell Disease Age 12 Years and Older

Voxelotor is the first medicine approved in Great Britain to directly inhibit sickle hemoglobin (HbS) polymerization, the underlying molecular cause of sickle cell diseaseSOUTH SAN FRANCISCO, Calif., July ....

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DelveInsight Business Research, LLP: Warm Autoimmune Hemolytic Anemia Market is Expected to Witness Growth at an Accelerated CAGR of 14.7% in the 7MM for the Study Period 2018-30, Assesses DelveInsight

LAS VEGAS, Feb. 28, 2022 /PRNewswire/ The launch of key Warm Autoimmune Hemolytic Anemia (WAIHA) assets such as Fostamitinib (Rigel Pharmaceuticals) and APL2 (Apellis Pharmaceuticals), which ....

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Global Blood Therapeutics, Inc.: European Commission Approves Oxbryta (voxelotor) for the Treatment of Hemolytic Anemia in Patients with Sickle Cell Disease Age 12 Years and Older

The first sickle hemoglobin polymerization inhibitor approved in Europe, Oxbryta increases hemoglobin levels and reduces sickling and hemolysis - the cause of long-term complications of sickle cell diseaseSOUTH ....

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Global Blood Therapeutics, Inc.: Positive Early Access to Medicines Scheme (EAMS) Scientific Opinion Awarded to GBT's Voxelotor for the Treatment of Haemolytic Anaemia Due to Sickle Cell Disease

LONDON, Jan. 27, 2022 (GLOBE NEWSWIRE) Global Blood Therapeutics (GBT) today announced that the UK's Medicines and Healthcare products Regulatory Agency (MHRA) has awarded a positive scientific opinion ....

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