US 12,202,900 B2
Compositions and methods for treating immune thrombocytopenia
Hans De Haard, Oudelande (NL); Peter Ulrichts, Destelbergen (BE); Thierry Cousin, Bordeaux (FR); Nicolas Leupin, Zurich (CH); Torsten Dreier, Sint Martens Latem (BE); and Tonke Van Bragt, Boxtel (NL)
Assigned to argenx BV, Ghent (BE)
Filed by argenx BV, Ghent (BE)
Filed on Jun. 7, 2019, as Appl. No. 16/435,166.
Claims priority of provisional application 62/732,414, filed on Sep. 17, 2018.
Claims priority of provisional application 62/731,947, filed on Sep. 16, 2018.
Claims priority of provisional application 62/682,805, filed on Jun. 8, 2018.
Prior Publication US 2020/0024344 A1, Jan. 23, 2020
Int. Cl. C07K 16/28 (2006.01); C07K 14/47 (2006.01); A61K 45/06 (2006.01)
CPC C07K 16/283 (2013.01) [C07K 14/4703 (2013.01); A61K 45/06 (2013.01); C07K 2317/41 (2013.01); C07K 2317/52 (2013.01)] 14 Claims
 
1. A method of treating a human subject that has newly diagnosed, persistent, or chronic immune thrombocytopenia (ITP), the method comprising administering to the subject a human neonatal Fc receptor (hFcRn) antagonist, wherein the hFcRn antagonist is administered intravenously once weekly at a dose of about 5 mg/kg to about 10 mg/kg at least four times, wherein the hFcRn antagonist consists of a variant Fc region consisting of two Fc domains which form a homodimer, wherein the amino acid sequence of each of the Fc domains consists of SEQ ID NO: 1, SEQ ID NO: 2, or SEQ ID NO: 3, wherein the human subject has a platelet count of ≤30×109/L on standard-of-care treatment with at least one compound approved for standard-of-care treatment for ITP prior to administering the hFcRn antagonist, and wherein the subject achieves a platelet count of >50×109/L after administering four doses of the hFcRn antagonist, thereby treating the subject.