Claims for Patent: 11,633,489

Summary for Patent: 11,633,489

Title:	Iron carbohydrate complex for treatment of iron deficiency of a fetus or an infant
Abstract:	Disclosed herein is a pharmaceutical composition comprising an iron carbohydrate complex for use in a method for treatment or prevention of an iron deficiency of a fetus or an infant, wherein the iron carbohydrate complex is administered to the mother of the fetus or infant.
Inventor(s):	Lars Lykke THOMSEN, Tobias S. CHRISTENSEN, Hans Andreasen
Assignee:	Pharmacosmos Holding AS
Application Number:	US17/178,430
Patent Claims:	1. A method for treatment or prevention of iron deficiency of a fetus, comprising parenterally administering to the mother of the fetus during pregnancy a pharmaceutical composition comprising an effective amount of an iron carbohydrate complex comprising an iron hydrogenated oligoisomaltoside. 2. The method according to claim 1, wherein the iron deficiency is a brain iron deficiency. 3. The method according to claim 1, comprising treatment or prevention of a disorder caused by brain metal deficiency. 4. The method according to claim 1, wherein the pharmacokinetic half-life (t1/2) of the iron carbohydrate complex is 10 hours or more, 12 hours or more, 14 hours, 16 hours, 18 hours, 20 hours, or 22 hours, or more. 5. The method according to claim 1, wherein the total dose of elemental iron from the iron carbohydrate complex administered to the mother is 300 mg elemental iron or more, 400 mg elemental iron or more, 500 mg elemental iron, 600 mg elemental iron, 700 mg elemental iron, 800 mg elemental iron, 900 mg elemental iron, 1000 mg elemental iron, or more. 6. The method according to claim 1, wherein the iron carbohydrate complex comprises a carbohydrate component comprising a backbone of glucose units linked by α-1,6 glycosidic linkages and optionally branches of glucose units linked to the backbone through α-1,3 glycosidic linkages, wherein the proportion of α-1,3 glycosidic linkages to α-1,6 glycosidic linkages is less than 5:100, or is less than 1:100, or wherein the carbohydrate component does not comprise detectable branches of glucose units linked by α-1,3 glycosidic linkages to the backbone. 7. The method according to claim 1, wherein the iron carbohydrate complex is (1→6)-α-D-glucopyranan-(1→6)-D-glucitol iron(III) complex. 8. The method according to claim 1, wherein the weight average molecular weight (MW) of the carbohydrate component of the iron carbohydrate complex is 800 to 2,000 Daltons or is about 1,000 Daltons. 9. The method according to claim 1, wherein the apparent molecular weight of the iron carbohydrate complex measured relative to dextran standards, is 400,000 Daltons or less, is 300,000 Daltons or less, or is 200,000 Daltons or less. 10. The method according to claim 1, wherein the pharmaceutical composition is infused into the mother during a 3 to 30 minute time period, during a 16 to 30 minute time period, during a 5 to 25 minute time period, or during a 10 to 20 minute time period. 11. The method according to claim 1, wherein the iron carbohydrate complex is administered to the mother during the first trimester of pregnancy, during the second trimester of pregnancy, or during the third trimester of pregnancy. 12. The method according to claim 1, wherein the mother is subjected to a further administration of the iron carbohydrate complex during pregnancy or the breastfeeding period, and/or wherein a further administration of the iron carbohydrate complex is performed 1 month to 12 months after the previous administration. 13. The method according to claim 1, wherein the administration of the iron carbohydrate complex prevents or treats abnormal development of the fetal brain or wherein the administration of the iron carbohydrate complex prevents or treats abnormal development of the fetal substantia nigra, thalamus, putamen, ventral midbrain, or pallidum. 14. The method according to claim 1, wherein the iron carbohydrate complex administered to the mother supports cognitive, motor, social-emotional, or neurophysiologic development of the fetus. 15. The method according to claim 3, wherein the disorder is caused by brain iron deficiency, resulting in copper or zinc imbalance. 16. The method according to claim 3, wherein the disorder caused by brain metal deficiency is at least one of restless leg syndrome (RLS), attention deficit hyperactivity disorder (ADHD), attention deficit disorder (ADD), absence seizure, bipolar disorder, schizophrenia, obsessive-compulsive disorder (OCD), autism, borderline personality disorder (BPD), Alzheimer's disease and Parkinson's disease. 17. The method according to claim 1, wherein the maximum concentration of serum total iron (Cmax) after administering the pharmaceutical composition is between 99 μg/dl and 681 μg/dl. 18. A method for treatment or prevention of iron deficiency of an infant, comprising parenterally administering to the mother of the infant during breastfeeding an effective amount of a pharmaceutical composition comprising an iron carbohydrate complex to increase the concentration of iron in the maternal milk, wherein the iron carbohydrate complex comprises an iron hydrogenated oligoisomaltoside. 19. The method according to claim 1, wherein the iron carbohydrate complex is iron isomaltoside 1000. 20. The method according to claim 1, wherein: the iron carbohydrate complex is iron isomaltoside 1000; the pharmaceutical composition is intravenously infused into the mother for 20to 30 min; and wherein the dose of elemental iron from the iron carbohydrate complex administered to the mother is 800 mg elemental iron or more, or is 1000 mg elemental iron. 21. The method according to claim 18, wherein the iron carbohydrate complex is iron isomaltoside 1000. 22. The method according to claim 18, wherein: the iron carbohydrate complex is iron isomaltoside 1000; the pharmaceutical composition is intravenously infused into the mother for 20to 30 min; and wherein the dose of elemental iron from the iron carbohydrate complex administered to the mother is 800 mg elemental iron or more, or is 1000 mg elemental iron.