US2018042959A1PendingUtilityA1
Glucocerebroside treatment of disease
Est. expiryFeb 27, 2023(expired)· nominal 20-yr term from priority
A61P 37/02A61P 9/00A61P 3/10A61P 9/10A61P 5/00A61P 37/04A61P 7/00A61P 31/20A61P 35/00A61P 25/28A61P 31/18A61P 31/12A61P 31/04A61P 3/00A61P 31/14A61P 31/00A61P 29/00A61P 27/02A61K 31/7028A61P 11/00A61K 31/00A61K 31/7032A61K 38/1709A61K 31/70A61K 31/739A61P 1/04A61K 31/7004A61P 1/00A61K 38/00A61P 19/00A61P 17/00A61P 1/16A61K 35/17A61K 35/15
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Claims
Abstract
The present invention provides a method for the treatment of immune mediated or immune related diseases or disorders, infectious diseases, metabolic disorders and cancer in mammalian subjects. This method comprises the administration of a naturally occurring, mammalian intermediary metabolite or T cell receptor ligand, preferably a glucosylceramide, to a mammalian subject. In a preferred embodiment, such mammalian subjects are human beings.
Claims
exact text as granted — not AI-modified1 - 112 . (canceled)
113 . The method of claim 114 , wherein said administering step comprises oral, intravenous, intraperitoneal, parenteral, mucosal, rectal or subcutaneous administration, or any combination thereof.
114 . A method for treating Inflammatory Bowel Disease (IBD) in a mammalian subject, comprising:
administering to a mammalian subject having Inflammatory Bowel Disease a pharmaceutical composition comprising a therapeutically effective amount of a β-glucosylceramide, wherein said administration improves the Inflammatory Bowel Disease in said mammalian subject.
115 . The method of claim 114 , wherein the β-glucosylceramide is soy-derived.
116 . The method according to claim 114 , wherein said subject is subjected to fasting for a minimum of twelve hours prior to said administration of said β-glucosylceramide.
117 . The method of claim 116 , wherein the β-glucosylceramide is soy-derived.
118 . The method of claim 114 , wherein the mammalian subject is a human subject.
119 . The method of claim 118 , wherein said administering step comprises enteral administration of said β-glucosylceramide.
120 . The method of claim 118 , wherein said administering step comprises parenteral administration of said β-glucosylceramide.
121 . The method of claim 115 , wherein the mammalian subject is a human subject.
122 . The method of claim 121 , wherein said administering step comprises enteral administration of said β-glucosylceramide.
123 . The method of claim 121 , wherein said administering step comprises parenteral administration of said β-glucosylceramide.
124 . The method of claim 116 , wherein the mammalian subject is a human subject.
125 . The method of claim 124 , wherein said administering step comprises enteral administration of said β-glucosylceramide.
126 . The method of claim 124 , wherein said administering step comprises parenteral administration of said β-glucosylceramide.
127 . The method of claim 117 , wherein the mammalian subject is a human subject.
128 . The method of claim 127 , wherein said administering step comprises enteral administration of said β-glucosylceramide.
129 . The method of claim 127 , wherein said administering step comprises parenteral administration of said β-glucosylceramide.
130 . The method of claim 118 , wherein the Inflammatory Bowel Disease is ulcerative Colitis.
131 . The method of claim 130 , wherein said administering step comprises rectal administration.
132 . The method of claim 130 , wherein said administering step comprises parenteral administration.
133 . The method of claim 130 , wherein said administering step comprises enteral administration.
135 . The method of claim 118 , wherein said Inflammatory Bowel Disease is Crohn's disease.
136 . The method of claim 135 , wherein said administering step comprises parenteral administration.
137 . The method of claim 135 , wherein said administering step comprises enteral administration.Cited by (0)
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