Dose escalation enzyme replacement therapy for treating acid sphingomyelinase deficiency
The invention relates to dose escalation enzyme replacement therapy using acid sphingomyelinase (ASM) for the treatment of human subjects having acid sphingomyelinase deficiency (ASMD), and, in particular, patients with non-neurological manifestations of Niemann-Pick Disease (NPD), and in certain embodiments, NPD type B.
1. A method for reducing sphingomyelin accumulation in one or more organs of a human subject having an acid sphingomyelinase deficiency (ASMD), comprising:
(a) administering at least one initial dose of recombinant human acid sphingomyelinase (rhASM) to the human subject, wherein the initial dose is from 0.025 mg/kg to 0.275 mg/kg; and
(b) subsequent to the administration of the at least one initial dose, administering a higher dose of rhASM to the human subject, wherein the higher dose is from 0.1 mg/kg to 3.0 mg/kg higher than the initial dose.
2. A method for reducing sphingomyelin accumulation in one or more organs of a human subject having an acid sphingomyelinase deficiency (ASMD), comprising:
(a) administering at least one initial dose of recombinant human acid sphingomyelinase (rhASM) to the human subject, wherein the initial dose is from 0.025 mg/kg to 0.275 mg/kg; and
(b) subsequent to the administration of the at least one initial dose, administering a higher dose of rhASM to the human subject, wherein the higher dose is from 0.5 mg/kg to 2 mg/kg higher than the initial dose.
3. The method of claim 1 , wherein each dose is administered one, two, three, or four weeks after the previous dose.
4. The method of claim 2 , wherein each dose is administered one, two, three, or four weeks after the previous dose.
5. The method of claim 1 , wherein the doses are administered intravenously, intradermally, subcutaneously, or intramuscularly.
6. The method of claim 2 , wherein the doses are administered intravenously, intradermally, subcutaneously, or intramuscularly.
7. The method of claim 1 , wherein the ASMD is Niemann Pick Disease (NPD) type A or NPD type B.
8. The method of claim 2 , wherein the ASMD is Niemann Pick Disease (NPD) type A or NPD type B.
9. The method of claim 1 , wherein the human subject has a mutation in the gene encoding acid sphingomyelinase.
10. The method of claim 2 , wherein the human subject has a mutation in the gene encoding acid sphingomyelinase.
11. The method of claim 1 , wherein the one or more organs in which sphingomyelin is reduced is the liver, spleen, lungs, heart, kidney, skin, and/or brain of the human subject.
12. The method of claim 2 , wherein the one or more organs in which sphingomyelin is reduced is the liver, spleen, lungs, heart, kidney, skin, and/or brain of the human subject.
13. The method of claim 11 , wherein the one or more organs is the liver.
14. The method of claim 12 , wherein the one or more organs is the liver.
15. The method of claim 13 , wherein reduction of sphingomyelin in the liver is determined by biopsy or by a liver function test.
16. The method of claim 14 , wherein reduction of sphingomyelin in the liver is determined by biopsy or by a liver function test.
17. The method of claim 15 , wherein the liver function test assesses the concentration of alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (AP), gamma-glutamyl transferase (GGT) and/or total and direct bilirubin.
18. The method of claim 16 , wherein the liver function test assesses the concentration of alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (AP), gamma-glutamyl transferase (GGT) and/or total and direct bilirubin.