GHRH or analogues thereof for use in treatment of hepatic disease
The present application relates to novel methods for preventing, slowing the progression of, or treating nonalcoholic fatty liver (NAFL), nonalcoholic steatohepatitis (NASH), and/or liver fibrosis, and/or reducing the risks of liver cancer in subjects, such as HIV-infected subjects, using a GHRH molecule, e.g., trans-3-hexenoyl-GHRH (1-44) -NH 2 , or a pharmaceutically acceptable salt thereof. The subjects may have particular pathological features such as liver fibrosis, a hepatic fat fraction (HFF) of at least about 10%, serum alanine aminotransferase (ALT) levels of at least about 30 U/L, and/or a NAFLD Activity Score (NAS) of at least 4 or 5.
1. A method for treating nonalcoholic fatty liver (NAFL) or nonalcoholic steatohepatitis (NASH) in a subject in need thereof comprising administering an effective amount of trans-3-hexenoyl-GHRH (1-44) -NH 2 or a pharmaceutically acceptable salt thereof to said subject, wherein said subject has at least one of:
(i) a hepatic fat fraction (HFF) of at least about 15% as measured by proton magnetic resonance spectroscopy ( 1 H MRS);
(ii) serum alanine aminotransferase (ALT) levels of at least about 35 U/L;
(iii) a NAFLD Activity Score (NAS) of at least 6 as measured by the NAS Clinical Research Network (NAS CRN) scoring system;
(iv) a reduction of HFF by at least 4% (absolute reduction) following the treatment; and
(v) liver fibrosis.
2. The method of claim 1 , wherein said subject has an HFF of at least about 20%.
3. The method of claim 1 , wherein the HFF is reduced by at least 4% (absolute reduction) in said subject.
4. The method of claim 1 , wherein said subject has serum ALT levels of at least about 35 U/L.
5. The method of claim 1 , wherein said subject has a NAS of at least 6.
6. The method of claim 1 , wherein said subject has liver fibrosis.
7. The method of claim 1 , wherein said subject suffers from human immunodeficiency virus (HIV) infection.
8. The method claim 1 , wherein said subject has a body mass index (BMI) of at least about 25.
9. The method of claim 1 , wherein said pharmaceutically acceptable salt of trans-3-hexenoyl-GHRH (1-44) -NH 2 is an acetate salt.
10. The method of claim 1 , wherein said trans-3-hexenoyl-GHRH (1-44) -NH 2 or pharmaceutically acceptable salt thereof is administered by subcutaneous injection.
11. The method of claim 1 , wherein said trans-3-hexenoyl-GHRH (1-44) -NH 2 or pharmaceutically acceptable salt thereof is present in a pharmaceutical composition comprising at least one pharmaceutically acceptable excipient.
12. The method of claim 11 , wherein said trans-3-hexenoyl-GHRH (1-44) -NH 2 or pharmaceutically acceptable salt thereof is present in said pharmaceutical composition at a dose of about 1 mg/ml to about 10 mg/ml.
13. A method for (i) reducing the progression of liver fibrosis or (ii) reducing liver fibrosis in a subject, comprising administering an effective amount of trans-3-hexenoyl-GHRH (1-44) -NH 2 or a pharmaceutically acceptable salt thereof to said subject, wherein said subject has at least one of:
(i) a fibrosis score of at least 1C, prior to the treatment;
(ii) an HFF of at least about 10%;
(iii) serum ALT levels of at least about 30 U/L; and
(iv) a NAFLD Activity Score (NAS) of at least 2 as measured by the NAS Clinical Research Network (NAS CRN) scoring system.
14. The method of claim 13 , wherein said subject has a fibrosis score of at least 1C prior to the treatment.
15. The method of claim 13 , wherein said subject has a fibrosis score of at least 2 prior to the treatment.
16. The method of claim 13 , wherein said subject has an HFF of at least about 15%.
17. The method of claim 13 , wherein said subject has an HFF of at least about 20%.
18. The method of claim 13 , wherein said subject has serum ALT levels of at least about 30 U/L.
19. The method of claim 13 , wherein said subject has a NAFLD Activity Score (NAS) of at least 2 as measured by the NAS Clinical Research Network (NAS CRN) scoring system.
20. The method of claim 13 , wherein said subject suffers from human immunodeficiency virus (HIV) infection.
21. The method of claim 13 , wherein said subject has a body mass index (BMI) of at least about 25.
22. The method of claim 13 , wherein said pharmaceutically acceptable salt of trans-3-hexenoyl-GHRH (1-44) -NH 2 is an acetate salt.
23. The method of claim 13 , wherein said trans-3-hexenoyl-GHRH (1-44) -NH 2 or pharmaceutically acceptable salt thereof is administered by subcutaneous injection.
24. The method of claim 13 , wherein said trans-3-hexenoyl-GHRH (1-44) -NH 2 or pharmaceutically acceptable salt thereof is present in a pharmaceutical composition comprising at least one pharmaceutically acceptable excipient.
25. The method of claim 24 , wherein said trans-3-hexenoyl-GHRH (1-44) -NH 2 or pharmaceutically acceptable salt thereof is present in said pharmaceutical composition at a dose of about 1 mg/ml to about 10 mg/ml.
26. A method for reducing the risk of developing liver cancer in a subject suffering from nonalcoholic fatty liver (NAFL) or nonalcoholic steatohepatitis (NASH) comprising administering an effective amount of trans-3-hexenoyl-GHRH (1-44) -NH 2 or a pharmaceutically acceptable salt thereof to said subject, wherein said subject has at least one of:
(i) a hepatic fat fraction (HFF) of at least about 15% as measured by proton magnetic resonance spectroscopy ( 1 H MRS);
(ii) serum alanine aminotransferase (ALT) levels of at least about 35 U/L;
(iii) a NAFLD Activity Score (NAS) of at least 6 as measured by the NAS Clinical Research Network (NAS CRN) scoring system;
(iv) a reduction of HFF by at least 4% (absolute reduction) following the treatment; and
(v) liver fibrosis.
27. The method of claim 26 , wherein said pharmaceutically acceptable salt of trans-3-hexenoyl-GHRH (1-44) -NH 2 is an acetate salt.
28. The method of claim 26 , wherein said trans-3-hexenoyl-GHRH (1-44) -NH 2 or pharmaceutically acceptable salt thereof is administered by subcutaneous injection.
29. The method of claim 26 , wherein said trans-3-hexenoyl-GHRH (1-44) -NH 2 or pharmaceutically acceptable salt thereof is present in a pharmaceutical composition comprising at least one pharmaceutically acceptable excipient.
30. The method of claim 29 , wherein said trans-3-hexenoyl-GHRH (1-44) -NH 2 or pharmaceutically acceptable salt thereof is present in said pharmaceutical composition at a dose of about 1 mg/ml to about 10 mg/ml.