Long-acting polypeptides and methods of producing and administering same
CTP-modified human growth hormone polypeptides and pharmaceutical formulations and pharmaceutical compositions comprising the same and methods of producing, and using the same are disclosed.
1. A method for maintaining insulin-like growth factor (IGF-1) levels in a growth hormone deficient human prepubertal pediatric subject within a normal therapeutic range, comprising
administering to the growth hormone deficient human prepubertal pediatric subject a therapeutically effective amount of a glycosylated polypeptide comprising an amino terminal chorionic gonadotropin carboxy terminal peptide (CTP) of SEQ ID NO:18, a human growth hormone polypeptide, and two carboxy terminal chorionic gonadotropin CTPs, each of SEQ ID NO:18 and arranged in tandem (CTP-modified hGH polypeptide), the CTP-modified hGH polypeptide having the amino acid sequence as set forth in amino acids 27 to 301 of SEQ ID NO: 39,
wherein the therapeutically effective amount comprises a once a week dose of 0.66 milligrams per kilogram per week_(mg/kg/week), and
wherein the normal therapeutic range of IGF-1 levels is ±2 standard deviations (SDS) of the average IGF-1 levels in non-growth hormone deficient human prepubertal pediatric subjects.
2. The method of claim 1 , wherein the IGF-1 levels comprise IGF-1 levels of samples tested four days post-administration of the CTP-modified hGH polypeptide.
3. The method of claim 1 , wherein the IGF-1 levels are maintained within the normal therapeutic range of IGF-1 levels of ±2 SDS for at least 6 months.
4. The method of claim 1 , wherein the normal therapeutic range of IGF-1 levels is ±1.5 SDS of the average IGF-1 levels in non-growth hormone deficient human prepubertal pediatric subject.
5. The method of claim 1 , wherein the growth hormone deficient human prepubertal pediatric subject has a six month annualized height velocity increase of at least 12.25 centimeters (cm).
6. The method of claim 5 , wherein the six month annualized height velocity increase is at least 13.48 cm.
7. The method of claim 6 , wherein the six month annualized height velocity increase is at least 14.37 cm.
8. The method of claim 1 , wherein the normal therapeutic range of IGF-1 levels is maintained in the growth hormone deficient human prepubertal pediatric subject for between about two weeks to four months.
9. The method of claim 1 , wherein the normal therapeutic range of IGF-1 levels is maintained in the growth hormone deficient human prepubertal pediatric subject for four months.
10. The method of claim 1 , wherein the normal therapeutic range of IGF-1 levels is maintained in the growth hormone deficient human prepubertal pediatric subject for six months.
11. The method of claim 1 , wherein the growth hormone deficient human prepubertal pediatric subject is a naïve growth hormone deficient human prepubertal pediatric subject.
12. The method of claim 1 , wherein a mean time interval of IGF-1 levels that are within the normal therapeutic range after the last dose administration is
(i) at least 119±66.51 hrs;
(ii) at least 120±66.24 hrs; or
(iii) at least 146±50.62 hrs.
13. The method of claim 1 , wherein the CTP-modified hGH polypeptide is encoded by the nucleic acid sequence set forth in nucleotides 89 to 913 of SEQ ID NO: 45.