Antisense modulation of PTP1B expression
View Patent ↗Provided herein are methods, compounds, and compositions for reducing expression of PTP1B mRNA and protein in an animal. Such methods, compounds, and compositions are useful to treat, prevent, delay, or ameliorate metabolic disease, for example, diabetes, or a symptom thereof.
1. A pharmaceutical composition suitable for parenteral administration to an animal comprising an aqueous solution, said aqueous solution comprising:
a pharmaceutically acceptable carrier or diluent; and
a single stranded modified oligonucleotide targeted to PTP1B consisting of 20 linked nucleosides having a nucleobase sequence consisting of SEQ ID NO: 26, or salt thereof,
wherein the carrier or diluent is sterile and the aqueous solution is suitably viscous for parenteral administration.
2. The pharmaceutical composition of claim 1 , wherein the aqueous solution suitably viscous for parenteral administration has a viscosity level less than 40 centipoise (cP).
3. The pharmaceutical composition of claim 2 , wherein the parenteral administration is subcutaneous injection.
4. The pharmaceutical composition of claim 2 , wherein the parenteral administration is intravenous infusion.
5. The pharmaceutical composition of claim 1 , wherein the modified oligonucleotide comprises:
a gap segment consisting of ten linked deoxynucleosides;
a 5′ wing segment consisting of five linked nucleosides; and
a 3′ wing segment consisting of five linked nucleosides;
wherein the gap segment is positioned between the 5′ wing segment and the 3′ wing segment, wherein each nucleoside of each wing segment comprises a 2′-O-methoxyethyl sugar, wherein each internucleoside linkage is a phosphorothioate linkage, and wherein each cytosine of the modified oligonucleotide is a 5-methylcytosine.
6. The pharmaceutical composition of claim 5 , wherein the aqueous solution suitably viscous for parenteral administration has a viscosity level less than 40 centipoise (cP).
7. The pharmaceutical composition of claim 6 , wherein the aqueous solution comprises the modified oligonucleotide targeted to PTP1B at a concentration of about 165-185 mg/mL.
8. The pharmaceutical composition of claim 7 , wherein the aqueous solution has a temperature of about 25° C.
9. The pharmaceutical composition of claim 8 , wherein the parenteral administration is subcutaneous injection.
10. The pharmaceutical composition of claim 8 , wherein the parenteral administration is intravenous infusion.
11. The pharmaceutical composition of claim 1 , wherein the pharmaceutically acceptable carrier or diluent is water.
12. The pharmaceutical composition of claim 11 , wherein the modified oligonucleotide comprises:
a gap segment consisting of ten linked deoxynucleosides;
a 5′ wing segment consisting of five linked nucleosides; and
a 3′ wing segment consisting of five linked nucleosides;
wherein the gap segment is positioned between the 5′ wing segment and the 3′ wing segment, wherein each nucleoside of each wing segment comprises a 2′-O-methoxyethyl sugar, wherein each internucleoside linkage is a phosphorothioate linkage, and wherein each cytosine of the modified oligonucleotide is a 5-methylcytosine.
13. The pharmaceutical composition of claim 12 , wherein the aqueous solution suitably viscous for parenteral administration has a viscosity level less than 40 centipoise (cP).
14. The pharmaceutical composition of claim 13 , wherein the aqueous solution comprises the modified oligonucleotide targeted to PTP1B at a concentration of about 165-185 mg/mL.
15. The pharmaceutical composition of claim 14 , wherein the aqueous solution has a temperature of about 25° C.
16. The pharmaceutical composition of claim 15 , wherein the parenteral administration is subcutaneous injection.
17. The pharmaceutical composition of claim 16 , wherein the parenteral administration is intravenous infusion.