Auris formulations for treating otic diseases and conditions
Disclosed herein are compositions and methods for the treatment of otic disorders with immunomodulating agents and auris pressure modulators. In these methods, the auris compositions and formulations are administered locally to an individual afflicted with an otic disorder, through direct application of the immunomodulating and/or auris pressure modulating compositions and formulations onto the auris media and/or auris interna target areas, or via perfusion into the auris media and/or auris interna structures.
1. A pharmaceutical composition comprising: one and no more than one growth factor selected from brain-derived neurotrophic factor (BDNF) or neurotrophin-3, or pharmaceutically acceptable salt thereof, wherein the pharmaceutical composition is a thermoreversible gel formulated for intratympanic administration, wherein the pharmaceutical composition comprises from 14% to 17% by weight of Poloxamer 407, and wherein the pharmaceutical composition provides sustained release of therapeutically effective amount of the growth factor into the ear following a single administration.
2. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition has a gelation temperature of from 20° C. to 30° C.
3. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition has a pH of from 7.0 to 8.0.
4. The pharmaceutical composition of claim 3 , wherein the pharmaceutical composition further comprises a buffering agent.
5. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition has an osmolarity of from 250 mOsm/L to 320 mOsm/L.
6. The pharmaceutical composition of claim 5 , wherein the pharmaceutical composition further comprises sodium chloride.
7. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises from 14% to 16% by weight of the poloxamer.
8. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises from 15% to 16% by weight of the poloxamer.
9. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated to provide sustained release of the growth factor into an inner ear for a period of at least 3 days following a single administration.
10. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated to provide sustained release of the growth factor into an inner ear for a period of at least 5 days following a single administration.
11. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated to provide sustained release of the growth factor into an inner ear for a period of at least 7 days following a single administration.
12. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition is formulated to provide sustained release of the growth factor into an inner ear for a period of at least 14 days following a single administration.
13. The pharmaceutical composition of claim 1 , wherein the growth factor is neurotrophin-3.
14. The pharmaceutical composition of claim 1 , wherein the growth factor is BDNF.
15. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition comprises between about 0.1 mg/ml to about 5 mg/ml of the growth factor.
16. The pharmaceutical composition of claim 1 , wherein the growth factor is dissolved in the pharmaceutical composition.
17. The pharmaceutical composition of claim 15 , wherein the pharmaceutical composition comprises between about 0.5 mg/ml to about 5 mg/ml of the growth factor.
18. The pharmaceutical composition of claim 15 , wherein the pharmaceutical composition comprises between about 0.1 mg/ml to about 0.5 mg/ml of the growth factor.
19. The pharmaceutical composition of claim 1 , wherein the composition comprises: between about 0.1 mg/ml to about 20 mg/ml of the growth factor.
20. The pharmaceutical composition of claim 1 , wherein the composition comprises: between about 0.1 mg/ml to about 10 mg/ml of the growth factor.