Triglyceride otic formulations and uses thereof
Disclosed herein are triglyceride based formulations, compositions, and methods for the treatment of otic diseases and conditions. Such triglyceride based formulations and compositions are derived from medium chain triglycerides and allow for the delivery of a variety of therapeutic agents to the outer, middle, and/or inner ear.
1. An otic pharmaceutical formulation comprising:
a) a therapeutic agent, or pharmaceutically acceptable prodrug or salt thereof; and
b) triglycerides comprising medium chain fatty acids;
wherein:
(i) the otic pharmaceutical formulation comprises at least about 50% by weight of the triglycerides
(ii) the therapeutic agent is an NMDA receptor antagonist
(iii) the otic pharmaceutical formulation is essentially free of antibiotics; and
(iv) the otic pharmaceutical formulation provides sustained release of the therapeutic agent for a period of at least 3 days.
2. The otic pharmaceutical formulation of claim 1 , wherein the triglycerides are present in an amount that is sufficient to provide sustained release of the therapeutic agent.
3. The otic pharmaceutical formulation of claim 1 , wherein the formulation is capable of being injected via an 18-30 gauge needle.
4. The otic pharmaceutical formulation of claim 1 , wherein the triglycerides are derived from glycerol and medium chain fatty acids.
5. The otic pharmaceutical formulation of claim 4 , wherein the medium chain fatty acids are caproic acid (hexanoic acid), enanthic acid (heptanoic acid), caprylic acid (octanoic acid), pelargonic acid (nonanoic acid), capric acid (decanoic acid), undecylenic acid (undec-10-enoic acid), lauric acid (dodecanoic acid), or a combination thereof.
6. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation comprises between about 50% to about 99.99% by weight of the triglycerides.
7. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation further comprises at least one viscosity modulating agent.
8. The otic pharmaceutical formulation of claim 7 , wherein the at least one viscosity modulating agent is silicon dioxide, povidone, carbomer, poloxamer, or a combination thereof.
9. The otic pharmaceutical formulation of claim 8 , wherein the viscosity modulating agent is silicon dioxide.
10. The otic pharmaceutical formulation of claim 1 , wherein the therapeutic agent, or pharmaceutically acceptable prodrug or salt thereof is gacyclidine free base.
11. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation comprises between about 60% to about 99.99% by weight of the triglycerides.
12. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation comprises between about 70% to about 99.99% by weight of the triglycerides.
13. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation comprises between about 80% to about 99.99% by weight of the triglycerides.
14. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation comprises between about 85% to about 99.99% by weight of the triglycerides.
15. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation comprises between about 90% to about 99.99% by weight of the triglycerides.
16. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation comprises between about 95% to about 99.99% by weight of the triglycerides.
17. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation has a viscosity between about 10 cP to about 10,000 cP.
18. The otic pharmaceutical formulation of claim 1 , wherein the therapeutic agent is gacyclidine.
19. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation comprises between about 0.01% to about 20% by weight of the therapeutic agent, or pharmaceutically acceptable prodrug or salt thereof.
20. The otic pharmaceutical formulation of claim 1 , wherein the retention time of the formulation in the inner ear is at least 1 day.
21. The otic pharmaceutical formulation of claim 1 , wherein the retention time of the formulation in the inner ear is at least 3 days.
22. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation is free or substantially free of water, C1-C6 alcohols or C1-C6 glycols, C1-C4 alcohols or C1-C4 glycols, or any combination thereof.
23. The otic pharmaceutical formulation of claim 1 , further comprising a drug delivery device selected from a needle and syringe, a pump, a microinjection device, a wick, a spongy material and combinations thereof.
24. The otic pharmaceutical formulation of claim 1 for use in the treatment of an otic disease or condition associated with the inner ear.
25. The otic pharmaceutical formulation of claim 1 , wherein the otic disease or condition is ceruminosis or ceruminosis associated with an otic disease or condition, ear pruritus, otitis externa, otalgia, tinnitus, vertigo, ear fullness, hearing loss, Meniere's disease, sensorineural hearing loss, noise induced hearing loss, age related hearing loss (presbycusis), auto immune ear disease, ototoxicity, excitotoxicity, endolymphatic hydrops, labyrinthitis, Ramsay Hunt's Syndrome, vestibular neuronitis, or microvascular compression syndrome, hyperacusis, presbystasis, central auditory processing disorder, auditory neuropathy, improvement of cochlea implant performance, or a combination thereof.
26. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation consists essentially of the therapeutic agent and the triglycerides.
27. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation is formulated for intratympanic administration.
28. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation has pH range of about 7.0 to 8.0.
29. The otic pharmaceutical formulation of claim 1 , wherein the otic pharmaceutical formulation is essentially free of antimicrobial agents.
30. A method of treating an otic disease or condition in a subject in need thereof, the method comprising administering to the subject the otic pharmaceutical formulation of claim 1 .