BIO-ERODIBLE OCULAR IMPLANTS FOR TREATMENT OF CONDITIONS OF THE EYE
The present disclosure relates to intraocular, drug-eluting microparticle implants, as well as a dry microparticle formulation comprising a plurality of drug-eluting microparticle implants, for treating a condition of the eye, wherein the implant is configured to deliver a drug to the eye without a carrier. The present disclosure also relates to methods of treating a condition of the eye by delivering one or more drugs from drug-eluting implants or a dry microparticle formulation to the anterior chamber, posterior chamber (e.g., sulcus), iridocorneal angle, sclera, cornea, limbus, subconjunctival space, sub-Tenon's space, and vitreous.
1 . A method for treating a condition of an eye of a subject, the method comprising:
implanting a dry implant formulation in the eye of the subject without a carrier, the dry implant formulation comprising a plurality of drug-eluting microparticle implants,
wherein at least one drug is delivered from the plurality of drug-eluting microparticle implants to the eye to reduce a symptom associated with the condition of the eye.
2 . The method of claim 1 , wherein each of the plurality of drug-eluting microparticle implants comprises a drug-eluting matrix.
3 . The method of claim 2 , wherein the drug-eluting matrix comprises a bio-erodible polymer and the at least one drug.
4 . The method of claim 3 , wherein the bio-erodible polymer comprises poly(lactic-co-glycolic acid) (PLGA), poly(lactic acid) (PLA), poly-epsilon-caprolactone (PCA), or poly(glycolic acid) (PGA).
5 . (canceled)
6 . The method of claim 1 , wherein each of the plurality of the drug-eluting microparticle implants has a diameter of between about 1 μm and about 500 μm.
7 . (canceled)
8 . The method of claim 1 , wherein the condition of the eye is glaucoma and/or dry eye disease.
9 . The method of claim 1 , wherein the dry implant formulation is implanted in one or more of a sulcus, a posterior chamber, an anterior chamber, a vitreous, a sub-Tenon's space, and a subconjunctival space of the eye.
10 . The method of claim 1 , wherein the at least one drug comprises a prostamide analog or a prostaglandin analog.
11 . The method of claim 1 , wherein the at least one drug comprises a beta-adrenergic blocker, a carbonic anhydrase inhibitor, a rho-kinase inhibitor, a nerve growth factor, an anti-VEGF antibody, sirolimus, tacrolimus, everolimus, or cyclosporine.
12 - 13 . (canceled)
14 . The method of claim 1 , wherein the plurality of the microparticle implants in total is configured to deliver the at least one drug to the eye at a rate of between about 1 ng/day and about 50 μg/day.
15 . The method of claim 1 , wherein the plurality of the microparticle implants in total is configured to deliver the at least one drug to the eye at a rate of between about 5 ng/day and about 2000 ng/day.
16 . The method of claim 1 , wherein the dry implant formulation is configured to deliver the at least one drug to the eye over a period of time, wherein the period of time is at least 1 month, at least 4 months, at least 6 months, at least 8 months, at least 1 year, at least 2 years, or at least 3 years.
17 . The method of claim 1 , wherein at least a subset of the plurality of the microparticle implants comprises an imaging agent.
18 - 20 . (canceled)
21 . The method of claim 1 , wherein the plurality of drug-eluting microparticle implants comprises a first microparticle implant comprising a first drug of the at least one drug and a second microparticle implant comprising a second, different drug of the at least one drug.
22 . The method of claim 21 , wherein the first drug is a beta-adrenergic blocker.
23 . The method of claim 22 , wherein the beta-adrenergic blocker is a timolol.
24 . (canceled)
25 . The method of claim 22 , wherein the second drug is a carbonic anhydrase inhibitor.
26 . The method of claim 25 , wherein the carbonic anhydrase inhibitor is a dorzolamide or a brinzolamide.
27 . (canceled)
28 . The method of claim 22 , wherein the second drug is a prostaglandin analog or a prostamide analog.
29 . The method of claim 28 , wherein the prostaglandin analog is latanoprost, travoprost, tafluprost, or unoprostone, and the prostamide analog is bimatoprost.
30 . (canceled)
31 . The method of claim 22 , wherein the second drug is a rho-kinase inhibitor. 32 - 37 . (canceled)
38 . The method of claim 21 , wherein the condition is glaucoma, the first drug is a timolol, and the second drug is a dorzolamide or a brinzolamide, and wherein the dry implant formulation is implanted in sub-Tenon's space.
39 . The method of claim 1 , wherein each of the plurality of drug-eluting microparticle implants is a microsphere.
40 . The method of claim 1 , wherein each of the plurality of drug-eluting microparticle implants comprises a bio-erodible polymer, and at least a majority of the plurality of drug-eluting microspheres have been heated above the glass transition temperature of the bio-erodible polymer.
41 . The method of claim 1 , further comprising a binding agent.
42 . The method dry implant formulation of claim 41 , wherein the binding agent is selected from the group consisting of: a sugar, a gelatin, a collagen, polyethylene glycol (PEG), a starch, a cellulose, an alginate, and a chitosan.
43 . (canceled)
44 . The method of claim 1 , wherein the dry implant formulation is malleable, and does not readily dissociate into individual implants.
45 - 114 . (canceled)
115 . The method of claim 1 , wherein the dry implant formulation is a first dry implant formulation and the method further comprises implanting a second dry implant formulation, the second dry implant formulation comprising a second plurality of drug-eluting microparticle implants.
116 . The method of claim 115 , wherein the first dry implant formulation and the second dry implant formulation are implanted sequentially.
117 . The method of claim 115 , wherein the second dry implant formulation is implanted in a different location in the eye than the first dry implant formulation.
118 . The method of claim 8 , wherein the condition of the eye is glaucoma, and the symptom associated with glaucoma is increased ocular pressure.