Claims for Patent: 7,959,942

Summary for Patent: 7,959,942

Title:	Bioabsorbable medical device with coating
Abstract:	A biodegradable, bioabsorbable medical device with a coating for capturing progenitor endothelial cells in vivo and delivering a therapeutic agent at the site of implantation. The coating on the medical device is provided with a biabsorbable polymer composition such as a bioabsorbable polymer, copolymer, or terpolymer, and a copolymer or terpolymer additive for controlling the rate of delivery of the therapeutic agent.
Inventor(s):	Cottone; Robert J. (Davie, FL)
Assignee:	OrbusNeich Medical, Inc. (Fort Lauderdale, FL)
Application Number:	11/875,887
Patent Claims:	1. An implantable medical device, comprising a crystallized bioabsorbable polymer scaffold and a coating; said crystallized bioabsorbable polymer scaffold comprising, at least about 70% (w/w) of a base polymer comprising a poly (L-lactide) moiety, and/or a poly (D-lactide) moiety, and/or poly L-lactide-co-PEG moiety, and/or poly D-lactide-co PEG moiety, linked with a modifying copolymer comprising poly (L-lactide-co-Tri-methylene-carbonate) or poly (D-lactide-co-tri-methylene-carbonate) or poly (L-lactide-co-.epsilon.-caprolactone) or poly (D-lactide-co-.epsilon.-caprolactone) in the form of block copolymers or blocky random copolymers; and said coating comprising a bioabsorbable matrix and a ligand. 2. The implantable medical device of claim 1 wherein said ligand is configured to bind target cells in vivo. 3. The implantable medical device of claim 1 wherein said ligand is a small molecule, a peptide, an antibody, antibody fragments, or combinations thereof and the target cell is a progenitor endothelial cell antigen. 4. The implantable medical device of claim 1 wherein said coating comprises one or more layers. 5. The implantable medical device of claim 1 wherein said matrix comprises a naturally occurring or synthetic biodegradable polymer. 6. The implantable medical device of claim 5 wherein said matrix comprises at least one of the group consisting of: tropoelastin, elastin, laminin, fibronectin, fibrin, collagen, basement membrane proteins, and cross-linked tropoelastin. 7. The implantable medical device of claim 4 wherein at least one coating layer, or the implantable medical device itself, comprises a radioopaque or radio-detectable material. 8. The implantable medical device of claim 1 wherein said implantable medical device is impregnated with a pharmacological or biological substance. 9. The implantable medical device of claim 1 comprising a tube defining a lumen, said tube having an outer surface and an inner surface, said inner surface surrounding said lumen. 10. The implantable medical device of claim 9 wherein said outer surface is coated with a composition comprising a pharmacological substance. 11. The implantable medical device of claim 9 wherein said outer or inner surface is coated with a composition comprising a biological substance. 12. The implantable medical device of claim 8 or 10 wherein said pharmacological substance is at least one of the group consisting of: cyclosporin A, mycophenolic acid, mycophenolate mofetil acid, rapamycin, rapamycin derivatives, biolimus A9, CCI-779, RAD 001, AP23573, azathioprene, pimecrolimus, tacrolimus (FK506), tranilast, dexamethasone, corticosteroid, everolimus, retinoic acid, vitamin E, rosglitazone, simvastatins, fluvastatin, estrogen, 17.beta.-estradiol, hydrocortisone, acetaminophen, ibuprofen, naproxen, fluticasone, clobetasol, adalimumab, sulindac, dihydroepiandrosterone, testosterone, puerarin, platelet factor 4, basic fibroblast growth factor, fibronectin, butyric acid, butyric acid derivatives, paclitaxel, paclitaxel derivatives, LBM-642, deforolimus, and probucol. 13. The implantable medical device of claim 11 wherein said biological substance is at least one of the group consisting of: antibiotics/antimicrobials, antiproliferative agents, antineoplastic agents, antioxidants, endothelial cell growth factors, smooth muscle cell growth and/or migration inhibitors, thrombin inhibitors, immunosuppressive agents, anti-platelet aggregation agents, collagen synthesis inhibitors, therapeutic antibodies, nitric oxide donors, antisense oligonucleotides, wound healing agents, therapeutic gene transfer constructs, peptides, proteins, extracelluar matrix components, vasodialators, thrombolytics, anti-metabolites, growth factor agonists, antimitotics, steroids, steroidal antiinflammatory agents, chemokines, proliferator-activated receptor-gamma agonists, proliferator-activated receptor-alpha agonists proliferator-activated receptor-beta agonists, proliferator-activated receptor-alpha/beta agonists, proliferator-activated receptor-delta agonists, NF.kappa.beta., proliferator-activated receptor-alpha-gamma agonists, nonsterodial antiinflammatory agents, angiotensin converting enzyme(ACE) inhibitors, free radical scavangers, inhibitors of the CX3CR1 receptor and anti-cancer chemotherapeutic agents. 14. The implantable medical device of claim 1, the crystallized bioabsorbable polymer scaffold comprises a base polymer of from about 70% by weight of poly (L-lactide) with 30% by weight of modifying copolymer poly L-lactice-co-TMC. 15. A bioabsorbable implant comprising: a crystallized bioabsorbable polymer scaffold comprising at least about 70% (w/w) of a base polymer comprising a poly (L-lactide) moiety, and/or a poly (D-lactide) moiety, and/or poly L-lactide-co-PEG moiety, and/or poly D-lactide-co PEG moiety, linked with a modifying copolymer comprising poly (L-lactide-co-Tri-methylene-carbonate) or poly (D-lactide-co-tri-methylene-carbonate) or poly (L-lactide-co-.epsilon.-caprolactone) or poly (D-lactide-co-.epsilon.-caprolactone) in the form of block copolymers or blocky random copolymers; and a ligand. 16. The bioabsorbable implant of claim 15, wherein the base polymer is 70% by weight of poly L-lactide with 30% by weight of modifying copolymer poly L-lactice-co-TMC. 17. The bioabsorbable implant of claim 15, wherein the ligand comprises a small molecule, a peptide, an antibody, antibody fragments, or combinations thereof and the target cell is a progenitor endothelial cell. 18. The bioabsorbable implant of claim 17, wherein the antibody or antibody fragments is specific for binding a progenitor endothelial cell membrane antigen. 19. The bioabsorbable implant of claim 18, wherein the progenitor endothelial cell membrane antigen is selected from the group consisting of CD34, CD45, CD133, CD14, CDw90, CD117, HLA-DR, VEGFR-1, VEGFR-2, CD146, CD130, CD131, stem cell antigen, stem cell factor 1, Tie-2, MCH-H-2Kk and MCH-HLA-DR. 20. The implantable medical device of claim 1, wherein said medical device comprises a bioabsorbable implant having a tissue contacting surface and a fluid contacting surface, said implant comprising a bioabsorbable, biocompatible first coating for controlled release of one or more pharmaceutical substances from said tissue contacting surface, and a second coating comprising one or more ligands which bind to specific molecules on cell membranes of progenitor endothelial cells on the fluid contacting surface of the medical device. 21. The bioabsorbable implant of claim 20, wherein the medical device is a stent, a vascular or other synthetic graft, or a stent in combination with a synthetic graft. 22. The bioabsorbable implant of claim 20, wherein the medical device is a vascular stent. 23. The bioabsorbable implant of claim 20, wherein the tissue contacting surface coating comprises poly(DL-lactide-co-glycolide) and one or more pharmaceutical substances. 24. The bioabsorbable implant of claim 20, wherein the tissue contacting surface coating comprises poly(DL-lactide), or poly(lactide-co-glycolide), and paclitaxel. 25. The bioabsorbable implant of claim 20, wherein the pharmaceutical substance is at least one of the group consisting of antibiotics/antimicrobials, antiproliferative agents, antineoplastic agents, antioxidants, endothelial cell growth factors, smooth muscle cell growth and/or migration inhibitors, thrombin inhibitors, immunosuppressive agents, anti-platelet aggregation agents, collagen synthesis inhibitors, therapeutic antibodies, nitric oxide donors, antisense oligonucleotides, wound healing agents, therapeutic gene transfer constructs, peptides, proteins, extracellular matrix components, vasodialators, thrombolytics, anti-metabolites, growth factor agonists, antimitotics, steroids, steroidal antiinflammatory agents, chemokines, proliferator-activated receptor-gamma agonists, proliferator-activated receptor-alpha-gamma agonists, proliferator-activated receptor-alpha agonists, proliferator-activated receptor-beta agonists, proliferator-activated receptor-alpha/beta agonists, proliferator-activated receptor-delta agonists, NF.kappa.beta., nonsterodial antiinflammatory agents, angiotensin converting enzyme(ACE) inhibitors, free radical scavangers, inhibitors of the CX3CR1 receptor, and anti-cancer chemotherapeutic agents. 26. The bioabsorbable implant of claim 20, wherein the pharmaceutical substance is selected from the group consisting of cyclosporin A, mycophenolic acid, mycophenolate mofetil acid, rapamycin, rapamycin derivatives, biolimus A9, CCI-779, RAD 001, AP23573, azathioprene, pimecrolimus, tacrolimus (FK506), tranilast, dexamethasone, corticosteroid, everolimus, retinoic acid, vitamin E, rosglitazone, simvastatins, fluvastatin, estrogen, 17.beta.-estradiol, hydrocortisone, acetaminophen, ibuprofen, naproxen, fluticasone, clobetasol, adalimumab, sulindac, dihydroepiandrosterone, testosterone, puerarin, platelet factor 4, basic fibroblast growth factor, fibronectin, butyric acid, butyric acid derivatives, paclitaxel, paclitaxel derivatives, LBM-642, deforolimus, and probucol. 27. The bioabsorbable implant of claim 24, wherein the poly(DL-lactide) polymer comprises from about 50 to about 99% of the composition. 28. The bioabsorbable implant of claim 20, wherein either or both coatings comprise multiple layers of the poly(DL-lactide) polymer, poly(lactide-co-glycolide) copolymer, or mixture thereof. 29. The bioabsorbable implant of claim 20, wherein the either or both coatings comprise multiple layers of the pharmaceutical substances.

Details for Patent 7,959,942

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Abbvie Inc.	HUMIRA	adalimumab	Injection	125057	12/31/2002		2026-10-20
Abbvie Inc.	HUMIRA	adalimumab	Injection	125057	02/21/2008		2026-10-20
Abbvie Inc.	HUMIRA	adalimumab	Injection	125057	04/24/2013		2026-10-20