Claims for Patent: 10,130,582

Summary for Patent: 10,130,582

Title:	Complexes of abiraterone acetate, process for the preparation thereof and pharmaceutical compositions containing them
Abstract:	The present disclosure relates to pharmaceutically acceptable complex formulae comprising complexes of Abiraterone acetate and pharmaceutically acceptable excipients, process for the preparation thereof and pharmaceutical compositions containing them. The complex formulae of the present disclosure have improved physicochemical properties which results in reduced food effect which allows significant dose reduction and the abandoning of the requirement of taking the drug on an empty stomach.
Inventor(s):	Angi; Reka (Nagykovacsi, HU), Jordan; Tamas (Ocsod, HU), Basa-Denes; Orsolya (Eger, HU), Solymosi; Tamas (Bekescsaba, HU), Otvos; Zsolt (Csongrad, HU), Glavinas; Hristos (Szeged, HU), Filipcsei; Genoveva (Budapest, HU)
Assignee:	Druggability Technologies IP Holdco Limited (Msida, MT)
Application Number:	15/456,988
Patent Claims:	1. A stable complex with improved physicochemical characteristics and enhanced biological performance comprising a) Abiraterone acetate; b) at least one complexing agent chosen from polyvinylcaprolactam-polyvinyl acetate-polyethylene-glycol graft copolymers; poloxamers; polyvinylpyrrolidone; copolymers of vinylpyrrolidone and vinyl-acetate; and poly(maleic acid-co-methyl-vinyl-ether); and c) a pharmaceutically acceptable excipient is sodium deoxycholate (SDC); wherein said complex is obtained via continuous flow mixing process; wherein said complex has a particle size less than 600 nm, and possesses one or more among the following features: a) it is instantaneously redispersible in physiological relevant media; b) it has increased dissolution rate compared to Zytiga; c) it is stable in solid form and in colloid solution and/or dispersion; d) its apparent solubility in water is of at least 0.6 mg/mL; e) it has a parallel artificial membrane permeability assay (PAMPA) permeability of at least 0.5.times.10.sup.-6 cm/s when dispersed in distilled water, which does not decrease in time at least for 3 months; f) exhibits no positive food effect (fed/fasted ratio is under 1.25) which allows significant dose reduction and the abandoning of the requirement of taking the drug on an empty stomach; and g) the variability of exposure is significantly reduced when compared to Zytiga. 2. The complex as recited in claim 1, wherein said complex has a particle size in the range between 100 nm and 500 nm. 3. The complex as recited in claim 1, wherein said complex exhibits X-ray amorphous character in the solid form. 4. The complex as recited in claim 1, wherein said complex possesses at least two of the properties described in a)-g). 5. The complex as recited in claim 4, wherein said complex possesses at least three of the properties described in a)-g). 6. The complex as recited in claim 4, wherein said complex has an apparent solubility in water of at least 0.6 mg/mL and exhibits no positive food effect which allows significant dose reduction and the abandoning of the requirement of taking the drug on an empty stomach. 7. The complex as recited in claim 4, wherein said complex has a parallel artificial membrane permeability assay (PAMPA) permeability of at least 0.5.times.10.sup.-6 cm/s and exhibits no positive food effect which allows significant dose reduction and the abandoning of the requirement of taking the drug on an empty stomach. 8. The complex as recited in claim 4, wherein said complex has an apparent solubility in water of at least 0.6 mg/mL and a PAMPA permeability of at least 0.5.times.10.sup.-6 cm/s. 9. The complex as recited in claim 5, wherein said complex has an apparent solubility in water of at least 0.6 mg/mL, PAMPA permeability of at least 0.5.times.10.sup.-6 cm/s, and exhibits no positive food effect which allows significant dose reduction and the abandoning of the requirement of taking the drug on an empty stomach. 10. The complex as recited in claim 1, wherein said complex is composed of a) 5 to 40% by weight of Abiraterone acetate; b) 5 to 80% by weight of a complexing agent; c) 0.1 to 50% by weight of a pharmaceutically acceptable excipient. 11. The complex as recited in claim 1, wherein said complex further comprises one or more additional active agent selected from the group consisting of Rifampicin, Prednisone/Prednisolone, Dexamethasone, Ketoconazole, Testosterone Enanthate, Enzalutamide, Dextromethorphan hydrobromide, Dexamethasone, Exemestane, Goserelin, Degarelix, Veliparib, Dovitinib, Leuprolide, Alisertib, cabozantinib, Cabazitaxel, Dasatinib, Glucocorticoid, Docetaxel, Dutasteride, Hydroxychloroquine, Ipilimumab, Metformin, Sunitinib, Selinexor, Everolimus, Trastuzumab, Tamoxifen, and combinations thereof. 12. A pharmaceutical composition comprising the stable complex as recited in claim 1 together with a pharmaceutically acceptable carrier. 13. The pharmaceutical composition as recited in claim 12, wherein said composition is suitable for oral administration. 14. The pharmaceutical composition as recited in claim 13 for use for the treatment of early stage or metastatic prostate cancer or advanced breast cancer.

Details for Patent 10,130,582

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	09/25/1998		2035-02-09
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	02/10/2017		2035-02-09
Bristol-myers Squibb Company	YERVOY	ipilimumab	Injection	125377	03/25/2011		2035-02-09