Details for Patent: 9,744,170

Title:	Solid antiviral dosage forms
Abstract:	The present disclosure relates to solid dosage forms comprising antiviral compounds and methods of using such dosage forms to treat antiviral infection.
Inventor(s):	Miller; Jonathan M. (Lindenhurst, IL), Morris; John B. (Grayslake, IL), Sever; Nancy E. (Northbrook, IL), Schmitt; Eric A. (Libertyville, IL), Gao; Ping X. (Highland Park, IL), Shi; Yi (Libertyville, IL), Gao; Yi (Vernon Hills, IL), Liepold; Bernd (Dossenheim, DE), Moosmann; Anna (Winterbach, DE), Pauli; Mirko (Ludwigshafen, DE), Durak; Fatih (Ludwigshafen, DE), Kessler; Thomas (Schifferstadt, DE), Hoelig; Peter (Waechtersbach, DE), Rosenblatt; Karin (Mannheim, DE), Kostelac; Drazen (Mannheim, DE), Gokhale; Rajeev (Singapore, SG), Costello; Mark (Chicago, IL), Knable; Carl (Elmhurst, IL)
Assignee:	AbbVie Inc. (North Chicago, IL)
Filing Date:	Mar 18, 2016
Application Number:	15/073,767
Claims:	1. A solid dosage form comprising a first composition and a second composition, wherein: the first composition comprises from 40 mg to 180 mg of ##STR00011## from 5 mg to 30 mg of ##STR00012## from 25 mg to 120 mg of ritonavir, 70-85% by weight of copovidone; and 5% to 10% by weight of a pharmaceutically acceptable surfactant or a combination of pharmaceutically acceptable surfactants, wherein all percentages are weight percentages relative to the total weight of the first composition, and wherein Compound 1, Compound 2 and ritonavir are formulated in an amorphous solid dispersion; the second composition comprises from 75 mg to 900 mg (free acid equivalent) of a sodium monohydrate salt of ##STR00013## 20-40% copovidone, and 20-40% hypromellose, wherein all percentages are weight percentages relative to the total weight of the second composition; when dissolved in 900 mL of a dissolution medium using a standard USP dissolution Apparatus 2 (paddle) operating at 100 RPM at 37.degree. C., 50-60% Compound 1 in the solid dosage form is released within 1 hour, 50-60% Compound 2 in the solid dosage form is released within 1 hour, 50-60% ritonavir in the solid dosage form is released within 1 hour, and 0.5-2% Compound 4 in the solid dosage form is released within 1 hour, wherein the dissolution medium is 0.05 M sodium phosphate buffer (pH 6.8) with 15 mM cetyltrimethylammonium bromide (cTAB), and the total weight of the solid dosage form is from 1000 mg to 1600 mg. 2. The solid dosage form of claim 1, wherein the first composition comprises from 45 mg to 55 mg of Compound 1, from 7.5 mg to 9.5 mg of Compound 2, and from 30 mg to 37 mg of ritonavir, and the second composition comprises from 150 mg to 300 mg (free acid equivalent) of the sodium monohydrate salt of Compound 4. 3. A method for treating hepatitis C virus (HCV) infection in a patient in need of such treatment, wherein the method comprises administering once daily to the patient at least one solid dosage form of claim 1. 4. A method for treating HCV infection in a patient in need of such treatment, wherein the method comprises administering once daily to the patient three solid dosage forms of claim 1. 5. A solid dosage form comprising a first composition and a second composition, wherein: the first composition comprises from 40 mg to 180 mg of Compound 1, from 5 mg to 30 mg of Compound 2, from 25 mg to 120 mg of ritonavir, 70-85% by weight of copovidone; and 5% to 10% by weight of a pharmaceutically acceptable surfactant or a combination of pharmaceutically acceptable surfactants, wherein all percentages are weight percentages relative to the total weight of the first composition, and wherein Compound 1, Compound 2 and ritonavir are formulated in an amorphous solid dispersion; the second composition comprises from 75 mg to 900 mg (free acid equivalent) of a sodium monohydrate salt of Compound 4, 20-40% copovidone, and 20-40% hypromellose, wherein all percentages are weight percentages relative to the total weight of the second composition; when dissolved in 900 mL of a dissolution medium using a standard USP dissolution Apparatus 2 (paddle) operating at 100 RPM at 37.degree. C., 95-100% Compound 1 in the solid dosage form is released within 4 hours, 95-100% Compound 2 in the solid dosage form is released within 4 hours, 95-100% ritonavir in the solid dosage form is released within 4 hours, and 10-15% Compound 4 in the solid dosage form is released within 4 hours, wherein the dissolution medium is 0.05 M sodium phosphate buffer (pH 6.8) with 15 mM cTAB, and the total weight of the solid dosage form is from 1000 mg to 1600 mg. 6. The solid dosage form of claim 5, wherein the first composition comprises from 45 mg to 55 mg of Compound 1, from 7.5 mg to 9.5 mg of Compound 2, and from 30 mg to 37 mg of ritonavir, and the second composition comprises from 150 mg to 300 mg (free acid equivalent) of the sodium monohydrate salt of Compound 4. 7. A method for treating HCV infection in a patient in need of such treatment, wherein the method comprises administering once daily to the patient at least one solid dosage form of claim 5. 8. A method for treating HCV infection in a patient in need of such treatment, wherein the method comprises administering once daily to the patient three solid dosage forms of claim 5. 9. A solid dosage form comprising a first composition and a second composition, wherein: the first composition comprises from 40 mg to 180 mg of Compound 1, from 5 mg to 30 mg of Compound 2, from 25 mg to 120 mg of ritonavir, 70-85% by weight of copovidone; and 5% to 10% by weight of a pharmaceutically acceptable surfactant or a combination of pharmaceutically acceptable surfactants, wherein all percentages are weight percentages relative to the total weight of the first composition, and wherein Compound 1, Compound 2 and ritonavir are formulated in an amorphous solid dispersion; the second composition comprises from 75 mg to 900 mg (free acid equivalent) of a sodium monohydrate salt of Compound 4, 20-40% copovidone, and 20-40% hypromellose, wherein all percentages are weight percentages relative to the total weight of the second composition; when dissolved in 900 mL of a dissolution medium using a standard USP dissolution Apparatus 2 (paddle) operating at 100 RPM at 37.degree. C., 95-100% Compound 1 in the solid dosage form is released within 6 hours, 95-100% Compound 2 in the solid dosage form is released within 6 hours, 95-100% ritonavir in the solid dosage form is released within 6 hours, and 15-20% Compound 4 in the solid dosage form is released within 6 hours, wherein the dissolution medium is 0.05 M sodium phosphate buffer (pH 6.8) with 15 mM cTAB, and the total weight of the solid dosage form is 1000 mg to 1600 mg. 10. The solid dosage form of claim 9, wherein the first composition comprises from 45 mg to 55 mg of Compound 1, from 7.5 mg to 9.5 mg of Compound 2, and from 30 mg to 37 mg of ritonavir, and the second composition comprises from 150 mg to 300 mg (free acid equivalent) of the sodium monohydrate salt of Compound 4. 11. A method for treating HCV infection in a patient in need of such treatment, wherein the method comprises administering once daily to the patient at least one solid dosage form of claim 9. 12. A method for treating HCV infection in a patient in need of such treatment, wherein the method comprises administering once daily to the patient three solid dosage forms of claim 9. 13. A solid dosage form comprising a first composition and a second composition, wherein: the first composition comprises from 40 mg to 180 mg of Compound 1, from 5 mg to 30 mg of Compound 2, from 25 mg to 120 mg of ritonavir, 70-85% by weight of copovidone; and 5% to 10% by weight of a pharmaceutically acceptable surfactant or a combination of pharmaceutically acceptable surfactants, wherein all percentages are weight percentages relative to the total weight of the first composition, and wherein Compound 1, Compound 2 and ritonavir are formulated in an amorphous solid dispersion; the second composition comprises from 75 mg to 900 mg (free acid equivalent) of a sodium monohydrate salt of Compound 4, 20-40% copovidone, and 20-40% hypromellose, wherein all percentages are weight percentages relative to the total weight of the second composition; when dissolved in 900 mL of a dissolution medium using a standard USP dissolution Apparatus 2 (paddle) operating at 100 RPM at 37.degree. C., 100% Compound 1 in the solid dosage form is released within 8 hours, 100% Compound 2 in the solid dosage form is released within 8 hours, 100% ritonavir in the solid dosage form is released within 8 hours, 20-30% Compound 4 in the solid dosage form is released within 8 hours, 30-40% Compound 4 in the solid dosage form is released within 12 hours, and 40-60% Compound 4 in the solid dosage form is released within 16 hours, wherein the dissolution medium is 0.05 M sodium phosphate buffer (pH 6.8) with 15 mM cTAB, and the total weight of the solid dosage form is from 1000 mg to 1600 mg. 14. The solid dosage form of claim 13, wherein the first composition comprises from 45 mg to 55 mg of Compound 1, from 7.5 mg to 9.5 mg of Compound 2, and from 30 mg to 37 mg of ritonavir, and the second composition comprises from 150 mg to 300 mg (free acid equivalent) of the sodium monohydrate salt of Compound 4. 15. A method for treating HCV infection in a patient in need of such treatment, wherein the method comprises administering once daily to the patient at least one solid dosage form of claim 13. 16. A method for treating HCV infection in a patient in need of such treatment, wherein the method comprises administering once daily to the patient three solid dosage forms of claim 13. 17. A solid dosage form comprising a first composition and a second composition, wherein: the first composition comprises from 40 mg to 180 mg of Compound 1, from 5 mg to 30 mg of Compound 2, from 25 mg to 120 mg of ritonavir, 70-85% by weight of copovidone; and 5% to 10% by weight of a pharmaceutically acceptable surfactant or a combination of pharmaceutically acceptable surfactants, wherein all percentages are weight percentages relative to the total weight of the first composition, and wherein Compound 1, Compound 2 and ritonavir are formulated in an amorphous solid dispersion; the second composition comprises from 75 mg to 900 mg (free acid equivalent) of a sodium monohydrate salt of Compound 4, 20-40% copovidone, and 20-40% hypromellose, wherein all percentages are weight percentages relative to the total weight of the second composition; when dissolved in 900 mL of a dissolution medium using a standard USP dissolution Apparatus 2 (paddle) operating at 100 RPM at 37.degree. C., 100% Compound 1 in the solid dosage form is released within 8 hours, 100% Compound 2 in the solid dosage form is released within 8 hours, 100% ritonavir in the solid dosage form is released within 8 hours, 20-30% Compound 4 in the solid dosage form is released within 8 hours, 30-40% Compound 4 in the solid dosage form is released within 12 hours, 40-60% Compound 4 in the solid dosage form is released within 16 hours, and 60-80% Compound 4 in the solid dosage form is released within 24 hours, wherein the dissolution medium is 0.05 M sodium phosphate buffer (pH 6.8) with 15 mM cTAB, and the total weight of the solid dosage form is from 1000 mg to 1600 mg. 18. The solid dosage form of claim 17, wherein the first composition comprises from 45 mg to 55 mg of Compound 1, from 7.5 mg to 9.5 mg of Compound 2, and from 30 mg to 37 mg of ritonavir, and the second composition comprises from 150 mg to 300 mg (free acid equivalent) of the sodium monohydrate salt of Compound 4. 19. A method for treating HCV infection in a patient in need of such treatment, wherein the method comprises administering once daily to the patient at least one solid dosage form of claim 17. 20. A method for treating HCV infection in a patient in need of such treatment, wherein the method comprises administering once daily to the patient three solid dosage forms of claim 17.