Claims for Patent: 10,413,525

Summary for Patent: 10,413,525

Title:	Duloxetine sprinkles
Abstract:	The present invention relates in part a to multiparticulate sprinkle dosage form comprising duloxetine or a pharmaceutically acceptable salt thereof, having higher acid resistance as compared to commercially available delayed release formulations. It further relates to various methods of administering the said multiparticulate sprinkle dosage forms.
Inventor(s):	Agarwal; Ravindra (Udaipur, IN), Singhal; Tarun (Bharatpur, IN), Kochhar; Ravi (Haryana, IN)
Assignee:	Sun Pharmaceutical Industries Limited (Mumbai, Maharashtra, IN)
Application Number:	15/805,932
Patent Claims:	1. A multiparticulate sprinkle dosage form comprising a plurality of discrete units, wherein each unit comprises: (a) a core subunit comprising a drug layered subunit surrounding an inert core, wherein the drug layer comprises duloxetine or a pharmaceutically acceptable salt thereof; and (b) an enteric coating layer surrounding the core subunit; wherein each unit further comprises a finishing layer containing a cushioning agent, surrounding the enteric coating layer, wherein the cushioning agent is selected from the group consisting of polyethylene glycol, polyoxyethylene, polyvinyl acetate and gum; wherein not more than 90% of duloxetine is released from the dosage form when place in 40% ethanol in 0.1 NHCl for 2 hours. 2. The multiparticulate sprinkle dosage form according to claim 1, wherein the core subunit further comprises a sub-coating layer formed by a film forming agent selected from the group consisting of hydroxypropyl cellulose, hydroxypropylmethyl cellulose, and ethylcellulose. 3. The multiparticulate sprinkle dosage form according to claim 1, wherein the enteric coating layer comprises about 75% to about 99% by weight of an enteric polymer, based on the weight of the enteric coating. 4. The multiparticulate sprinkle dosage form according to claim 1, wherein the polyethylene glycol having a molecular weight of 6000 is present in an amount of about 2% to about 20% based on the total weight of the dosage form. 5. The multiparticulate sprinkle dosage form according to claim 1, wherein the dosage form contains duloxetine or pharmaceutically acceptable salts thereof in an amount of about 20% by weight of the dosage form. 6. The multiparticulate sprinkle dosage form according to claim 3, wherein the enteric polymer is selected from the group consisting of methacrylic acid copolymers, cellulose acetate phthalate, cellulose acetate succinate, polymethacrylic acid, hydroxypropyl methyl cellulose, hydroxypropyl methylcellulose phthalate, polyvinyl acetate phthalate, hydroxyethyl ethyl cellulose phthalate, cellulose acetate tetrahydrophthalate, acrylic resin, and mixtures thereof. 7. The multiparticulate sprinkle dosage form according to claim 1, wherein the discrete units are in the form selected from the group consisting of pellets, beads, particles, granules, and minitablets.