Extended release tablet formulations of flibanserin and method for manufacturing the same
The present invention provides pharmaceutical release systems comprising an therapeutically effective amount of flibanserin and at least one pharmaceutically acceptable excipient, characterized in that said pharmaceutical release systems exhibit a pharmacokinetic profile that is characterized by an average maximum flibanserin plasma concentration C max lower than 300 ng/mL, preferably lower than 200 ng/mL after administration of a single dose to healthy volunteers in fasted state or directly after a meal.
1. A pharmaceutical release system comprising:
(a) a therapeutically effective amount of flibanserin, or pharmaceutically acceptable salt thereof,
(b) a pharmaceutically acceptable pH-dependent polymer;
(c) a pharmaceutically acceptable pH-independent polymer; and
(d) a pharmaceutically acceptable acid,
wherein the composition exhibits a pharmacokinetic profile that is characterized by an average maximum flibanserin plasma concentration C max of less than 300 ng/mL and an average total systemic exposure between 1300 and 3000 ng·h/mL after administration of a single daily dose to healthy volunteers in fasted state or directly after a meal.
2. The pharmaceutical release system according to claim 1 , characterized by an average maximum flibanserin plasma concentration C max of less than 300 ng/mL and an average total systemic exposure between 1500 and 2500 ng·h/mL after administration of a single daily dose to healthy volunteers in fasted state or directly after a meal.
3. The pharmaceutical release system according to claim 1 , characterized by having an in vitro dissolution profile such that at least 1% w/w and no more than 60% w/w of the flibanserin is released at 1 hour; at least 5% w/w and up to 70% w/w of the flibanserin is released at 4 hours; at least 30% w/w and up to 100% w/w of the flibanserin is released at 12 hours, when dissolution is measured using a USP (Type II) apparatus.
4. The pharmaceutical release system according to claim 2 , characterized by having an in vitro dissolution profile such that at least 1% w/w and no more than 60% w/w of the flibanserin is released at 1 hour; at least 5% w/w and up to 70% w/w of the flibanserin is released at 4 hours; at least 30% w/w and up to 100% w/w of the flibanserin is released at 12 hours, when dissolution is measured using a USP (Type II) apparatus.
5. The pharmaceutical release system according to claim 1 , characterized by having an in vitro dissolution profile such that at least 1% w/w and no more than 50% w/w of the flibanserin is released at 1 hour; at least 5% w/w and up to 60% w/w of the flibanserin is released at 4 hours; at least 35% w/w and up to 95% w/w of the flibanserin is released at 12 hours, when dissolution is measured using a USP (Type II) apparatus.
6. The pharmaceutical release system according to claim 2 , characterized by having an in vitro dissolution profile such that at least 1% w/w and no more than 50% w/w of the flibanserin is released at 1 hour; at least 5% w/w and up to 60% w/w of the flibanserin is released at 4 hours; at least 35% w/w and up to 95% w/w of the flibanserin is released at 12 hours, when dissolution is measured using a USP (Type II) apparatus.