Stabilized pharmaceutical composition
Provided is a pharmaceutical composition, which comprises 5-{[(3R)-1-acryloylpyrrolidin-3-yl]oxy}-6-ethyl-3-({4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl}amino)-pyrazine-2-carboxamide (hereinafter referred to as “compound A”) or a pharmaceutically acceptable salt thereof, and is stabilized. The pharmaceutical composition comprises compound A or a pharmaceutically acceptable salt thereof, and a pharmaceutical additive having a difference in water activity value of 0.1 or more, and is stabilized.
1. A pharmaceutical composition, comprising 5-{[(3R)-1-acryloylpynolidin-3-yl]oxy}-6-ethyl-3-({4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl}amino)-pyrazine-2-carboxamide, or a pharmaceutically acceptable salt thereof, and a pharmaceutical additive having a difference in water activity value of 0.1 or more, wherein the difference in water activity value is the water activity value difference between said pharmaceutical additive after storage in the opened state and said pharmaceutical additive after storage in the sealed state, and wherein the pharmaceutical additive having a difference in water activity value of 0.1 or more is one member, or two or more members selected from the group consisting of dextran, dextrin, crystalline cellulose, corn starch, calcium carbonate, lactose hydrate, anhydrous dibasic calcium phosphate, and mannitol.
2. The pharmaceutical composition according to claim 1 , wherein the pharmaceutical additive having a difference in water activity value of 0.1 or more is lactose hydrate.
3. The pharmaceutical composition according to claim 1 , wherein lactose hydrate is one member, or two or more members selected from the group consisting of sieved lactose, milled lactose, spray-dried lactose, and granulated lactose.
4. The pharmaceutical composition according to claim 1 , wherein lactose hydrate is spray-dried lactose.
5. The pharmaceutical composition according to claim 1 , wherein the content of the pharmaceutical additive having a difference in water activity value of 0.1 or more is about 0.1% by weight to about 99.9% by weight with respect to the weight of the pharmaceutical composition.
6. The pharmaceutical composition according to claim 1 , wherein the water activity of the pharmaceutical composition is controlled.
7. The pharmaceutical composition according to claim 1 , wherein the pharmaceutical composition is a capsule.
8. The pharmaceutical composition according to claim 1 , wherein the increased amount of a related substance of 5-{[(3R)-1-acryloylpyrrolidin-3-yl]oxy}-6-ethyl-3-({4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl}amino)-pyrazine-2-carboxamide, or a pharmaceutically acceptable salt thereof is 0.05% or less.
9. A method of stabilizing a pharmaceutical composition comprising 5-{[(3R)-1-acryloylpyrrolidin-3-yl]oxy}-6-ethyl-3-({4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl}amino)-pyrazine-2-carboxamide, or a pharmaceutically acceptable salt thereof, by using a pharmaceutical additive having a difference in water activity value of 0.1 or more, wherein the difference in water activity value is the water activity value difference between said pharmaceutical additive after storage in the opened state and said pharmaceutical additive after storage in the sealed state, and wherein the pharmaceutical additive having a difference in water activity value of 0.1 or more is one member, or two or more members selected from the group consisting of dextran, dextrin, crystalline cellulose, corn starch, calcium carbonate, lactose hydrate, anhydrous dibasic calcium phosphate, and mannitol.
10. A pharmaceutical composition comprising 5-{[(3R)-1-acryloylpyrrolidin-3-yl]oxy }-6-ethyl-3-({4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl}amino)-pyrazine-2-carboxamide, or a pharmaceutically acceptable salt thereof, and lactose.
11. The pharmaceutical composition according to claim 1 , wherein the pharmaceutical additive having a difference in water activity value of 0.1 or more is one member, or two or more members selected from the group consisting of dextran, dextrin, and anhydrous dibasic calcium phosphate.
12. The method of stabilizing a pharmaceutical composition of claim 9 , wherein the pharmaceutical additive having a difference in water activity value of 0.1 or more is one member, or two or more members selected from the group consisting of dextran, dextrin, and anhydrous dibasic calcium phosphate.