Claims for Patent: 12,109,193

Summary for Patent: 12,109,193

Title:	Spray-dried dispersions, formulations, and polymorphs of (s)-5-amino-3-(4-((5-fluoro-2-methoxybenzamido)methyl)phenyl)-1-(1,1,1-trifluoropropan-2-yl)-1H-pyrazole-4-carboxamide
Abstract:	A spray-dried dispersions and pharmaceutical composition of (S)-5-amino-3-(4-((5-fluoro-2-methoxybenzamido)methyl)phenyl)-1-(1,1,1-trifluoropropan-2-yl)-1H-pyrazole-4-carboxamide, pharmaceutically acceptable salts thereof, or a combination thereof and the use of the spray-dried dispersion and pharmaceutical composition in the treatment of cancer and autoimmune and inflammatory diseases are disclosed. Also provided are crystalline forms of (S)-5-amino-3-(4-((5-fluoro-2-methoxy-benzamido)methyl)phenyl)-1-(1,1,1-trifluoropropan-2-yl)-1H-pyrazole-4-carboxamide also useful in the treatment of cancer and autoimmune and inflammatory diseases.
Inventor(s):	Barbara J. Brandhuber, Lauren T. Brent, Charles Todd Eary, Andrew Kenna, Firas Khan, Vivian F. H. Renshaw, Stacey Renee Spencer
Assignee:	Loxo Oncology Inc
Application Number:	US17/260,745
Patent Claims:	1. A pharmaceutical composition comprising a spray-dried dispersion comprising a compound of Formula I: or a pharmaceutically acceptable salt thereof and one or more polymers selected from the group consisting of an HPMCAS polymer, an HPMC polymer, a vinylpyrrolidone-vinyl acetate copolymer, and a polyvinylpyrrolidone (PVP) polymer and a pharmaceutically acceptable excipient. 2. The pharmaceutical composition of claim 1, wherein the compound of Formula I or a pharmaceutically acceptable salt thereof and the HPMCAS polymer are present in a ratio of about 1:1; microcrystalline cellulose is present in an amount between about 30% w/w and about 60% w/w; lactose monohydrate is present in an amount between about 10% w/w and about 60% w/w; croscarmellose sodium is present in an amount between about 0.5% w/w and about 5% w/w; magnesium stearate is present in an amount between about 0.05% w/w and about 2% w/w; and silicon dioxide in an amount between about 0.3% w/w and about 0.6% w/w, when present, and wherein the spray-dried dispersion is present in the pharmaceutical tablet composition in an amount between about 40% w/w and about 50% w/w. 3. The pharmaceutical composition according to claim 1, wherein the one or more polymers is an HPMCAS polymer. 4. The pharmaceutical composition according to claim 1 or 3, wherein the HPMCAS polymer is one or more of HPMCAS-MG, HPMCAS-LF, HPMCAS-LG, HPMCAS-MF, HPMCAS-HF, or HPMCAS-HG. 5. The pharmaceutical composition according to claim 4, wherein the HPMCAS polymer is HPMCAS-MG. 6. The pharmaceutical composition according to claim 4, further comprising a coating.