Abstract:
Polymorphs of Sunitinib malate and other salts have been prepared. Compositions comprising Sunitinib base, L-malic acid and another carboxylic acid are also described. Such polymorphs and compositions are useful, for example, in preparing pharmaceutical compositions.
Abstract:
Crystalline Vorinostat potassium salt form A characterized by a powder XRD pattern having peaks at about 4.9 and 7.4 ± 0.2 degrees 2-theta and any 3 peaks selected from the lis consisting of: 12.3, 19.8, 20.9, 22.1, 22.8, 28.7 and 29.5 ± 0.2 degrees 2-theta is provided. Crystalline Vorinostat potassium salt form A may be polymorphically pure. Processes for preparing crystalline Vorinostat potassium salt form A are also provided. Further provided i crystalline Vorinostat form VI characterized by a powder XRD pattern having peaks at about 14.3, 14.8, 17.6, 21.4 and 23.1 ± 0.2 degrees 2-theta as well as processes for preparing crystalline Vorinostat form VI.
Abstract:
Combinations of a pharmaceutically acceptable excipient selected from the group consisting of microcrystalline cellulose, polyvinylpyrrolidone, cyclodextrin, and disaccharide or derivatives thereof and acomposition of sunitinib base and L-malic acid were prepared.
Abstract:
The invention provides Sunitinib hemi-L-malate, polymorphs thereof, polymorphs of racemic sunitinib malate, compositions containing sunitinib base and either L or racemic malic acid, processes for the preparation thereof, and pharmaceutical compositions thereof.
Abstract:
The invention relates to solid state forms of Cabazitaxel and processes for preparing the solid state forms. The invention further relates to pharmaceutical compositions and formulations comprising one or more of the solid state forms.
Abstract:
The invention relates to solid state forms of Cabazitaxel, and processes for preparation, via novel synthetic intermediates, thereof, and formulations comprising one or more of the solid state forms of Cabazitaxel. The present invention further provides pharmaceutical compositions comprising one or more of the solid state forms of Cabazitaxel, and a method of treating hormone-refractory prostate cancer.
Abstract:
Novel polymorphs of Bendamustine HC1 have been prepared and characterized. These polymorphs and pharmaceutical compositions containing them are useful, for example, in treating patients with various cancers.
Abstract:
Combinations of a pharmaceutically acceptable excipient selected from the group consisting of microcrystalline cellulose, polyvinylpyrrolidone, cyclodextrin, and disaccharide or derivatives thereof and acomposition of sunitinib base and L-malic acid were prepared.
Abstract:
Provided is dasatinib, solvates thereof and their crystalline forms, methods for their preparation, and pharmaceutical compositions thereof. Formula (I).
Abstract:
The invention provides Sunitinib hemi-L-malate, polymorphs thereof, polymorphs of racemic sunitinib malate, compositions containing sunitinib base and either L or racemic malic acid, processes for the preparation thereof, and pharmaceutical compositions thereof.