Abstract:
Crystalline lestaurtinib hydrates and crystalline lestaurtinib hemihydrate hemicetonitrileate and crystalline lestaurtinib hemihydrate hemitetrahydrofuranate, processes to reproducibly make them and methods of treating patients using them are disclosed.
Abstract:
The present invention relates to a pharmaceutical composition and concentrate suitable for oral administration comprising a hydrophilic drug solubilized in a lipophilic phase comprising a fatty acid, and water; an oral formulation comprising uniform dispersion of the pharmaceutical concentrate in an aqueous phase optionally comprising a self-emulsifying material; and to a process of making the same.
Abstract:
Lestaurtinib Crystalline Form 1, isolated crystalline lestaurtinib anhydrate and amorphous lestaurtinib, processes to reproducibly make them and methods of treating patients using them.
Abstract:
Crystalline lestaurtinib hydrates and crystalline lestaurtinib hemihydrate hemicetonitrileate and crystalline lestaurtinib hemihydrate hemitetrahydrofuranate, processes to reproducibly make them and methods of treating patients using them are disclosed.
Abstract:
La presente invencion se refiere a la forma cristalina 2 del clorhidrato de atrasentan, a composiciones que la contienen, y a metodos de tratamiento de enfermedades e inhibicion de reacciones fisiologicas adversas, utilizandola.