摘要:
A pharmaceutical composition comprising a compound of formula (I), or a pharmaceutically-acceptable salt or ester thereof in which X, R , R , R , R , R and R have the meanings given in the specification, is useful in the treatment of diseases of the central nervous system. The invention further relates to a compound of formula (I) or a pharmaceutically-acceptable salt or ester thereof useful in the treatment of diseases of the central nervous system.
摘要翻译:一种药物组合物,其包含式(I)化合物或其药学上可接受的盐或酯,其中X,R 1,R 2,R 3,R 4,R 5和 R 6具有说明书中给出的含义,可用于治疗中枢神经系统疾病。 本发明还涉及可用于治疗中枢神经系统疾病的式(I)化合物或其药学上可接受的盐或酯。
摘要:
Chemical engines and processes for their use and construction are described. The chemical engines can provide powerful and compact devices, especially autoinjectors for the rapid, powered injection of viscous medicines. Novel formulations and designs of chemical engines and delivery technologies employing the chemical engines are described.
摘要:
Provided are analgesic compounds, and salts thereof, of formula: ( I ) wherein A is: ( A ) Additionally, pharmaceutical formulations and methods of use employing the above compounds are provided.
摘要:
The present invention relates to altering the concentration of fibrinogen, specifically, for example, by decreasing fibrinogen concentration. The present invention also relates to methods for improving the cardiovascular risk profile of a subject by decreasing fibrinogen concentration.
摘要:
An improved method for treating gastric cancer, ovarian cancer, non-small cell lung cancer, or colorectal cancer in a patient is described, as well as pharmaceutical compositions useful for the method and a process for preparing said compositions.
摘要:
The present invention is directed to compounds of the structural Formula: wherein: R1 is H or -C1-C3 alkyl; R2 is selected from the group consisting of -H, -C1-C4 alkyl, -C1-C3 alkyl-CF3, phenyl, and pyridinyl; and R3 is selected from the group consisting of -H, -C1-C4 alkyl, -C1-C3 alkyl-O-CH3, -CH2-cyclopropyl, -CH2-C=CH2, -CH2CH2-(2-F-phenyl), and phenyl substituted with from 1 to 2 fluorines; provided that when R1 and R2 are each H, then R3 is selected from the group consisting of -C1-C4 alkyl, -C1-C3 alkyl-O-CH3, -CH2-cyclopropyl, -CH2-C=CH2, -CH2CH2-(2-F-phenyl), and phenyl substituted with from 1 to 2 fluorines; or stereoisomers and pharmaceutically acceptable salts thereof.
摘要:
The present invention provides very high affinity antibodies, or antigen-binding fragments thereof, that neutralize mature human TGF-ßl, TGF-ß2, and TGF-ß3. The antibodies of the invention are useful for treating cell proliferative disorders in a mammal.
摘要:
The present invention discloses novel compounds of Formula (I): having 11ß-HSD type 1 antagonist activity, as well as methods for preparing such compounds. In another embodiment, the invention discloses pharmaceutical compositions comprising compounds of Formula I, as well as methods of using the compounds and compositions to treat diabetes, hyperglycemia, obesity, hypertension, hyperlipidemia, metabolic syndrome, and other conditions associated with 11ß-HSD type 1 activity.
摘要:
A fluid injecting device (30) generally including a fluid delivery assembly (32) and a needle-free injecting assembly (34). The fluid delivery assembly (32) delivers or transfers the fluid medicine from a cartridge (40) into the needle-free injecting assembly (34) for injecting into a patient. A drive train (112) applies a force to a piston (64) inside the cartridge (40) during the delivery of the fluid to the needle-free injecting assembly (34) to prevent adhesion or static friction between the piston (64) and the cartridge (40). In addition, sensors can be used to help ensure the proper amount of dosage is transferred to the needle-free injecting assembly, conserve power, reduce leakage during disassembly, among other functions.