The invention provides compositions comprising bacterial strains for treating and preventing inflammatory and autoimmune diseases.

Disclosed are a compound, a stereisomer and a tautomer thereof, a pharmaceutically acceptable salt thereof, and a solvate or a prodrug thereof, which can be used for preventing or treating a RORγ mediated disease. The compound has the structural formula (I).

##STR00001##

The present invention discloses an antibody capable of binding to human interleukin 4 receptor alpha (hIL-4R alpha) and a preparation method and application thereof. The anti-hIL-4R alpha antibody can specifically bind to hIL-4R alpha, has good effects for inhibiting IL-4 and IL-13-induced cell line proliferation and the like, and can be applied to treatment of IL-4R alpha related diseases, such as immune-mediated inflammatory diseases.

Formulations comprising combinations of free amino acids useful for treating ARDS, asthma, or allergic rhinitis are described herein. Use of such amino acid formulations for treating ARDS, asthma, or allergic rhinitis in a subject in need thereof; in methods for treating ARDS, asthma, or allergic rhinitis in a subject in need thereof; and/or in the preparation of a medicament for the treatment of ARDS, asthma, or allergic rhinitis are encompassed herein.

Formulations comprising combinations of free amino acids useful for treating ARDS, asthma, or allergic rhinitis are described herein. Use of such amino acid formulations for treating ARDS, asthma, or allergic rhinitis in a subject in need thereof; in methods for treating ARDS, asthma, or allergic rhinitis in a subject in need thereof; and/or in the preparation of a medicament for the treatment of ARDS, asthma, or allergic rhinitis are encompassed herein.

The present invention relates to a medicament for treating various nervous system diseases or psychiatric diseases, comprising a compound of formula (1) or a pharmaceutically acceptable salt thereof as an active ingredient, wherein R.sup.1 is hydrogen, etc., R.sup.2 is halogen, etc., R.sup.3, R.sup.4, R.sup.5, and R.sup.6 are hydrogen, etc.

##STR00001##

An aqueous liquid preparation containing (+)-(S)-4-[4-[(4-chlorophenyl)(2-pyridyl)methoxy]piperidino]butyric acid or a pharmacologically acceptable acid addition salt thereof, which is stabilized with a water-soluble metal chloride, is provided.

The invention relates to new quinoxaline derivative compounds, to pharmaceutical compositions comprising said compounds, to processes for the preparation of said compounds and to the use of said compounds in the treatment of diseases, e.g. cancer.

Described herein are compounds that are inhibitors of autotaxin. Also described are pharmaceutical compositions and medicaments that include the compounds described herein, as well as methods of using such inhibitors, alone and in combination with other compounds, for treating autotaxin-dependent or autotaxin-mediated conditions or diseases.

There is provided a compound of formula (I) which is an inhibitor of the family of p38 mitogen-activated protein kinase enzymes, and to its use in therapy, including in pharmaceutical combinations, especially in the treatment of inflammatory diseases, including inflammatory diseases of the lung, such as asthma and COPD.