The present application relates to an agonist of a human kisspeptin receptor for use in a method of treating a disorder of sexual desire in human females, a method of treating a disorder of sexual desire in a human female patient, comprising administering to said patient a therapeutically effective amount of an agonist of a human kisspeptin receptor and a non-therapeutic method of enhancing libido or inducing sexual arousal in a human female subject, comprising administering to said subject an amount of an agonist of a human kisspeptin receptor sufficient to enhance libido in said subject.

The development of a superior GLP-1 secretion-promoting component is expected. The present invention provides a GLP-1 secretion-promoting composition comprising a GLP-1 secretion-promoting component and an emulsified particle that contains an oil-in-water emulsifying agent.

The development of a superior GLP-1 secretion-promoting component is expected. The present invention provides a GLP-1 secretion-promoting composition comprising a GLP-1 secretion-promoting component and an emulsified particle that contains an oil-in-water emulsifying agent.

The present invention provides oligopeptides, in particular, Ang-(1-7) derivatives, and methods for using and producing the same. In one particular embodiment, oligopeptides of the invention have higher blood-brain barrier penetration and/or in vivo half-life compared to the native Ang-(1-7), thereby allowing oligopeptides of the invention to be used in a wide variety of clinical applications including in treatment of cognitive dysfunction and/of impairment.

The present invention provides oligopeptides, in particular, Ang-(1-7) derivatives, and methods for using and producing the same. In one particular embodiment, oligopeptides of the invention have higher blood-brain barrier penetration and/or in vivo half-life compared to the native Ang-(1-7), thereby allowing oligopeptides of the invention to be used in a wide variety of clinical applications including in treatment of cognitive dysfunction and/of impairment.

This invention provides a method of colonic cleansing.

This invention provides a method of colonic cleansing.

This invention provides a method of colonic cleansing.

Field of application: The invention relates to medicine and pharmacy and allows to obtain new pharmaceutical compositions based on polymyxin for the treatment of severe infectious diseases, but not possessing nephrotoxic properties in therapeutic doses. Technical result: New combined dosage forms based on the antibiotic polymyxin with low nephrotoxicity and high activity.

Provided herein are beta-TCP binding sequences and chimeric polypeptides that include one or more beta-TCP binding sequences and a mammalian growth factor, compositions comprising any of these chimeric polypeptides (and optionally, beta-TCP), and methods of promoting bone or cartilage formulation, methods of replacing and/or repairing bone or cartilage, and methods of treating a bone fraction or bone loss that include administration of any of these compositions.