Active substance combination for systemic treatment of inflammation and malicious disorders
The present invention relates to a combination of two natural and a semi-synthetic active ingredient, and to a pharmaceutical composition thereof.
The present invention relates to a combination of two natural and a semi-synthetic active ingredient, and to a pharmaceutical composition thereof.
The present invention relates to a newly isolated strain of PPV1. The invention further relates to the use of the novel strain PPV1 for eliciting an immune response. The invention further relates to the use of the new strain PPV1 for the preparation of vaccine compositions.
Porcine parvovirus 2 (PPV2) is a member of a recently discovered worldwide group of porcine parvoviruses and is often detected in the background of respiratory symptoms, suggesting a pathological role for the virus in the disease.
The invention relates to a compound having an oxime moiety or a pharmaceutically acceptable salt, hydrate or solvate thereof and its use for inhibiting semicarbazide-sensitive amine oxidase (SSAO), also known as vascular adhesion protein- 1 (VAP-I), a pharmaceutical composition comprising the compound or a salt, hydrate or solvate thereof as an active ingredient, a method for the prevention or the treatment of a SSAO/VAP-1 related disease, said diseases including acute or chronic inflammatory diseases, diseases related to carbohydrate metabolism, diabetes-associated complications, diabetic retinopathy and macular oedema, diseases related to adipocyte or smooth muscle dysfunctions, neurodegenerative diseases and vascular diseases.
The present invention is directed to kynurenic acid amide analogues as well as salts thereof, to pharmaceutical compositions containing said compounds for use for curing the symptoms of Huntingtons’s disease as well as for preventing the development of said symptoms.