Abstract:
The present invention provides for a method for the treatment of a respiratory disease, disorder or condition, or a viral infection or viral disease, disorder or condition in a subject, the method comprising the step of administering to said subject a medically active liquid in nebulized form by inhalation, wherein the medically active liquid comprises niclosamide or a pharmaceutically acceptable salt thereof and wherein the medically active liquid is administered in nebulized form using an inhalation device.
Abstract:
A formulation comprising an amount of niclosamide and one or more of a humectant, a lubricant, a solvent, an osmolality modulator, a pH modulator, a viscosity modulator, a preservative, or combinations thereof. Said formulation for use in promoting contraception, comprising administering an effective amount of the formulation to the subject, wherein, upon contacting a sperm cell, the formulation inhibits or decreases one or more of sperm motility, sperm viability, and sperm metabolism, thereby decreasing the probability of conception. A method of making said formulation, comprising: a) combining niclosamide with PEG-400 in a first vessel to form a solution; b) combining benzoic acid and/or benzyl alcohol with the solution of (a); c) combining water, sodium chloride, citric acid, lactic acid, potassium tartrate and carbopol 980 in a separate vessel to form an aqeous fraction; d) combining the aqueous fraction of (c) with the PEG fraction of (b); e) adding sodium hydroxide to the mixture of (d) to adjust the pH; f) optionally adding water to the mixture of (e); and g) mixing the mixture of (e) or (f) till a homogenous mixture is obtained.
Abstract:
The present invention relates to a compound for use in a method of treating a pathological condition selected from polycystic kidney disease, polycystic liver disease, and a combination thereof. The present invention further relates to a composition for use in a method of treating a pathological condition selected from polycystic kidney disease, polycystic liver disease, and a combination thereof.
Abstract:
The present invention relates to a new topical composition comprising niclosamide and/or oxyclozanide and to the use of said composition for the treatment or prevention of pyoderma or dermatitis in non-human mammals.
Abstract:
A dosage regimen for the topical prevention or treatment of a skin infection or an inflammatory skin condition in a human subject using a halogenated salicylanilide. The topical dosage regimen provides high concentrations of the halogenated salicylanilide in skin tissue which are retained for a prolonged period without the need for further topical dosing of the halogenated salicylanilide.
Abstract:
The invention discloses WNK signalling inhibitors, in particular closantel, for use in the prevention and treatment of disorders caused and/or characterized by elevated levels of serum fibroblast growth factor (FGF23), especially chronic kidney disease (CKD). The invention also provides pharmaceutical compositions comprising one/or more WNK signalling inhibitors and methods for use said pharmaceutical compositions in the treatment of subjects diagnosed with FGF23-associated disorders, wherein subjects may be humans and/or companion animals, e.g. dogs and cats.
Abstract:
Disclosed herein are methods of treating a malignant adrenocortical tumor, including a locally advanced and metastatic adrenocortical carcinoma. In some examples, methods of treating a malignant adrenocortical tumor include administering an effective amount of niclosamide alone or in combination with other therapeutic agents to a subject in need thereof, thereby treating the malignant adrenocortical tumor.
Abstract:
The present disclosure relates to methods for reducing the rate of cardiovascular death, myocardial infarction, or stroke in a patient in recognized need thereof, comprising administering to the patient a pharmaceutical composition comprising 60 mg ticagrelor twice daily.
Abstract:
The invention relates to the use of di-aspirin (bis(2-carboxyphenyl)succinate) and its derivatives in the treatment of colon and colorectal cancer. It also relates to novel derivatives of di-aspirin and to a method of synthesis of the di-aspirin and its derivatives.