Method and composition for treatment of acne vulgaris

This invention relates to an improved method and composition for controlling all grades of acne vulgaris using a combination of sodium in the form of a pharmacologically acceptable sodium salt and an acne controlling compound selected from the group consisting of methyclothiazide, polythiazide and trichlormethazide, which is therapeutically effective in increasing sodium excretion in the sebaceous gland thereby controlling acne vulgaris eruptions. The conjoint use of the sodium salt and the acne controlling compound significantly reduces the unwanted side effects caused by the administration of the acne controlling compound including nausea, dizziness, hypotension and diuresis, which are experienced in some patients when the acne controlling compound is employed in acne treatment absent the conjoint use of the sodium salt.
Patent number: 4443442
Filing date: Dec 21, 1979
Issue date: Apr 17, 1984
Inventor: Scott D. Skillern



What is claimed is:

1. A method for the treatment of acne vulgaris in a human having acne vulgaris which comprises conjointly administering an acne controlling compound induced side effect reducing amount comprising at least 0.2 grams of sodium in a form of a pharmacologically acceptable sodium salt and a therapeutically effective amount of an acne controlling compound selected from the group consisting of polythiazide and trichlormethiazide.

2. A method for the treatment of acne vulgaris in a human having acne vulgaris which comprises conjointly administering on a bi-daily basis an acne controlling compound induced side effect reducing amount comprising at least 0.2 grams of sodium in the form of a pharmacologically acceptable sodium salt and a therapeutically effective amount of an acne controlling compound selected from the group consisting of polythiazide and trichlormethiazide.

3. A pharmacological dose unit which is useful in the treatment of acne vulgaris in a human having acne vulgaris comprising in combination 0.2 grams to 0.8 grams of sodium in the form of a pharmacologically acceptable sodium salt and a therapeutically effective amount of an acne controlling compound selected from the group consisting of polythiazide and trichlormethiazide.

4. A pharmacological dose unit, as defined in claim 3, wherein the acne controlling compound is polythiazide in an amount of 0.5 to 5.0 mg.

5. A pharmacological dose unit, as defined in claim 3, wherein the acne controlling compound is trichlormethiazide in an amount from 0.5 to 5.0 mg.