Method for the use of orally administered 13-cis-retinoic acid i

Drug – bio-affecting and body treating compositions – Antigen – epitope – or other immunospecific immunoeffector – Recombinant or stably-transformed bacterium encoding one or...

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424344, A61K 3120

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043224385

ABSTRACT:
In a method of alleviating nodulocystic and conglobate acne in humans by the oral administration of 13-cis-retinoic acid, the improvement comprising: administering the 13-cis-retinoic acid in a high dosage of from 1.0 to 2.0 mg/kg/day for from 2 to 4 weeks; and reducing the amount of 13-cis-retinoic acid to a low dosage of from 0.25 to 0.5 mg/kg/day for a period of from 12 to 14 weeks, so that the total treatment period is about 16 weeks.

REFERENCES:
Strauss et al., J. Invest. Dermatol., 70:228; 4-1978.
Gunby-J.A.M.A., 240:7,610, 8/18/78.
Investigative Drug Brochure, Ro-4-3780, (Hoffman LaRoche, Inc.), 2-1978.
New England Journal of Medicine, vol. 300, No. 7, pp. 329-333 & 359-360, (2-1979).
J.A.M.A., vol. 240, No. 7, p. 610, (8-1978).
Demratologica, 157 (Suppl. 1): 11-12, (1978).
Ophthalmology 85:35, (7-1978).

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