Etretinate


Etretinate is a medication developed by Hoffmann–La Roche that was approved by the FDA in 1986 to treat severe psoriasis. It is a second-generation retinoid. It was subsequently removed from the Canadian market in 1996 and the United States market in 1998 due to the high risk of birth defects. It remains on the market in Japan as Tigason.

Pharmacology

Etretinate is a highly lipophilic, aromatic retinoid. It is stored and released from adipose tissue, so its effects can continue long after dosage stops. It is detectable in the plasma for up to three years following therapy. Etretinate has a low therapeutic index and a long elimination half-life of 120 days, which make dosing difficult.
Etretinate has been replaced by acitretin, the free acid. While acitretin is less lipophilic and has a half-life of only 50 hours, it is partly metabolized to etretinate in the body, so that it is still a long-acting teratogen and pregnancy is prohibited for two years after therapy.

Precautions

Side effects are those typical of hypervitaminosis A, most commonly
Etretinate received FDA approval in 1986 for the treatment of severe psoriasis. However, it was voluntarily withdrawn from the Canadian market in 1996 and the United States market in 1998 due to its prolonged elimination half-life and significant teratogenic potential. Because the drug accumulates in adipose tissue, it can pose a high risk of birth defects for several years following the cessation of therapy. Etretinate was largely succeeded by its active metabolite, acitretin, which has a much shorter half-life and was approved by the FDA in 1996.
In Japan, the drug remains on market branded Tigason.