Drug intelligence / Profile preview

etretinate + triamcinolone acetonide

Development stage
Preclinical
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules
Administration
Oral (etretinate), Topical Or Intralesional Injection Possible For Triamcinolone Acetonide; Route Depends On Formulation Specifics Which Are Not Detailed In Available Sources.
01

Overview

This is a combination drug consisting of etretinate and triamcinolone acetonide. **Etretinate** is a second-generation synthetic aromatic retinoid used primarily for the treatment of severe psoriasis and other keratinization disorders. Its mechanism involves binding to retinoic acid receptors (RARs), acting as an agonist to modulate gene expression involved in cell differentiation and proliferation, particularly affecting keratinocytes[2][3][6]. Etretinate was withdrawn from several markets due to its long half-life and risk of teratogenicity but remains notable for its efficacy in dermatological conditions[2][6]. **Triamcinolone acetonide** is a synthetic corticosteroid with anti-inflammatory, immunosuppressive, and antipruritic properties. It acts by binding to glucocorticoid receptors, inhibiting inflammatory mediators and suppressing immune responses.

Other names
etretinate + triamcinolone acetonideRo 10-9359 + triamcinolone acetonide
02

Targets

RARA (Retinoic acid receptor alpha)GR (Glucocorticoid receptor)

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