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Triamcinilone (kenalog)

Henry Ford Health System · FDA-approved active Small molecule

Triamcinolone is a synthetic corticosteroid that suppresses the immune system and reduces inflammation by binding to glucocorticoid receptors.

Triamcinolone is a synthetic corticosteroid that suppresses the immune system and reduces inflammation by binding to glucocorticoid receptors. Used for Rheumatoid arthritis and other inflammatory joint diseases, Allergic reactions and dermatitis, Asthma and respiratory inflammation.

At a glance

Generic nameTriamcinilone (kenalog)
SponsorHenry Ford Health System
Drug classCorticosteroid (glucocorticoid)
TargetGlucocorticoid receptor
ModalitySmall molecule
Therapeutic areaImmunology, Rheumatology, Dermatology, Endocrinology
PhaseFDA-approved

Mechanism of action

Triamcinolone acts as a glucocorticoid receptor agonist, entering cells and binding to intracellular glucocorticoid receptors. This leads to altered gene transcription, reducing production of pro-inflammatory cytokines and mediators. It suppresses T-cell activation, decreases antibody production, and stabilizes lysosomal membranes, resulting in broad anti-inflammatory and immunosuppressive effects.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results