Drug intelligence / Profile preview

triamcinolone acetonide + tacrolimus

Development stage
Unknown
Lead developer
Shanghai Sixth People’s Hospital
Modality
Small Molecules
Administration
Topical
01

Overview

Triamcinolone acetonide + tacrolimus is a topical combination therapy primarily investigated and utilized for the treatment of vitiligo, particularly in stable or refractory cases. Triamcinolone acetonide is a synthetic glucocorticoid with potent anti-inflammatory and immunosuppressive properties; it acts as an agonist at the glucocorticoid receptor to suppress the production of inflammatory cytokines and modulate immune cell activity. Tacrolimus is a calcineurin inhibitor that binds to the intracellular protein FKBP12, forming a complex that inhibits the phosphatase activity of calcineurin. This inhibition prevents the dephosphorylation of the nuclear factor of activated T-cells (NFAT), thereby blocking T-cell activation and the subsequent autoimmune destruction of melanocytes. The combination is designed to provide synergistic efficacy in promoting repigmentation while potentially minimizing the side effects associated with long-term corticosteroid monotherapy. Research into this specific formulation has been notably conducted by institutions such as the Shanghai 6th People's Hospital.

Other names
triamcinolone acetonide and tacrolimus ointment
02

Targets

FKBP1AGR (Glucocorticoid receptor)CN (Calcineurin)

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