Drug intelligence / Profile preview

cenacitinib adipate

Development stage
Discontinued
Lead developer
Ventyx Biosciences
Modality
Small Molecules
Administration
Oral
01

Overview

Cenacitinib adipate (VTX-958 adipate) is an orally bioavailable, highly selective, and potent allosteric inhibitor of tyrosine kinase 2 (TYK2). Developed by Ventyx Biosciences (which was acquired by Eli Lilly in 2026), it targets the pseudokinase (JH2) domain of TYK2 to selectively inhibit downstream signaling of cytokines such as IL-12, IL-23, and Type I interferons, which are key drivers of chronic inflammation. The adipate salt formulation was specifically evaluated in a Phase 1 study comparing modified-release tablet prototypes against standard film-coated tablets to optimize pharmacokinetics, safety, and tolerability. Although cenacitinib was advanced into Phase 2 clinical trials for moderate-to-severe plaque psoriasis, psoriatic arthritis, and Crohn's disease, development was terminated across these indications due to insufficient efficacy compared to internal targets and competitors.

Other names
cenacitinib
02

Targets

JAK1 JH2 (JAK1 pseudokinase domain)TYK2 (Tyrosine kinase 2)

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