Drug intelligence / Profile preview

auriclosene

Development stage
Phase 3
Lead developer
NovaBay Pharmaceuticals
Modality
Small Molecules
Administration
Topical, Ophthalmic, Otic, Intranasal, Intravesical
01

Overview

Auriclosene (NVC-422) is a synthetic, stable analog of N-chlorotaurine, a naturally occurring antimicrobial molecule produced by neutrophils during the oxidative burst. Developed by NovaBay Pharmaceuticals, it belongs to a class of compounds known as Aganocides. Auriclosene exerts broad-spectrum antimicrobial activity against bacteria (including multi-drug resistant strains), viruses, and fungi by inducing oxidative damage to essential microbial proteins and nucleic acids. Its mechanism involves the rapid transfer of chlorine to thiol and amino groups, leading to irreversible inactivation of microbial enzymes and structural proteins. Although it was investigated in Phase 2 clinical trials for indications such as adenoviral conjunctivitis, impetigo, and catheter-associated urinary tract infections, development was largely discontinued after failing to meet primary endpoints in late-stage trials.

Brand names
Aganocide
Other names
N,N-dichloro-2,2-dimethyltaurine
02

Targets

Neuraminidase

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