Drug intelligence / Profile preview

PresSura

Development stage
Unknown
Lead developer
Eustralis Pharmaceuticals
Modality
Small Molecules
Administration
Intravenous, Oral
01

Overview

PresSura (also known as EU-C-001 or RO-0671721) is a selective, small-molecule neurokinin-1 (NK1) receptor antagonist originally developed by Roche and licensed to Eustralis Pharmaceuticals (trading as PresSura Neuro). The drug is designed to target neurogenic inflammation, restore blood-brain barrier integrity, and control elevated intracranial pressure (ICP) following traumatic brain injury (TBI). By blocking the binding of substance P to the NK1 receptor, PresSura prevents the vascular leakage and vasogenic edema that typically follow brain trauma. It is currently in Phase 2 clinical development for moderate-to-severe TBI and is also being explored for concussion-related conditions (such as post-concussion syndrome and chronic traumatic encephalopathy) and stroke.

Other names
N-(3,5-bis-trifluoromethylbenzyl)-N-methyl-6-(4-methyl-piperazin-1-yl)-4-o-tolyl-nicotinamide
02

Targets

TACR1 (Neurokinin‑1 Receptor)

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