InflaRx gains FDA EUA for Gohibic in COVID-19 patients
The US Food and Drug Administration (FDA) has issued an emergency use authorization (EUA) for the use of Germany-headquartered clinical-stage biotech InflaRx’ (Nasdaq: IFRX) Gohibic (vilobelimab) injection.
The drug is indicated for the treatment of COVID-19 in hospitalized adults when initiated within 48 hours of receiving invasive mechanical ventilation or extracorporeal membrane oxygenation (artificial life support).
News of the approval sent InflaRx’ shares up a massive 84% on Tuesday, and a further 14% to $4.30 in pre-market trading today.
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