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InflaRx Announces First Patient Dosed in Phase III Trial with Vilobelimab in Pyoderma Gangrenosum

InflaRx Announces First Patient Dosed in Phase III Trial with Vilobelimab in Pyoderma Gangrenosum
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InflaRx: EMA Reviews MAA For Vilobelimab For Critically Ill COVID-19 Patients; Stock Up In Premarket

InflaRx N.V. (IFRX), a biotechnology company pioneering anti-inflammatory therapeutics targeting the complement system, Wednesday said the European Medicines Agency or EMA has validated its Marketing Authorization Application or MAA for Vilobelimab to treat Critically Ill COVID-19 Patients. ....

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InflaRx Shares Soar 40% on FDA Emergency Use Authorization of Gohibic for Covid-19

By Denny Jacob

InflaRx NV shares were on pace Wednesday for its best three-day stretch on record, a day after Gohibic, a monoclonal anti-human complement factor C5a antibody it is developing,. | April 5, 2023 ....

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FDA Grants Emergency Use Authorization for InflaRx COVID-19 Drug in Critically Ill Patients

Biopharmaceutical company InflaRx NV's monoclonal antibody has been granted emergency use authorization (EUA) by the Food and Drug Administration (FDA) for the treatment of COVID-19 . ....

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InflaRx's Gohibic Gets Emergency Use Authorization from FDA for Covid-19 Hospitalized Patients

By Denny Jacob

InflaRx NV on Tuesday said Gohibic, a monoclonal anti-human complement factor C5a antibody, was granted emergency use authorization by the Food and Drug Administration.

The. | April 4, 2023 ....

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