Stanley Erck, Novavax CEO (Andrew Harnik, AP Images)

Af­ter sput­ter­ing on the launch pad, No­vavax fi­nal­ly gets its EUA ap­pli­ca­tion in. Does it mat­ter?

No­vavax has fi­nal­ly met one of its self-im­posed dead­lines for the long-await­ed EUA fil­ing for its Covid-19 vac­cine.

Af­ter re­peat­ed­ly dis­ap­point­ing in­vestors while rais­ing ques­tions about its abil­i­ty to man­u­fac­ture the vac­cine to FDA stan­dards, No­vavax an­nounced late Mon­day that the EUA has fi­nal­ly been dis­patched to the agency.

For No­vavax, the pan­dem­ic has been a god­send, of­fer­ing the biotech a shot at its first ap­proval — and this for what has been an enor­mous new mar­ket. But while No­vavax floun­dered re­peat­ed­ly at the FDA, Pfiz­er/BioN­Tech and Mod­er­na — which yes­ter­day fol­lowed up with their for­mal ap­proval — cruised ahead with 2 new mR­NA vac­cines that have dom­i­nat­ed the US mar­ket, with J&J’s one shot jab in the mix.

Endpoints News

Unlock this article instantly by becoming a free subscriber.

You’ll get access to free articles each month, plus you can customize what newsletters get delivered to your inbox each week, including breaking news.