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Moderna Announces its COVID-19 Vaccine Phase 2/3 Study in Children 6 Months to Under 6 Years Has Successfully Met Its Primary Endpoint

Moderna Announces its COVID-19 Vaccine Phase 2/3 Study in Children 6 Months to Under 6 Years Has Successfully Met Its Primary Endpoint
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Moderna Submits Amendment to the Emergency Use Authorization for an Additional Booster Dose of its COVID-19 Vaccine in the U S

Moderna Submits Amendment to the Emergency Use Authorization for an Additional Booster Dose of its COVID-19 Vaccine in the U S
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United statesUnited kingdomLavina talukdarColleen husseyExchange commissionUs centers for diseaseCorporate communicationsModerna incDrug administrationDisease controlBiologics license applicationVaccine adverse event reporting systemPrivate securities litigation reform actRisk factorAnnual reportVice president

Moderna Submits Amendment to the Emergency Use Authorization for an Additional Booster Dose of its COVID-19 Vaccine in the U S

Moderna Submits Amendment to the Emergency Use Authorization for an Additional Booster Dose of its COVID-19 Vaccine in the U S
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Moderna Submits Amendment to the Emergency Use Authorization for an Additional Booster Dose of its COVID-19 Vaccine in the U S

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United statesUnited kingdomLavina talukdarColleen husseyExchange commissionUs centers for diseaseCorporate communicationsModerna incDrug administrationDisease controlBiologics license applicationVaccine adverse event reporting systemPrivate securities litigation reform actAnnual reportVice presidentCoronavirus pandemic

Moderna, Inc : Moderna Submits Amendment to the Emergency Use Authorization for an Additional Booster Dose of its COVID-19 Vaccine in the U S

CAMBRIDGE, MA / ACCESSWIRE / March 17, 2022 / Moderna, Inc. (NASDAQ:MRNA), a biotechnology company pioneering messenger RNA (mRNA) therapeutics and vaccines, today announced that it has submitted a request

United statesUnited kingdomLavina talukdarColleen husseyExchange commissionUs centers for diseaseCorporate communicationsModerna incDrug administrationDisease controlBiologics license applicationVaccine adverse event reporting systemPrivate securities litigation reform actAnnual reportVice president