- COVID-19 vaccine Phase 2/3 study in children 6 months to under 6 years has successfully met its primary endpoint with robust neutralizing antibody titers similar to adults. Moderna is moving forward with global regulatory submissions for mRNA-1273 for primary vaccination of children 6 months to under 6 years of age.
- Moderna has initiated a submission to the FDA for emergency use authorization of mRNA-1273 in children 6 to under 12 years of age; mRNA-1273 is approved for use in this age group in Europe, Canada, and Australia.
- In an interim analysis of a Phase 2 study of influenza vaccine candidate mRNA-1010, no significant safety concerns were identified, and the immunogenicity data is consistent with a potential for superiority to standard dose vaccine for influenza A strains.
- Moderna is advancing vaccine candidates against five viruses that cause latent infections, three of which are in clinical trials. In a Phase 2 study, the CMV vaccine (mRNA-1647) was observed to be generally well tolerated and interim data demonstrates strong immunogenicity.
- Moderna announces an increase in signed Advance Purchase Agreements for 2022 from $19 billion announced on February 24, 2022, to $21 billion.
Morgan Stanley Maintains Equal-Weight on Nutanix, Raises Price Target to $24
Morgan Stanley analyst Meta Marshall maintains Nutanix (NASDAQ:NTNX) with a Equal-Weight and raises the price target from $22 to $24.
