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Moderna, Inc.: Moderna Receives FDA Emergency Use Authorization for Omicron-Targeting Bivalent COVID-19 Booster Vaccine in Children 6 Months Through 5 Years of Age

MRNA-1273.222 Targets the BA.4/BA.5 Strains of Omicron VariantAuthorization Is Based Upon Clinical and Pre-Clinical Data for Moderna's Bivalent VaccinesCAMBRIDGE, MA / ACCESSWIRE / December 8, 2022 / Moderna
United Kingdom Lavina Talukdar Chris Ridley Exchange Commission Moderna Inc View Corporate Communications

Clovis Oncology Presents Data from TRITON3 Phase 3 Trial of Rubraca® (rucaparib) at the 29th Annual Prostate Cancer Foundation Scientific Retreat

Clovis Oncology, Inc. today announced the presentation of data from the TRITON3 Phase 3 trial in men with metastatic castration-resistant prostate cancer with BRCA or ATM mutations. The presentation... | October 27, 2022
United States Alanh Bryce Patrickj Mahaffy Clovis Oncology Inc National Cancer Institute Exchange Commission

First time in Slovenia: meeting of the HERCA WGE

On 19 and 20 October 2022, Slovenian Nuclear Safety Administration hosted the 24th meeting of the Working Group on Emergencies (WGE) established by the Heads of European Radiological Protection Competent Authorities (HERCA).
European Nuclear Regulator Association European Commission International Atomic Energy Agency Emergency Response Centre National Emergency Response Plan World Health Organisation
Source: gov.si

Moderna, Inc.: 90-Day Analysis Shows Moderna's Omicron BA.1-Targeting Bivalent Vaccine, mRNA-1273.214, Demonstrates Superior Antibody Response as Fourth Booster Compared to Spikevax Prototype Booster

Data indicate durable immune response from bivalent booster after three months of follow-upmRNA-1273.214 also demonstrated potent response to Omicron BA.2.75CAMBRIDGE, MA / ACCESSWIRE / October 19, 2022
United Kingdom Elise Meyer Lavina Talukdar Exchange Commission Corporate Communications Moderna Inc

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Investegate |BioNTech SE Announcements | BioNTech SE: Pfizer and BioNTech Submit Application to U.S. FDA for Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent Vaccine Booster in Children 5 Through 11 Years of Age

Investegate announcements from BioNTech SE, Pfizer and BioNTech Submit Application to U.S. FDA for Emergency Use Authorization of Omicron BA.4/BA.5-Adapted Bivalent Vaccine Booster in Children 5 Through 11 Years of Age
United States United Kingdom Sylke Maas Fosun Pharma Centers For Disease Drug Administration

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