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BioNTech Announces First Quarter 2021 Financial Results and Corporate Update


Press release content from Globe Newswire. The AP news staff was not involved in its creation.
BioNTech Announces First Quarter 2021 Financial Results and Corporate Update
BioNTech SEMay 10, 2021 GMT
More than 450 million doses of BNT162b2 supplied to 91 countries or territories worldwide as of May 6, 2021
Signed agreements for over 1.8 billion doses of BNT162b2 in 2021 and first contracts signed for periods 2022 and beyond
Announced planned expansion of global footprint to Asia with establishment of first regional headquarters for south east Asia in Singapore, including a fully-integrated and state-of-the art mRNA manufacturing facility
In oncology, a first-in-human Phase 1 trial started for the neoantigen-targeting T cell therapy, BNT221. The development of BioNTech’s oncology pipeline has continued to accelerate with 14 product candidates now in 15 ongoing trials ....

United States , United Kingdom , South Africa , Sylke Maas , Sanofi Libtayo , Ugur Sahin , Fosun Pharma , Autogene Cevumeran , Us Centers For Disease , Singaporean Economic Development Board , Association For Cancer Immunotherapy , European Commission , Drug Administration , International Olympic Committee , Bayer Animal Health , Development Expenses , European Union , European Medicines Agency , Roche Group , Health Canada , Full Year , Corporate Update , Annual Report , Disease Control , New England Journal , Use Authorization ,

BioNTech SE: BioNTech Announces First Quarter 2021 Financial Results and Corporate Update


BioNTech SE: BioNTech Announces First Quarter 2021 Financial Results and Corporate Update
More than 450 million doses of BNT162b2 supplied to 91 countries or territories worldwide as of May 6, 2021
Signed agreements for over 1.8 billion doses of BNT162b2 in 2021 and first contracts signed for periods 2022 and beyond
Announced planned expansion of global footprint to Asia with establishment of first regional headquarters for south east Asia in Singapore, including a fully-integrated and state-of-the art mRNA manufacturing facility
In oncology, a first-in-human Phase 1 trial started for the neoantigen-targeting T cell therapy, BNT221. The development of BioNTech s oncology pipeline has continued to accelerate with 14 product candidates now in 15 ongoing trials ....

United States , United Kingdom , South Africa , Sanofi Libtayo , Sylke Maas , Ugur Sahin , Fosun Pharma , Autogene Cevumeran , Us Centers For Disease , Singaporean Economic Development Board , International Olympic Committee , Bayer Animal Health , Development Expenses , European Union , Global External Communications , Association For Cancer Immunotherapy , Drug Administration , European Commission , European Medicines Agency , Roche Group , Health Canada , Full Year , Corporate Update , Annual Report , Disease Control , New England Journal ,

Pfizer Inc.: Pfizer and BioNTech Confirm High Efficacy and No Serious Safety Concerns Through Up to Six Months Following Second Dose in Updated Topline Analysis of Landmark COVID-19 Vaccine Study


(0)
Analysis of 927 confirmed symptomatic cases of COVID-19 demonstrates BNT162b2 is highly effective with 91.3% vaccine efficacy observed against COVID-19, measured seven days through up to six months after the second dose
Vaccine was 100% effective in preventing severe disease as defined by the U.S. Centers for Disease Control and Prevention and 95.3% effective in preventing severe disease as defined by the U.S. Food and Drug Administration
Vaccine was 100% effective in preventing COVID-19 cases in South Africa, where the B.1.351 lineage is prevalent
Vaccine safety now evaluated in more than 44,000 participants 16 years of age and older, with more than 12,000 vaccinated participants having at least six months follow-up after their second dose ....

South Africa , United States , United Kingdom , Sylke Maas , Albert Bourla , Chuck Triano , Ugur Sahin , Fosun Pharma , Jerica Pitts , Centers For Disease , Us Centers For Disease , Drug Administration , Bayer Animal Health , Exchange Commission , Pfizer Inc , European Union , Roche Group , Vaccine Administration Under Emergency Use Authorization , Disease Control , Biologics License Application , Chief Executive Officer , Emergency Use Authorization , Coronavirus Disease , Fact Sheet , Healthcare Providers Administering Vaccine , Vaccination Providers ,

BioNTech SE: Pfizer and BioNTech Confirm High Efficacy and No Serious Safety Concerns Through Up to Six Months Following Second Dose in Updated Topline Analysis of Landmark COVID-19 Vaccine Study


(1)
Analysis of 927 confirmed symptomatic cases of COVID-19 demonstrates BNT162b2 is highly effective with 91.3% vaccine efficacy observed against COVID-19, measured seven days through up to six months after the second dose
Vaccine was 100% effective in preventing severe disease as defined by the U.S. Centers for Disease Control and Prevention and 95.3% effective in preventing severe disease as defined by the U.S. Food and Drug Administration
Vaccine was 100% effective in preventing COVID-19 cases in South Africa, where the B.1.351 lineage is prevalent
Vaccine safety now evaluated in more than 44,000 participants 16 years of age and older, with more than 12,000 vaccinated participants having at least six months follow-up after their second dose ....

South Africa , New York , United States , United Kingdom , Sylke Maas , Albert Bourla , Chuck Triano , Ugur Sahin , Fosun Pharma , Jerica Pitts , Centers For Disease , Us Centers For Disease , Pfizer Inc Nasdaq , Drug Administration , Bayer Animal Health , Exchange Commission , European Union , Roche Group , Vaccine Administration Under Emergency Use Authorization , Disease Control , Biologics License Application , Chief Executive Officer , Marketing Authorizations Holder , Emergency Use Authorization , Adverse Events , Fact Sheet ,