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BioWorld - Tuesday, January 13, 2026
Home » Topics » Drugs » Vaccine

Vaccine
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Fosun Pharma acquires vaccine firm Antejin in deal worth up to $626M

Nov. 2, 2021
By Doris Yu
Fosun Pharmaceutical Group Co. Ltd. has acquired a 73% stake of Antejin Biotech Co. Ltd. in a merger and acquisition deal worth up to ¥4.006 billion (US$626.2 million) to expand its pipeline in the field of bacterial vaccines. To kick off, Shanghai-based Fosun purchased about 32.52% equity interest in Antejin from nine shareholders for about ¥1.108 billion in cash.
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CDC advisory committee recommends Pfizer-Biontech COVID-19 vaccine for children

Nov. 2, 2021
By Lee Landenberger
In a move that had been expected, the CDC’s Advisory Committee on Immunization Practices unanimously recommended the Pfizer Inc.-Biontech SE COVID-19 vaccine as safe and beneficial for children ages 5 through 11. The recommendation, coming from a 14-0 vote, is the committee’s way of reassuring the American public that the vaccine is safe, according to committee member Beth Bell, clinical professor in the School of Public Health at the University of Washington in Seattle.
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Coronavirus vaccine/therapeutics illustration

The battle against COVID-19 rages on amid development hits and misses

Nov. 2, 2021
By Karen Carey
As booster shots become increasingly available and COVID-19 vaccines for young children are introduced into pediatric offices, several potential therapeutics to battle the SARS-CoV-2 virus are lining up for regulatory authorizations.
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Myocarditis concerns derail hopes of speedy EUA for Moderna COVID-19 vaccine in children

Nov. 1, 2021
By Michael Fitzhugh
An ongoing evaluation of heart muscle inflammation risk, a key concern with mRNA COVID-19 vaccines globally, could delay through January 2022 completion of an FDA review of Moderna Inc.'s vaccine in adolescents 12 to 17 years of age. The side effect, called myocarditis, has been a particular concern with regulators, especially for adolescents and young men.
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FDA awards EUA to Pfizer’s COVID-19 vaccine for children

Oct. 29, 2021
By Lee Landenberger
The FDA has granted emergency use authorization (EUA) to the COVID-19 vaccine created by Pfizer Inc.-Biontech SE for use in children ages 5 through 11. This is the first EUA for a COVID-19 vaccine to be awarded for this group of roughly 28 million children in the U.S. and it comes after weeks of lengthy debate among experts about the wisdom of targeting the young demographic.
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Bioplus Interphex Korea 2021: Plant-based vaccines, therapeutics could be way forward for COVID-19, future pandemics

Oct. 28, 2021
By Gina Lee
Plants could be an alternative vaccine platform for both COVID-19 and future pandemics, shaking up a biologics sector that is currently mostly protein-based. South Korean company Bioapplications Inc., for example, is aiming to have a plant-derived booster shot for COVID-19 in the clinic in 2022.
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Fosun Pharma acquires vaccine firm Antejin in deal worth up to $626M

Oct. 28, 2021
By Doris Yu
Fosun Pharmaceutical Group Co. Ltd. has acquired a 73% stake of Antejin Biotech Co. Ltd. in a merger and acquisition deal worth up to ¥4.006 billion (US$626.2 million) to expand its pipeline in the field of bacterial vaccines. To kick off, Shanghai-based Fosun purchased about 32.52% equity interest in Antejin from nine shareholders for about ¥1.108 billion in cash.
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Japanese companies make headway in domestic vaccine R&D

Oct. 26, 2021
By David Ho and Gina Lee
The race for a Japan-made COVID-19 vaccine is heating up as players make progress with their trials. Daiichi Sankyo Co. Ltd. recently shared the results from its phase I/II trial for DS-5670, its mRNA vaccine. The mRNA vaccine candidate initiated studies in March 2021. The findings showed that in terms of immunogenicity, both neutralizing activity and IgG titer increased after the vaccination.
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Child vaccine

VRBPAC says yes to pediatric vaccine, cautions against mandates

Oct. 26, 2021
By Mari Serebrov
The FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted 17-0, with one abstention, that the benefits of Pfizer Inc.-Biontech SE pediatric formulation of its two-dose COVID-19 vaccine outweigh its risks for children ages 5 through 11. Many of those votes came with caveats, as the VRBPAC members struggled with the unknowns of the vaccine and the fear that schools would mandate its use, even though it would still be considered experimental if the FDA grants it an emergency use authorization.
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Brain scan illustration

Greater risk for neurological complications from COVID-19 infection vs. vaccination, analysis shows

Oct. 25, 2021
By Nuala Moran
LONDON – A U.K. study following up 32.5 million people for 28 days after their first dose of a COVID-19 vaccine has shown an increased risk of hemorrhagic stroke after receiving the Pfizer Inc./Biontech SE product, and confirmed case reports of an increased risk of developing Guillain-Barré syndrome after the Astrazeneca plc vaccine.
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