Pharmaceutical giant Pfizer Inc (NYSE:PFE) and immunotherapy company BioNTech SE (Nasdaq:BNTX) announced on Friday that they have won a contract from the Japanese Government to supply 120 million doses of their BNT162 mRNA-based vaccine candidate against SARS-CoV-2, the virus that causes COVID-19.
Financial details of the agreement with the Ministry of Health, Labour and Welfare were not disclosed.
BNT162 is based on BioNTech's proprietary mRNA technology and supported by Pfizer's global vaccine development and manufacturing capabilities. The vaccine development programme is evaluating at least four experimental vaccine candidates, each of which represents a unique combination of messenger RNA (mRNA) format and target antigen.
The BNT162 vaccine candidates are currently in clinical studies and are not yet approved for distribution anywhere in the world. Two of the four investigational vaccine candidates, BNT162b1 and BNT162b2, recently received Fast Track designation from the US Food and Drug Administration (FDA).
Deliveries of the vaccine candidate to Japan are planned for the first half of 2021, subject to regulatory approval.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval