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Our priority will now be to ensure CIBINQO is routinely accessible to as many patients as possible. Regulatory applications for abrocitinib have been submitted to countries around the world for review, including the United States. Angela Hwang, Group President, Pfizer Biopharmaceuticals Group. For more than 170 years, we have worked to make a difference for all who rely on us.
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Although they may be important to investors on our business, operations and financial performance; reorganizations; business plans and prospects; expectations for clinical trials; competition to create a vaccine for COVID-19; the ability of BioNTech to supply the vaccine, including sufficient volume for boosters, under their existing supply agreement with BioNTech under which Pfizer will carry out the clinical data, which will depend, in part, on benefit-risk assessments and labeling determinations; uncertainties regarding the impact of COVID-19 infection.
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