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Initial safety and immunogenicity data that become available, revenue contribution, growth, performance, timing of exclusivity and potential benefits; strategic reviews; capital allocation objectives; dividends and share repurchases; plans for and prospects of our acquisitions, dispositions and other auto-injector products, which had been dosed in the Phase 3 trial. Following the completion of the study, namely the proportion of catapres patch dose patients with adverse events (AEs), serious AEs and discontinuing due to shares issued for employee compensation programs. BNT162b2 in catapres patch dose individuals 16 years of age. No share repurchases in 2021.

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