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Meanwhile, 30% of functional dyspepsia patients have slow gastric emptying [5]

The reference product exclusivity period under the BPCIA means no biosimilar can rely on the FDAs pembrolizumab safety data until 12 years after first approval which for pembrolizumab (approved September 2014) is September 2026

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These mistakes account for most reconstitution failures and the disappointing results that follow

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Annals of Translational Medicine , 11(2), pp.132132