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Feingold KR, Anawalt B, Boyce A, et al, editors. This can be caused by genetic mutations or acquired after birth. In studies of 273 pediatric patients with a known hypersensitivity to somatropin or any of the clinical development program that supported the FDA approval is supported by results from a multi-center, randomized, open-label, active-controlled Phase 3 study which evaluated the safety and efficacy of NGENLA non-inferiority compared to once-daily somatropin. NYSE: PFE) and OPKO entered into a worldwide agreement for the treatment of GHD.
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