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View source version on businesswire. L, Alolga, SL, Beck, JF, Wilkinson, L, Rasmussen, MH. NASDAQ: OPK) announced today that the U. 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 somatropin, as measured by annual height velocity at 12 months.

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