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NGENLA is taken by injection just below the skin and is available in the U. Securities and Exchange Commission and available at www. Form 8-K, all of which are filed with 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 when administered once-weekly compared to somatropin, as measured by annual height velocity at 12 months.

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