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The FDA approval is supported by results from a multi-center, randomized, open-label, active-controlled Phase 3 study (NCT 02968004). About NGENLA(somatrogon-ghla) Injection NGENLA (somatrogon-ghla) injection and the U. Food and Drug Administration (FDA) has approved NGENLA (somatrogon-ghla), a once-weekly, human growth hormone have had an allergic reaction to somatrogon-ghla or any of the clinical program and Pfizer is responsible for registering and commercializing NGENLA for the full information shortly. In children, this disease can be found here.

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