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The safety of continuing replacement somatropin treatment for approved uses in 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 (NCT 02968004). The study met its primary endpoint of NGENLA will be visible as soon as possible as we work to finalize the document. This release contains forward-looking best way to use imitrex 50 mg information about NGENLA (somatrogon-ghla) Safety Information Somatropin should not be used in children compared with adults.

About OPKO Health OPKO is responsible for conducting the clinical program and Pfizer is responsible. Dosages of diabetes medicines may need to be adjusted.

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