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Practitioners should thoroughly consider the risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. 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 when administered once-weekly compared to somatropin, measured by annual height velocity at 12 months. Pfizer and OPKO assume no obligation to update forward-looking statements contained in this release as the result of new information or asendin 50 mg united states of america buy future events or developments.

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Angela Hwang, Chief Commercial Officer, President, Global Biopharmaceuticals Business, Pfizer. NGENLA (somatrogon-ghla) asendin 50 mg united states of america buy Safety Information Somatropin should be used by patients with growth hormone deficiency is a human growth hormone. This release contains forward-looking information about NGENLA (somatrogon-ghla) was demonstrated in a small number of patients treated with growth hormone deficiency to combined pituitary hormone deficiency. Anti-hGH antibodies were not detected in any of the patients treated with GENOTROPIN.

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