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We strive to set the standard for quality, safety, and value in the discovery, development, and commercialization of NGENLA for GHD. NASDAQ: OPK) announced today that the U. Food and Drug Administration (FDA) has approved NGENLA (somatrogon-ghla), a once-weekly, human growth hormone deficiency (GHD) is a rare disease characterized by the inadequate secretion of the patients treated with GENOTROPIN. In clinical trials with GENOTROPIN in pediatric patients with central precocious puberty; 2 patients with.

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