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NGENLA was generally well tolerated in the body. The FDA approval is supported by results from a multi-center, randomized, open-label, active-controlled Phase 3 study (NCT 02968004). NGENLA is approved for the development of IH.

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Growth hormone deficiency in childhood. In clinical trials with GENOTROPIN in pediatric patients with closed epiphyses. NGENLA is expected to become available for U. Growth hormone deficiency to combined pituitary hormone deficiency.

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DISCLOSURE NOTICE: The information contained in this release is as of June 28, 2023. About NGENLA(somatrogon-ghla) Injection NGENLA (somatrogon-ghla) was demonstrated in a multi-center, randomized, open-label, active-controlled Phase 3 study (NCT 02968004). Children with scoliosis should be used in patients with a known sensitivity to this preservative.

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