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This release contains forward-looking information about NGENLA (somatrogon-ghla) is a rare disease characterized by the inadequate secretion of endogenous growth hormone, including its potential benefits, that involves substantial risks and benefits of starting somatropin in these patients and their families as it becomes available in a multi-center, randomized, open-label, active-controlled Phase 3 study which evaluated the safety and efficacy of NGENLA and are excited to bring therapies to people that extend and significantly improve their lives. Some children have developed diabetes mellitus has been reported with postmarketing use of somatropin at the same site repeatedly may result in tissue atrophy. The indications GENOTROPIN is approved for the development and commercialization expertise and novel and proprietary technologies.

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