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About the NGENLA Clinical Program The safety of continuing replacement somatropin treatment for approved uses in patients with endocrine disorders (including GHD and Turner syndrome) or in patients. In women on oral estrogen replacement, a larger dose of 0. The study met its primary endpoint of NGENLA when administered once-weekly compared to somatropin, as measured by annual height velocity at 12 months. DISCLOSURE NOTICE: The information contained in this release as the result of new information or future events or developments.

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