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The trial enrolled 76 children with severe IGFD and followed them for up to 8 years on twice-daily subcutaneous mecasermin administration, with growth velocity, height standard-deviation score, and adverse events as primary endpoints
Acta 1001 , 102106 (1989)
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These will involve tech transfer from known processes (reverse-engineering Lilly/Novo protocols) but navigating IP and regulatory barriers
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