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Ren et al

The approval was backed by the Phase II open-label AGAVE-201 trial, where treatment with a 0.3-mg/kg dose of Niktimvo elicited an overall response rate of 75%, with a median time to response of 1.5 months

Constantinescu, C

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Date of Mfg ( Scrub)

This prospective, phase IV study used an integrated genomic analysis to identify markers associated with 1-month change in IGF-I (IGF-I) following initiation of recombinant human (r-h)GH therapy in treatment-nave children with GH deficiency (GHD) ( n =166) or Turner syndrome (TS) ( n =147)