Journal
JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
Volume 36, Issue 3, Pages 261-269Publisher
WALTER DE GRUYTER GMBH
DOI: 10.1515/jpem-2022-0359
Keywords
children; Genotropin; growth hormone; growth hormone deficiency; height velocity; IGF-1; long-acting growth hormone; pediatric; somatrogon; somatropin
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This study evaluated the safety and efficacy of once-weekly somatrogon as a treatment for children with growth hormone deficiency. The results showed that once-weekly somatrogon had a sustained improvement in height for children with growth hormone deficiency.
Objectives: Somatrogon is a long-acting recombinant human growth hormone (GH) employed as a once-weekly treatment for children with GH deficiency (GHD). A 12-month, phase 2 study of once-weekly somatrogon vs. once-daily GH (Genotropin (R)) was initiated, after which participants could enroll into an open-label extension (OLE) evaluating the safety and efficacy of long-term somatrogon treatment.Methods: There were five study periods, Periods I and II were 6 months each while Periods III, IV, and V were 12 months each. In the main study (Periods I and II), 53 prepubertal children with GHD were randomized to once weekly somatrogon (0.25, 0.48, or 0.66 mg/kg/week) or once daily Genotropin (0.034 mg/kg/day); 48 continued into the OLE, consisting of Period III (original somatrogon dose; Genotropin recipients randomized to one of three somatrogon doses), Period IV (somatrogon 0.66 mg/kg/week), and Period V (prefilled somatrogon pen [0.66 mg/kg/week]).Results: At the end of Period III, the mean +/- SD annual height velocity (HV) for 0.25, 0.48, and 0.66 mg/kg/week somatrogon groups was 7.73 +/- 1.89, 7.54 +/- 1.28, and 8.81 +/- 1.12 cm/year, respectively; HV was sustained during Periods IV/V. Height SD scores (SDS) showed progressive improvement throughout the OLE, regardless of initial cohort assignment, approaching the normal range (-0.69 +/- SD 0.87) at the end of Period V Year 1. Mild or moderate treatment emergent adverse events were reported in 81.3% of participants, most unrelated to study drug.Conclusions: Up to 5 years of once-weekly somatrogon was well tolerated and resulted in sustained improvement in height SDS and delta height SDS in prepubertal short children with GHD. Clinicaltrials.gov:NCT01592500.
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