OR10-05 Phase 3 FliGHt Trial: Experience of Switching from Daily Growth Hormone Therapy to Once-Weekly TransCon HGH in Children with Growth Hormone Deficiency

التفاصيل البيبلوغرافية
العنوان: OR10-05 Phase 3 FliGHt Trial: Experience of Switching from Daily Growth Hormone Therapy to Once-Weekly TransCon HGH in Children with Growth Hormone Deficiency
المؤلفون: Aristides K Maniatis, Gail J. Mick, Aimee D Shu, David B Karpf, Wenjie Song, Mary Jennifer Abuzzahab, Larry Deeb, Larry A. Fox, Paul S. Thornton, Paul Saenger, Jessica M Peng, Katie A. Woods, Kent Reifschneider, Ulhas M Nadgir, Samuel J Casella
المصدر: Journal of the Endocrine Society
بيانات النشر: The Endocrine Society, 2020.
سنة النشر: 2020
مصطلحات موضوعية: medicine.medical_specialty, business.industry, Endocrinology, Diabetes and Metabolism, Understanding and Treating Pediatric Growth Disorders, Once weekly, Growth hormone, medicine.disease, Growth hormone deficiency, Endocrinology, Pediatric Endocrinology, Internal medicine, Medicine, business, hormones, hormone substitutes, and hormone antagonists, AcademicSubjects/MED00250
الوصف: Background: The Phase 3 fliGHt Trial evaluated children with growth hormone deficiency (GHD) of a broad range of baseline demographics and treatment durations who switched from daily growth hormone (hGH; somatropin) therapy to once-weekly TransCon hGH. TransCon hGH is an investigational long-acting prodrug consisting of 3 components: hGH, an inert carrier that protects it, and a linker that temporarily binds the two. When injected into the body, at physiologic pH and temperature, unmodified hGH is gradually released in a predictable manner. Methods: All subjects initiated open-label once-weekly TransCon hGH 0.24 mg hGH/kg/week irrespective of prior daily hGH dose. Subjects 3 to 17 years old must have been treated with daily hGH for 13 to 130 weeks; subjects 6 months to 3 years old may have been treatment-naïve or treated with daily hGH for ≤130 weeks. The primary objective was to assess safety and tolerability over this 26-week trial. Efficacy measures included annualized height velocity (AHV), height standard deviation score (SDS), and insulin-like growth factor 1 (IGF-1) SDS. Results: Of the 146 enrolled subjects, 98.6% completed the trial. Mean age at baseline was 10.6 years (range: 1, 17). The majority (97.9%) were treatment-experienced with a prior daily hGH mean dose of 0.29 mg/kg/week (range: 0.13, 0.49); 3 subjects were treatment-naïve and Conclusions: TransCon hGH treatment outcomes, including AHV and height SDS, were as expected across a diversity of ages, disease characteristics, and treatment experiences, reflective of a real-world setting. Dose titrations of TransCon hGH demonstrated a predictable IGF-1 response. Switching to TransCon hGH resulted in a similar adverse event profile to daily hGH therapy.
تدمد: 2472-1972
DOI: 10.1210/jendso/bvaa046.963
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18cef01ed6feced761a45558d43332c6
https://doi.org/10.1210/jendso/bvaa046.963
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....18cef01ed6feced761a45558d43332c6
قاعدة البيانات: OpenAIRE
الوصف
تدمد:24721972
DOI:10.1210/jendso/bvaa046.963