Literature DB >> 23515245

Design of, and first data from, PATRO Children, a multicentre, noninterventional study of the long-term efficacy and safety of Omnitrope(®) in children requiring growth hormone treatment.

Roland Pfäffle1, Karl Otfried Schwab, Otilia Marginean, Mieczyslaw Walczak, Mieczyslaw Szalecki, Ellen Schuck, Markus Zabransky, Stefano Zucchini.   

Abstract

OBJECTIVE: To describe the rationale, design and first data from PATRO Children, a postmarketing surveillance of the long-term efficacy and safety of somatropin (Omnitrope(®)) for the treatment of children requiring growth hormone treatment.
METHODS: PATRO Children is a multicentre, open, longitudinal, noninterventional study being conducted in children's hospitals and specialised endocrinology clinics. The primary objective is to assess the long-term safety of Omnitrope(®) in routine clinical practice. Eligible patients are infants, children and adolescents (male or female) who are receiving treatment with Omnitrope(®) and who have provided informed consent. Patients who have been treated with another recombinant human growth hormone (rhGH) product before starting Omnitrope(®) are eligible for inclusion. All adverse events (AEs) are monitored and recorded, with particular emphasis on: long-term safety; the recording of malignancies; the occurrence and clinical impact of anti-hGH antibodies; the development of diabetes during Omnitrope(®) treatment in children short for gestational age (SGA); safety issues in patients with Prader-Willi syndrome (PWS). Efficacy assessments include auxological parameters, plus insulin-like growth factor-1 and insulin-like growth factor binding protein-3.
RESULTS: As of September 2012, 1837 patients were enrolled in the study from 184 sites in 10 European countries. To date, efficacy data are reassuring and consistent with previous studies. In addition, there have been no confirmed cases of diabetes occurring under Omnitrope(®) treatment, no reports of malignancy and no safety issues in PWS patients.
CONCLUSIONS: The efficacy and safety profile of Omnitrope(®) in the PATRO Children study so far are as expected. The ongoing study will extend the safety database for Omnitrope(®), and rhGH products more generally, in paediatric indications. Of particular interest, PATRO Children will add important information on the diabetogenic potential of rhGH in children born SGA, the risk of malignancies in children receiving rhGH, and AEs with a possible causal relationship to rhGH treatment in children with PWS.

Entities:  

Keywords:  Omnitrope®; children; paediatric; recombinant human growth hormone

Year:  2013        PMID: 23515245      PMCID: PMC3593298          DOI: 10.1177/2042018813479644

Source DB:  PubMed          Journal:  Ther Adv Endocrinol Metab        ISSN: 2042-0188            Impact factor:   3.565


  22 in total

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  12 in total

1.  A follow-up study to monitor adult height among Spanish children with growth hormone deficiency who received biosimilar human recombinant growth hormone (Omnitrope®) during a phase III clinical trial.

Authors:  Victoria Borrás Pérez; Juan Pedro López-Siguero; Gabriela Martínez; Raquel Corripio; Juan Manuel Fernández; Jose Ignacio Labarta; Marta Ferrer; Nuria Cabrinety; Pablo Prieto; Marta Ramón-Krauel; Jordi Bosch; Rafael Espino; Margarida Palla Garcia; Francisco Jose Rebollo
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2.  Long-term safety and efficacy of Omnitrope®, a somatropin biosimilar, in children requiring growth hormone treatment: Italian interim analysis of the PATRO Children study.

Authors:  Lorenzo Iughetti; Gianluca Tornese; Maria Elisabeth Street; Flavia Napoli; Claudia Giavoli; Franco Antoniazzi; Stefano Stagi; Caterina Luongo; Sara Azzolini; Letizia Ragusa; Gianni Bona; Clara Zecchino; Tommaso Aversa; Luca Persani; Laura Guazzarotti; Emiliano Zecchi; Alberto Pietropoli; Stefano Zucchini
Journal:  Ital J Pediatr       Date:  2016-11-03       Impact factor: 2.638

3.  Real-life GH dosing patterns in children with GHD, TS or born SGA: a report from the NordiNet® International Outcome Study.

Authors:  Oliver Blankenstein; Marta Snajderova; Jo Blair; Effie Pournara; Birgitte Tønnes Pedersen; Isabelle Oliver Petit
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Review 4.  Ten years of clinical experience with biosimilar human growth hormone: a review of safety data.

Authors:  Maria Victoria Borrás Pérez; Berit Kriström; Tomasz Romer; Mieczyslaw Walczak; Nadja Höbel; Markus Zabransky
Journal:  Drug Des Devel Ther       Date:  2017-05-16       Impact factor: 4.162

Review 5.  Ten years' clinical experience with biosimilar human growth hormone: a review of efficacy data.

Authors:  Juan Pedro López-Siguero; Roland Pfäffle; Philippe Chanson; Mieczyslaw Szalecki; Nadja Höbel; Markus Zabransky
Journal:  Drug Des Devel Ther       Date:  2017-05-16       Impact factor: 4.162

6.  Adherence and long-term growth outcomes: results from the easypod connect observational study (ECOS) in paediatric patients with growth disorders.

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8.  Acceptance of a reusable self-injection device for recombinant human growth hormone: final data from a questionnaire-based, cross-sectional, international, multicenter, observational study in pediatric patients.

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Journal:  Med Devices (Auckl)       Date:  2016-09-07

9.  Design of the long-term observational cohort study with recombinant human growth hormone in Korean children: LG Growth Study.

Authors:  Sochung Chung; Jae-Ho Yoo; Jin Ho Choi; Young-Jun Rhie; Hyun-Wook Chae; Jae Hyun Kim; Il Tae Hwang; Choong Ho Shin; Eun Young Kim; Kee-Hyoung Lee
Journal:  Ann Pediatr Endocrinol Metab       Date:  2018-03-22

10.  Safety and Effectiveness of Recombinant Human Growth Hormone in Children with Turner Syndrome: Data from the PATRO Children Study.

Authors:  Philippe Backeljauw; Shankar Kanumakala; Sandro Loche; Karl Otfried Schwab; Roland Werner Pfäffle; Charlotte Höybye; Elena Lundberg; Tadej Battelino; Berit Kriström; Tomasz Giemza; Hichem Zouater
Journal:  Horm Res Paediatr       Date:  2021-07-07       Impact factor: 2.852

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