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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
INTRODUCTION: An initial Phase III clinical trial has evaluated the efficacy and safety of biosimilar recombinant human growth hormone (rhGH; Omnitrope(®), Sandoz) in Spanish children with growth hormone deficiency (GHD). At the end of the study, those patients still growing were offered to remain o...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4349959/ https://www.ncbi.nlm.nih.gov/pubmed/25667132 http://dx.doi.org/10.1007/s12325-015-0181-9 |
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author | Borrás Pérez, Victoria López-Siguero, Juan Pedro Martínez, Gabriela Corripio, Raquel Fernández, Juan Manuel Labarta, Jose Ignacio Ferrer, Marta Cabrinety, Nuria Prieto, Pablo Ramón-Krauel, Marta Bosch, Jordi Espino, Rafael Palla Garcia, Margarida Rebollo, Francisco Jose |
author_facet | Borrás Pérez, Victoria López-Siguero, Juan Pedro Martínez, Gabriela Corripio, Raquel Fernández, Juan Manuel Labarta, Jose Ignacio Ferrer, Marta Cabrinety, Nuria Prieto, Pablo Ramón-Krauel, Marta Bosch, Jordi Espino, Rafael Palla Garcia, Margarida Rebollo, Francisco Jose |
author_sort | Borrás Pérez, Victoria |
collection | PubMed |
description | INTRODUCTION: An initial Phase III clinical trial has evaluated the efficacy and safety of biosimilar recombinant human growth hormone (rhGH; Omnitrope(®), Sandoz) in Spanish children with growth hormone deficiency (GHD). At the end of the study, those patients still growing were offered to remain on treatment (as in usual clinical practice), and continued to be monitored. The aim of this study was to determine the adult height achieved by the Spanish children who participated in the initial Phase III clinical trial, and to evaluate the long-term safety of rhGH treatment. METHODS: This study was a multicenter, observational, retrospective follow-up study of patients who participated in the Phase III clinical trial (70 patients recruited). Auxological parameters [including height, height velocity, and their associated height standard deviation scores (HSDS)] were obtained from 39 patients. Safety was assessed by recording any adverse events (AEs). RESULTS: In total, 27 men and 12 women provided auxological data. At the start of the follow-up study, the mean age of the patients was 12.5 ± 2.7 years, mean height was 144.8 ± 13.9 cm and mean HSDS was −1.16 ± 0.63. By the end of the follow-up period, mean height had increased to 163.1 ± 7.6 cm (n = 36; men 165.5 ± 7.8 cm, women 157.6 ± 3.2 cm) and mean HSDS also increased to −1.01 ± 0.59 (n = 36; men −1.07 ± 0.52, women −0.86 ± 0.72). In terms of safety, no treatment-related AEs were reported during the study. CONCLUSION: This cohort of Spanish patients with GHD showed a positive response to rhGH treatment, achieving adult height within the local normal ranges. In addition, rhGH treatment was well tolerated, with no new or additional safety concerns. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12325-015-0181-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4349959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-43499592015-03-11 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 Borrás Pérez, Victoria López-Siguero, Juan Pedro Martínez, Gabriela Corripio, Raquel Fernández, Juan Manuel Labarta, Jose Ignacio Ferrer, Marta Cabrinety, Nuria Prieto, Pablo Ramón-Krauel, Marta Bosch, Jordi Espino, Rafael Palla Garcia, Margarida Rebollo, Francisco Jose Adv Ther Original Research INTRODUCTION: An initial Phase III clinical trial has evaluated the efficacy and safety of biosimilar recombinant human growth hormone (rhGH; Omnitrope(®), Sandoz) in Spanish children with growth hormone deficiency (GHD). At the end of the study, those patients still growing were offered to remain on treatment (as in usual clinical practice), and continued to be monitored. The aim of this study was to determine the adult height achieved by the Spanish children who participated in the initial Phase III clinical trial, and to evaluate the long-term safety of rhGH treatment. METHODS: This study was a multicenter, observational, retrospective follow-up study of patients who participated in the Phase III clinical trial (70 patients recruited). Auxological parameters [including height, height velocity, and their associated height standard deviation scores (HSDS)] were obtained from 39 patients. Safety was assessed by recording any adverse events (AEs). RESULTS: In total, 27 men and 12 women provided auxological data. At the start of the follow-up study, the mean age of the patients was 12.5 ± 2.7 years, mean height was 144.8 ± 13.9 cm and mean HSDS was −1.16 ± 0.63. By the end of the follow-up period, mean height had increased to 163.1 ± 7.6 cm (n = 36; men 165.5 ± 7.8 cm, women 157.6 ± 3.2 cm) and mean HSDS also increased to −1.01 ± 0.59 (n = 36; men −1.07 ± 0.52, women −0.86 ± 0.72). In terms of safety, no treatment-related AEs were reported during the study. CONCLUSION: This cohort of Spanish patients with GHD showed a positive response to rhGH treatment, achieving adult height within the local normal ranges. In addition, rhGH treatment was well tolerated, with no new or additional safety concerns. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12325-015-0181-9) contains supplementary material, which is available to authorized users. Springer Healthcare 2015-02-11 2015 /pmc/articles/PMC4349959/ /pubmed/25667132 http://dx.doi.org/10.1007/s12325-015-0181-9 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Research Borrás Pérez, Victoria López-Siguero, Juan Pedro Martínez, Gabriela Corripio, Raquel Fernández, Juan Manuel Labarta, Jose Ignacio Ferrer, Marta Cabrinety, Nuria Prieto, Pablo Ramón-Krauel, Marta Bosch, Jordi Espino, Rafael Palla Garcia, Margarida Rebollo, Francisco Jose 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 |
title | 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 |
title_full | 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 |
title_fullStr | 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 |
title_full_unstemmed | 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 |
title_short | 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 |
title_sort | 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 |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4349959/ https://www.ncbi.nlm.nih.gov/pubmed/25667132 http://dx.doi.org/10.1007/s12325-015-0181-9 |
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