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Weekly somapacitan in GH deficiency : 4-year efficacy, safety, and treatment/disease burden results from REAL 3
ID
Sävendahl, Lars
(
Avtor
),
ID
Battelino, Tadej
(
Avtor
),
ID
Højby Rasmussen, Michael
(
Avtor
),
ID
Brod, Meryl
(
Avtor
),
ID
Röhrich, Sebastian
(
Avtor
),
ID
Saenger, Paul
(
Avtor
),
ID
Horikawa, Reiko
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(1,47 MB)
MD5: A8D4D7C5DE5F60BAAF11D2BE43947F2A
URL - Izvorni URL, za dostop obiščite
https://academic.oup.com/jcem/article/108/10/2569/7095611
Galerija slik
Izvleček
Context: Growth hormone deficiency (GHD) in children is currently treated with daily injections of GH, which can be burdensome for patients and their parents/guardians. Somapacitan is a GH derivative in development for once-weekly treatment of GHD. Objective: This work aimed to assess the efficacy and safety of somapacitan, and associated disease/treatment burden, after 4 years of treatment and 1 year after switching to somapacitan from daily GH. Methods: This long-term safety extension of a multicenter, controlled phase 2 trial (NCT02616562) took place at 29 sites in 11 countries. Patients were prepubertal, GH-naive children with GHD. Fifty patients completed 4 years of treatment. Patients in the pooled group received somapacitan (0.04, 0.08, 0.16 mg/kg/week) for 1 year, followed by the highest dose (0.16 mg/kg/week) for 3 years. Patients in the switched group received daily GH 0.034 mg/kg/day for 3 years, then somapacitan 0.16 mg/kg/week for 1 year. Main outcome measures were height velocity (HV), change from baseline in HV SD score (SDS), change from baseline in height SDS, disease burden, and treatment burden for patients and parents/guardians. Results: Changes from baseline in HV and HV SDS were similar and as expected in both groups. Observer-reported outcomes showed that patients and parents/guardians seem to have experienced a reduced treatment burden when switching from daily GH to somapacitan. Most parents/guardians (81.8%) strongly/very strongly preferred somapacitan over daily GH. Conclusions: Somapacitan showed similar efficacy and safety in patients who continued somapacitan treatment and those who switched from daily GH to somapacitan. Once-weekly injections may lead to a reduced treatment burden relative to once-daily injections. A plain-language summary of this work is available.
Jezik:
Angleški jezik
Ključne besede:
childhood growth hormone deficiency
,
growth hormone treatment
,
daily growth hormone
,
somapacitan
,
long-acting growth hormone
Vrsta gradiva:
Članek v reviji
Tipologija:
1.01 - Izvirni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2023
Št. strani:
Str. 2569–2578
Številčenje:
Vol. 108, iss. 10
PID:
20.500.12556/RUL-152415
UDK:
616-053.2
ISSN pri članku:
0021-972X
DOI:
10.1210/clinem/dgad183
COBISS.SI-ID:
154830083
Datum objave v RUL:
24.11.2023
Število ogledov:
756
Število prenosov:
55
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Objavi na:
Gradivo je del revije
Naslov:
The journal of clinical endocrinology & metabolism
Skrajšan naslov:
J. clin. endocrinol. metab.
Založnik:
Oxford University Press, Endocrine Society
ISSN:
0021-972X
COBISS.SI-ID:
60951
Licence
Licenca:
CC BY-NC-ND 4.0, Creative Commons Priznanje avtorstva-Nekomercialno-Brez predelav 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by-nc-nd/4.0/deed.sl
Opis:
Najbolj omejujoča licenca Creative Commons. Uporabniki lahko prenesejo in delijo delo v nekomercialne namene in ga ne smejo uporabiti za nobene druge namene.
Projekti
Financer:
Drugi - Drug financer ali več financerjev
Program financ.:
Novo Nordisk
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