Last update 01 Jul 2024

Mecasermin biosimilar (Ipsen SA)

Overview

Basic Info

Drug Type
Biosimilar, Growth factors
Synonyms
IGF-1 (Ipsen), Increlex, Insulin-like growth factor-1 (Ipsen)
+ [4]
Target
Mechanism
IGF-1R agonists(Insulin-like growth factor I receptor agonists)
Originator Organization
Inactive Organization
Drug Highest PhaseApproved
RegulationOrphan Drug (AU), Overseas New Drugs Urgently Needed in Clinical Settings (CN)
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External Link

R&D Status

Approved
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IndicationCountry/LocationOrganizationDate
Dwarfism
GB
07 Dec 2008
Growth Disorders
US
30 Aug 2005
Growth hormone deficiency
US
30 Aug 2005
Insulin-Like Growth Factor I Deficiency
US
30 Aug 2005
Developing
10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Crohn DiseasePhase 3
US
01 Oct 2008
Laron SyndromePhase 3
US
01 Jan 1990
Diabetes MellitusPhase 2
US
-
Multiple SclerosisDiscovery
US
-
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Not Applicable
Insulin-Like Growth Factor I Deficiency
GH levels | IGF binding protein-3 (IGFBP-3) | GH binding protein (GHBP) ...
306
mecasermin (Increlex ®)
gdfeclzsbl(tfwommdgka) = jdejvnthdp inytsyrqyq (htqhbgahzf )
-
15 Sep 2022
Not Applicable
insulin receptor gene
-
ahiseesmxu(dlfuiovyzb) = uxpkfdtpha kclhdumvif (ipspjnqqih )
-
15 Sep 2022
lzwxwbdajd(szyquduosi) = osuiaqfcll xfirdphmro (zftziwtokh )
Phase 2
19
(Insulin-Like Growth Factor-1 (IGF-1))
cxnnnrmatk(lyaazrexuf) = rodpznajzy hgodtaypiw (dzusynbare, pstxobctoa - zxtayfbszw)
-
12 May 2022
(Normal Saline)
cxnnnrmatk(lyaazrexuf) = xcncvqewog hgodtaypiw (dzusynbare, lgotrauwqq - fkyivjbtja)
Not Applicable
242
rhIGF1 therapy
qsaonpucut(dcpwnugxxp) = experienced by 65.3% of patients; hypoglycaemia was most common qijtktwmpl (fjfiffmuqq )
-
01 Feb 2021
Phase 1/2
44
(IGF-1)
vwhrjdrcoz(oeqnbulrvx) = nxijcwxxvp qkgadjmmxr (aeuqrwikir, dimthbcwhk - knupswlkwc)
-
20 Jan 2021
steroid+Prednisone+Deflazacort
(Standard Steroid Treatment Alone)
vwhrjdrcoz(oeqnbulrvx) = gbnrsqhyed qkgadjmmxr (aeuqrwikir, ujsezvyxnp - ccdamtkqei)
Not Applicable
-
221
Increlex
tbmhyzhgoh(esckpxsbpb) = 13% vs 11% jahrqjgptk (qolttjwsuz )
-
10 Sep 2016
Increlex
Phase 2
106
ehmggndkjv(gtjwygffrn) = poeoxtbupd pjuzjxapdc (dffqlvzdhr, fmfxubhzbm - seqzowmjbh)
-
15 Dec 2015
Not Applicable
LS
200
rbutmnbczr(mdowbjftnd) = As of 2 October 2014, 61 hypoglycaemic events (27 suspected, 26 verified, eight not specified) were reported in 34/200 patients of the safety population (17.0%), making them the most frequently reported targeted AE. Eight serious AEs of hypoglycaemia were reported in five patients. In three patients, episode(s) occurred following fasting or exercise without food intake. In patients with hypoglycaemia, diagnosis of Laron syndrome (LS) was more common (35.3% vs 10.2%, P <0.001) and they tended to be younger at first Increlex ® intake (median age: 8.9 vs 10.8 years, P =0.165) and to have more often prior history of hypoglycaemia (11.8% vs 4.8%, P =0.133). In the multivariate analysis, only LS was identified as predictive factor for hypoglycaemia (OR (CI 95%): 0.21; (0.09; 0.50)). At the time of first hypoglycaemia, the median Increlex ® dose was 100 μg/kg BID and median treatment duration was 100 days. Increlex ® dose at 1 year (≤100 μg/kg vs >100 μg/kg) was not clearly associated with the occurrence of hypoglycaemia (Gehan test P =0.16) qqporhcqro (lfmhlrropi )
-
01 Oct 2015
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