Mecasermin

drug
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Also known as Bio-fd&c igf1CEP-151Cg-gf2Cg-igf-1Igf-1ecIncrelexInsulin-like growth factor 1Insulin-like growth factor iMecasermin recombinantMecaserminaMecasermineMechano growth factorMyotrophinNexpure plant-made igf-1Pv-802Pv802Rh-oligopeptide-2Sh-oligopeptide-2Somatomedin c

Summary

Mecasermin (CHEMBL1201716) is an approved protein (ATC H01AC03) targeting INSR and IGF1R; indicated across 17 conditions including hypothyroidism and laron syndrome.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Protein
  • ATC class: H01AC03
  • Targets: 2 (INSR, IGF1R)
  • Indications: 17 conditions
  • Clinical trials: 13

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1201716
NameMecasermin
TypeProtein
Max phase4
ATCH01AC03

Also known as: Bio-fd&c igf1, CEP-151, Cg-gf2, Cg-igf-1, Igf-1ec, Increlex, Insulin-like growth factor 1, Insulin-like growth factor i, Mecasermin, Mecasermin recombinant, Mecasermina, Mecasermine

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
INSRInsulin receptorAgonist0.8%P06213
IGF1RInsulin-like growth factor I receptorAgonist19%P08069

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

Aggregated over 2 target gene(s): INSR, IGF1R.

Top Reactome pathways

16 total, by targets touching each:

PathwayTargetsGenes
PIP3 activates AKT signaling1INSR
Signal Transduction1INSR
Negative regulation of the PI3K/AKT network1INSR
Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R)1IGF1R
IRS-related events triggered by IGF1R1IGF1R
SHC-related events triggered by IGF1R1IGF1R
PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling1INSR
IRS activation1INSR
Signal attenuation1INSR
Insulin receptor signalling cascade1INSR
Signaling by Insulin receptor1INSR
Insulin receptor recycling1INSR
Intracellular signaling by second messengers1INSR
Signaling by Receptor Tyrosine Kinases1INSR
Extra-nuclear estrogen signaling1IGF1R
Respiratory syncytial virus (RSV) attachment and entry1IGF1R

Dominant GO biological processes

GO termTargets
positive regulation of cell population proliferation2
insulin receptor signaling pathway2
positive regulation of cell migration2
positive regulation of protein-containing complex disassembly2
positive regulation of MAPK cascade2
protein autophosphorylation2
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction2
dendritic spine maintenance2
amyloid-beta clearance2
protein phosphorylation2
cell surface receptor protein tyrosine kinase signaling pathway2
positive regulation of receptor internalization1
heart morphogenesis1
regulation of DNA-templated transcription1
receptor-mediated endocytosis1

Indications & clinical

Indications

17 indications (4 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
hypothyroidism4MONDO:0005420EFO:0004705
Laron syndrome4MONDO:0009877MONDO:0015892
diabetes mellitus3MONDO:0005015EFO:0000400
amyotrophic lateral sclerosis3MONDO:0004976MONDO:0004976
Crohn disease2MONDO:0005011EFO:0000384
bone disorder2MONDO:0005381EFO:0004260
hyperinsulinism2MONDO:0002177MONDO:0002177
retinopathy of prematurity2MONDO:0006952EFO:1001158
multiple sclerosis2MONDO:0005301MONDO:0005301
Rett syndrome2MONDO:0010726MONDO:0010726
Noonan syndrome2MONDO:0018997MONDO:0018997
anorexia nervosa1MONDO:0005351MONDO:0005351
disease of the tendon0MONDO:0100010EFO:1001434

4 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 13.

Phase distribution

PhaseTrials
Not specified5
PHASE1/PHASE23
EARLY_PHASE12
PHASE2/PHASE31
PHASE21
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00571727PHASE2/PHASE3COMPLETEDLong-Term Treatment With rhIGF-1 in GHIS
NCT00004700PHASE2COMPLETEDPhase II Long Term, Randomized Study of Recombinant Human Insulin-like Growth Factor I in Children With Hyperinsulinism
NCT00490100PHASE1/PHASE2TERMINATEDTreatment for Growth Failure in Patients With X-Linked Severe Combined Immunodeficiency: Phase 2 Study of Insulin-Like Growth Factor-1
NCT01438086PHASE1/PHASE2COMPLETEDEvaluation of the Safety and Efficacy of Using Insulin-like Growth Factor-1 in Patients With a Heart Attack
NCT02636270PHASE1/PHASE2COMPLETEDIGF-1 Treatment for Individuals With Short Stature Due to PAPP-A2 Deficiency
NCT01329744PHASE1TERMINATEDEffects of IGF-I in HIV Metabolic Disease
NCT03932162EARLY_PHASE1RECRUITINGGene Expression Changes In Young and Geriatric Skin
NCT01834989EARLY_PHASE1UNKNOWNPatellar Tendinopathy - Effect of Training and Enhancement of the Collagen Synthesis by Insulin-like Growth Factor-I
NCT00004419Not specifiedCOMPLETEDStudy of Recombinant Human Insulin-Like Growth Factor I in Patients With Severe Insulin Resistance
NCT00004699Not specifiedCOMPLETEDDose Ranging Study of Recombinant Human Insulin-like Growth Factor I in Children With Hyperinsulinism
NCT01314508Not specifiedWITHDRAWNIncrelex Treatment of Children With Chronic Liver Disease and Short Stature
NCT01446783Not specifiedCOMPLETEDIGF-I Stimulation of Collagen Synthesis in Ehlers-Danlos Patients
NCT01588093Not specifiedCOMPLETEDIGF-I Induced Muscle Glucose Uptake and Interstitial IGF-I Concentrations

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.

38 molecules share ≥1 primary target. Top 38 by shared-target count:

MoleculeSourceStatusShared targets
CRIZOTINIBChEMBL + PubChemPhase 4 (approved)IGF1R, INSR
PazopanibChEMBL + PubChemPhase 4 (approved)IGF1R, INSR
BRIGATINIBChEMBLPhase 4 (approved)IGF1R, INSR
CERITINIBChEMBLPhase 4 (approved)IGF1R, INSR
ENTRECTINIBChEMBLPhase 4 (approved)IGF1R, INSR
FEDRATINIBChEMBLPhase 4 (approved)IGF1R, INSR
NINTEDANIBChEMBLPhase 4 (approved)IGF1R, INSR
SUNITINIBChEMBLPhase 4 (approved)IGF1R, INSR
LESTAURTINIBChEMBLPhase 3IGF1R, INSR
LINSITINIBChEMBLPhase 3IGF1R, INSR
BMS-754807ChEMBLPhase 2IGF1R, INSR
CENISERTIBChEMBLPhase 2IGF1R, INSR
ELLAGIC ACIDChEMBLPhase 2IGF1R, INSR
FORETINIBChEMBLPhase 2IGF1R, INSR
ILORASERTIBChEMBLPhase 2IGF1R, INSR
R-406ChEMBLPhase 2IGF1R, INSR
TOZASERTIBChEMBLPhase 2IGF1R, INSR
AfatinibPubChemApprovedIGF1R, INSR
belumosudilPubChemApprovedIGF1R, INSR
BinimetinibPubChemApprovedIGF1R, INSR
dacomitinibPubChemApprovedIGF1R, INSR
FostamatinibPubChemApprovedIGF1R, INSR
GefitinibPubChemApprovedIGF1R, INSR
IdelalisibPubChemApprovedIGF1R, INSR
regorafenibPubChemApprovedIGF1R, INSR
SelumetinibPubChemApprovedIGF1R, INSR
TrametinibPubChemApprovedIGF1R, INSR
INFIGRATINIBChEMBLPhase 4 (approved)INSR
LAPATINIBChEMBLPhase 4 (approved)INSR
NERATINIBChEMBLPhase 4 (approved)INSR
OSIMERTINIBChEMBLPhase 4 (approved)INSR
SORAFENIBChEMBLPhase 4 (approved)INSR
DOVITINIBChEMBLPhase 3INSR
LINIFANIBChEMBLPhase 3INSR
QUERCETINChEMBLPhase 3IGF1R
OSI-632ChEMBLPhase 2INSR
SU-014813ChEMBLPhase 2INSR
BelzutifanPubChemApprovedINSR