Mecasermin
SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS
Also known as: IGF1, increlex, insulin-like growth factor 1, mecasermin recombinant, somatomedin C, Somatomedin-C
Data last refreshed: (DrugCentral release 2024-11-01)
Key facts
Mecasermin is a drug catalogued in DrugCentral. It was first approved by the FDA in 2005. DrugCentral lists 2 molecular targets, including IGF1R and INSR. Recorded indications include Laron-type isolated somatotropin defect.
- Molecular targets: IGF1R and INSR (2 listed in DrugCentral).
- Indications: Laron-type isolated somatotropin defect.
- ATC code: H01AC03 (Somatropin and somatropin agonists).
Indications & contraindications
Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).
Indications (1)
- Laron-type isolated somatotropin defect
Mechanism & targets
Molecular targets (2)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Insulin-like growth factor 1 receptor | IGF1R | agonist | IC50 8.31 |
| Insulin receptor | INSR | unknown | IC50 5.85 |
Regulatory approvals (2)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 2007-03-08 | EMA | — | — | |
| 2005-08-30 | FDA | — | IPSEN INC | Yes |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
H01AC03 | SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS › PITUITARY AND HYPOTHALAMIC HORMONES AND ANALOGUES › ANTERIOR PITUITARY LOBE HORMONES AND ANALOGUES › Somatropin and somatropin agonists |
Pharmacogenomics
Drug-label and guideline annotations from PharmGKB and CPIC.
- EMA label: IGF1
- FDA label: GH1, IGF1
- HCSC label: GH1, GHR, IGF1
Reported adverse-event signals
Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.
| MedDRA term | LLR |
|---|---|
| Tonsillar hypertrophy | 208.8 |
| Hypoglycaemia | 141.8 |
| Product dose omission issue | 83.9 |
| Adenoidal hypertrophy | 77.2 |
| Papilloedema | 53.6 |
| Snoring | 52.5 |
| Injection site pain | 49.3 |
| Injection site urticaria | 46.0 |
| Blood glucose decreased | 45.6 |
| Idiopathic intracranial hypertension | 44.2 |
| Off label use | 41.1 |
Chemical structure
| Molecular formula | — |
|---|---|
| Molecular weight | — |
| CAS number | — |
| InChIKey | — |
| PubChem CID | — |
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
What is Mecasermin used for?
DrugCentral lists the following indications for Mecasermin: Laron-type isolated somatotropin defect.
How does Mecasermin work?
Its molecular targets in DrugCentral include IGF1R (agonist) and INSR.
When was Mecasermin first approved?
Mecasermin was first approved by the FDA in 2005.
Browse: all drugs starting with M · drug guides by category · protein targets A–Z.
Sources
- DrugCentral drug card 5009 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1201716 — compound record and bioactivity
- DrugBank DB01277 — drug record
- FDA UNII 7GR9I2683O — substance identity
- DailyMed: FDA labels for Mecasermin — current prescribing information (label search)
- UniProt P08069 (IGF1R) — target protein
- UniProt P06213 (INSR) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
- PharmGKB / CPIC — pharmacogenomic label annotations
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