Wednesday, July 8, 2026

Drug profile · INN

mecasermin recombinant

mecasermin recombinant (INCRELEX) is a insulin-like growth factor i receptor agonist. Route of administration: subcutaneous. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 0
News articles 0
Drug details — mecasermin recombinant
US status
approved
Class
Route
SUBCUTANEOUS
Patents
0
Programs
0
Data quality
0.84

Quick answer

mecasermin recombinant (INCRELEX) is a insulin-like growth factor i receptor agonist. Route of administration: subcutaneous. Current US regulatory status: approved.

Key facts

INN mecasermin recombinant
Brand INCRELEX
Mechanism Insulin-like growth factor I receptor agonist
Target Insulin-like growth factor 1 receptor
Route SUBCUTANEOUS
Formulation INJECTABLE

Mechanism of action

Insulin-like growth factor I receptor agonist

Primary target: Insulin-like growth factor 1 receptor

Approval history

Authority Status Date
FDA approved

Related & competitor drugs

  1. mecasermin Systemic hormonal preparations (H01)
  2. masoprocol Insulin-like growth factor I receptor inhibitor
  3. mecasermin rinfabate recombinant Insulin-like growth factor I receptor agonist
  4. teprotumumab-trbw Insulin-like growth factor I receptor antagonist
  5. mecasermin rinfabate Insulin-like growth factor I receptor agonist
  6. teprotumumab Antineoplastic and immunomodulating agents (L04)

Frequently asked questions

What is mecasermin recombinant?

mecasermin recombinant (INCRELEX) is a insulin-like growth factor i receptor agonist. Route of administration: subcutaneous. Current US regulatory status: approved.

What is the brand name for mecasermin recombinant?

INCRELEX is a marketed brand name for mecasermin recombinant. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of mecasermin recombinant?

mecasermin recombinant has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.