What does Mecasermin do? Benefits and evidence
Prescription IGF-1 approved for rare childhood growth failure; low blood sugar is a major risk.
Also called: Increlex, rhIGF-1, Recombinant human IGF-I, Somatomedin C.
IGF-1 and analogues · Recombinant human IGF-1 replacement · Evidence: Approved drug.
Mecasermin copies human IGF-1 and is approved as Increlex for specific rare causes of childhood growth failure. Adult muscle-building and longevity benefits are unproven. Growth studies and safety registries support its childhood use. It can cause severe low blood sugar and unwanted tissue growth.
- Increlex is approved for children age 2 and up whose poor growth comes from severe primary IGF-1 deficiency. (Drug label)
- In a registry of treated patients, final height improved, especially when treatment began before puberty. (Studied in a trial)
- In a small controlled study, it helped growth in people whose bodies cannot respond to growth hormone. (Studied in a trial)
Uses in the sources
- FDA-approved from age 2 for growth failure due to severe primary IGF-1 deficiency, or GH gene deletion with neutralizing GH antibodies. (Drug label) (source)
- Studied for ALS, Rett syndrome, Phelan-McDermid syndrome, diabetes and other conditions. These are not FDA-approved indications. (Studied in a trial) (source)
- Bodybuilding forums discuss Increlex, often confusing it with LR3 or an IGF-1/IGFBP-3 complex. Benefits and product identity are uncertain. (Reported by users) (source)
Related to Mecasermin
- IGF-1 LR3: An unapproved growth signal with no human trials found.
- Somatropin: Prescription human growth hormone, with no proven anti-aging benefit.
Sources
- Bulk Drug Substances Used in Compounding Under Section 503A of the FD&C Act, FDA · FDA · 2026
- Compounding and the FDA: Questions and Answers, FDA · FDA · 2026
- Purple Book Search, FDA · 2026
- The 2026 Prohibited List, World Anti-Doping Agency · WADA · 2026
- Therapeutic Goods (Poisons Standard—October 2026) Instrument 2026, Australian Government · Australian Government · 2026
- INCRELEX (mecasermin) current prescribing information, revised October 2025, Eton Pharmaceuticals, Inc. · DailyMed / Eton Pharmaceuticals · 2025
- INCRELEX (mecasermin) injection, for subcutaneous use, U.S. Food and Drug Administration · FDA · 2025
- INCRELEX (mecasermin) injection, for subcutaneous use, U.S. Food and Drug Administration · FDA · 2024
- Notice to Compounders: Changes that affect compounding as of March 23, 2020, FDA · 2020
- Tailor Made Compounding LLC - 594743 - 04/01/2020, FDA · FDA · 2020
- AusPAR: Mecasermin, Therapeutic Goods Administration
- Increlex, European Medicines Agency
- Increlex, INN-mecasermin, European Medicines Agency
- Know When to Go to the ER, American College of Emergency Physicians · American College of Emergency Physicians
- Mecasermin (Increlex▼): risk of benign and malignant neoplasia, MHRA
Sources checked: 2026-10-18.
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