Mecasermin
Mecasermin is recombinant human insulin-like growth factor-1 (IGF-1), FDA-approved for severe primary IGF-1 deficiency in pediatric patients with growth failure. It bypasses growth hormone receptor defects and directly activates IGF-1 signaling. Outside approved indications, unsupervised use is high risk due to hypoglycemia and potential proliferative signaling concerns.
Safety & legal caution
Educational database only — not medical or legal advice.
Safety
- Hypoglycemia can be severe; dose with carbohydrate intake and clinical supervision.
- Monitor for tonsillar/adenoidal hypertrophy, intracranial hypertension, and slipped capital femoral epiphysis in children.
- Use caution in patients with active or suspected neoplasia due to growth-factor signaling.
Legal / compliance
- Prescription biologic with narrow approved indication (severe primary IGF-1 deficiency).
- Non-prescribed performance/anti-aging use may violate local law, sport rules, and medical standards.
Current literature links
Evidence
No score yet
Safety
Unknown safety profile
Clinical Status
Approved
Last Sync
Not synced yet
Last Reviewed
Not reviewed yet
Dosing
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Pharmacology
Evidence Score
Plain-English Snapshot
Mecasermin is currently categorized as a peptide compound.
Evidence scoring has not been fully computed yet, so interpret this profile as preliminary.
Safety scoring is incomplete. Start conservatively and monitor carefully.
Core mechanism
Exogenous IGF-1 replacement activating IGF1R/PI3K-AKT-MAPK signaling to restore growth and anabolic signaling
Practical Context
Strongest current signals
No indexed study summaries yet.
Elevated caution signals
1 severe/high side effect flag