IGF-1 LR3

Also called: igf1 lr3, IGF-1 peptide

Clinical reviewer: Jacob Moore, MD · Last checked September 16, 2026

What is IGF-1 LR3?

IGF-1 LR3 is a modified, longer-acting analog of insulin-like growth factor 1 sold online as a research peptide. The only FDA-approved form of IGF-1 is mecasermin (Increlex), approved for a narrow pediatric growth-failure indication with serious warnings; IGF-1 LR3 is not that product, is not FDA-approved, and does not appear on FDA's list of substances nominated for compounding.

What is IGF-1 LR3 and how does it differ from approved IGF-1?

IGF-1 LR3 is a modified, longer-acting version of insulin-like growth factor 1, sold online as a research peptide. The only FDA-approved IGF-1 product is Increlex (mecasermin), a recombinant human IGF-1 approved in 2005 for growth failure in children with severe primary IGF-1 deficiency or growth-hormone gene deletion with neutralizing antibodies [1]. Increlex's label carries warnings for severe hypoglycemia that can lead to seizures, intracranial hypertension, and tonsillar or adenoidal hypertrophy, and notes postmarketing reports of malignant neoplasms in children who received it [1]. IGF-1 LR3 is not that approved product and is not FDA-approved itself.

Is IGF-1 LR3 tested in humans or regulated by FDA?

A 2010 case report found that a black-market injection vial sold as an IGF-1 product actually contained a His-tagged form of "Long-R³-IGF-I," a variant the authors say is "usually produced for biochemical studies"; they concluded its effects "in humans have not been elucidated" and that the product "may rather be a by-product from biochemical studies than synthesized for injection purposes" [2]. IGF-1 LR3 does not appear on FDA's May 2026 list of substances nominated for compounding [3]. Insulin-like growth factor 1 and its analogues are prohibited at all times under the 2026 WADA list [4].

Related terms

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Sources

  1. Increlex (mecasermin) Prescribing Information, DailyMed
  2. Black-market Long-R3-IGF-I case report, Growth Hormone & IGF Research, 2010
  3. FDA, Bulk Drug Substances Nominated for Use in Compounding Under Section 503A, May 14, 2026
  4. WADA 2026 Prohibited List, effective January 1, 2026

This entry is for education and is not medical advice. Talk with a licensed clinician about your own situation before starting, stopping, or changing any treatment.

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