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PreclinicalNot FDA-approved

IGF-1 LR3

Modified long-acting IGF-1 analog

Also indexed as: Long-R3 IGF-1

What this evidence does not tell us

Animal organ-growth research and analytical identification of a product are not clinical efficacy trials. LR3 is not mecasermin, an approved IGF-1 medication.

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7 glossary terms used in this profile

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Definitions explain the words—not whether a molecule works or is safe. Research education only, not medical advice.

Overview

IGF-1 LR3 is a modified insulin-like growth factor analog used in experimental research. It is not interchangeable with native IGF-1 or the approved medication mecasermin.

Mechanism of action

IGF-1 receptor signaling

Activates IGF-1 receptor signaling with altered interactions with IGF-binding proteins compared with native IGF-1. Experimental effects on growth and metabolism are not proof of safe human use.

A biological pathway describes a proposed or observed interaction—not necessarily a demonstrated health outcome.

Decode the terminology in our glossary

Scientific evidence

How strong is the evidence?

Early lab & animal research

  1. Limited evidence
  2. Early researchCurrent category
  3. Human research
  4. Human outcomes

Most support comes from cells or animals. These studies help form questions, but do not prove a treatment works in people.

For this research: Animal organ-growth research and analytical identification of a product are not clinical efficacy trials. LR3 is not mecasermin, an approved IGF-1 medication.

An editorial guide—not a validated score, a percentage, a safety rating or an approval badge. Regulatory status is separate. More research does not mean fewer risks.

Cell studies

Mechanistic laboratory evidence is not separately assessed in this selected-source summary; see references and their study types.

Animal experiments

The cited guinea-pig study measures organ growth and IGF-binding proteins.

Human observational studies

Associations, biomarker studies and anecdotes cannot establish treatment causality; no observational result is used here to infer clinical effectiveness.

Human clinical trials

Reliable, independently replicated human outcome evidence is not established by the selected sources in this edition.

Regulatory evidence

No FDA-approved finished drug for this molecule is identified in this edition. Investigational use, published research or compounding does not establish FDA approval.

Potential research applications

Growth-factor signaling in cell culture and animal models.

These describe scientific questions, not prescribing recommendations. A research grouping does not establish combination safety or clinical effectiveness.

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Safety considerations

IGF signaling can affect glucose and growth pathways; hypoglycemia and unintended tissue growth are concerns. Human safety for this analog is not established.

This is not an exhaustive safety or contraindication list. An absence of reported harm is not proof of safety. Pregnancy, breastfeeding, cancer history, endocrine disease and concurrent medicines can materially change risk. Unregulated preparations add identity, contamination and sterility risks.

Regulatory status · United States

Not FDA-approved

No FDA-approved finished drug for this molecule is identified in this edition. Investigational use, published research or compounding does not establish FDA approval.

Regulatory status and evidence strength are different. A nomination for compounding, a clinical-trial registration or a “research use only” label is not approval. International rules vary; consult the current regulator and product label.

Selected literature & source transparency

Cell / animal study· 1995

Long R3 insulin-like growth factor-I (IGF-I) infusion stimulates organ growth but reduces plasma IGF-I, IGF-II and IGF binding protein concentrations in the guinea pig.

The Journal of endocrinology

Analytical study· 2010

Detection of His-tagged Long-R³-IGF-I in a black market product.

Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society

Matched bibliographic records confirm a publication’s identity, not the validity of every claim. Selected sources are not a systematic literature review.

Continue your own source search

These open search results, not additional verified citations. Trial registration is not evidence that a treatment works.

Three questions worth bringing to your clinician

  1. Which human outcomes—not just biomarkers—support this claim?
  2. What established options address my actual health concern?
  3. What do my medical history and current medicines change about the risks?

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Education, not a prescription. Research summaries are not medical advice, dosing instructions, or an offer to sell. Mechanistic findings do not establish clinical effectiveness. US regulatory status is product- and indication-specific and may change. Discuss health decisions with a licensed clinician.