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IGF-1 LR3

Long R3 IGF-1 · LR3

12 hours
Half-life
20–100 mcg
Typical dose
4–6 weeks
Cycle length

Long-acting IGF-1 analog engineered to resist binding proteins; muscle-growth research compound.

Key takeaways

  • Engineered IGF-1 analog (Arg3 + N-terminal extension) that evades binding proteins.
  • Estimated 12-hour half-life versus minutes for native IGF-1; systemic, not local.
  • Reported community doses run 20–100 mcg daily; no human trials exist.
  • Systemic IGF-1 signaling carries theoretical hypoglycemia and tumor-growth concerns.

Overview

What it is

IGF-1 LR3 (Long R3 IGF-1) is an engineered analog of insulin-like growth factor 1 with an arginine substitution at position 3 and a 13-amino-acid N-terminal extension. Those changes slash binding to IGF-binding proteins, leaving more free hormone to drive anabolic signaling at the IGF-1 receptor.

Pharmacokinetics

The modifications also extend circulation time: the estimated half-life is roughly 12 hours versus minutes for native IGF-1, with around 60% bioavailability. That makes LR3 systemic rather than local.

What the evidence says

Human PK and clinical data are essentially absent. What is known comes from in vitro potency work and animal infusion studies. IGF-1 LR3 is not an approved medication, and community dosing is anecdotal.

Reported dosing protocols

Protocols reported in research literature and clinic/community use — informational context, not a dosing recommendation.

Use case Dose Route Frequency Duration
Muscle growth (community) 20–50 mcg (up to 100) SubQ or IM Once daily 4–6 weeks

Pharmacokinetic summary

Model tier
Simple (t½ + F, Tmax estimated)
Half-life
12 hours
Bioavailability
60%
Typical dose
0.02–0.1 mg

Frequently asked questions

IGF-1 LR3 vs IGF-1 DES — which is which?

LR3 is the long-acting variant (~12-hour half-life), dosed once daily with systemic exposure. DES is the short-acting variant (~30 minutes), used for local site injection. Neither has human trial data.

Why is IGF-1 LR3 dosed only once a day?

The engineered resistance to IGF-binding proteins extends its half-life to roughly 12 hours, so a single daily injection maintains exposure. Shorter-acting IGF-1 variants need more frequent or site-specific dosing.

What are the main risks of IGF-1 LR3?

The acute risk is hypoglycemia, since IGF-1 cross-reacts with insulin signaling. The long-term concern is theoretical: systemic growth signaling could accelerate pre-existing tumors. No human safety data exists, so the real profile is unknown.

References

Related compounds

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