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Peptide Protocol

IGF-1 LR3: long-range IGF-1 — systemic anabolic signaling.

Long-arginine-3 IGF-1 analog with 20–30h half-life. Systemic muscle protein synthesis and satellite cell activation. SubQ or IM.

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peppercalc.com · research use only
20–100 mcg
Per Dose
4 weeks on / 4 off
Cycle
SubQ / IM
Route
Once daily
Frequency
Overview

What is IGF-1 LR3?

Native IGF-1 has a plasma half-life of only ~10–12 minutes due to rapid binding by insulin-like growth factor binding proteins (IGFBPs 1–6). IGF-1 LR3 was engineered with an Arg3 substitution and 13-amino acid N-terminal extension that dramatically reduces IGFBP affinity by >1000-fold, allowing the peptide to remain in free, receptor-active form for 20–30 hours after injection.

IGF-1 LR3 activates IGF-1 receptors (IGF1R) throughout the body — stimulating muscle protein synthesis, satellite cell activation and proliferation, glucose uptake, and adipocyte apoptosis. Its systemic distribution distinguishes it from IGF-1 DES, which has more localized site-specific action. It is prohibited by WADA and represents a significant anabolic compound in sports doping research.

IGF1R Systemic Activation
Binds and activates IGF-1 receptors throughout muscle, bone, and connective tissue, stimulating IRS-1/PI3K/AKT and MAPK/ERK anabolic signaling.
Satellite Cell Activation
Promotes skeletal muscle satellite cell proliferation and differentiation — the primary mechanism for new muscle fiber formation and hypertrophy.
Glucose Uptake
Activates GLUT4 translocation and stimulates glycogen synthesis — insulin-like metabolic effects that can cause hypoglycemia at high doses.
Anti-Catabolic
Suppresses protein catabolism and promotes nitrogen retention, supporting recovery and lean mass preservation.
Dosing Protocol

Dosing Schedule

Parameters documented in published preclinical and clinical research.

Research use only. The following documents parameters from published preclinical and clinical research. Not medical advice. Not for human consumption. Consult a licensed healthcare professional before any use.
PhaseDoseFrequencyDurationNotes
Start20–40 mcgPost-workout SubQ/IMDays 1–7Assess glucose response. Post-workout timing with food to manage hypoglycemia risk.
Working dose40–80 mcgOnce dailyWeeks 1–4Post-workout or AM. Max 4-week cycles to prevent receptor desensitization.
Advanced80–100 mcgOnce dailyWeeks 1–4Upper research dose. Hypoglycemia risk increases — have glucose available.
Off cycle——4 weeks minimumEqual on/off cycling essential to prevent IGF1R downregulation.
Safety Profile

Safety & Side Effects

Generally Well Tolerated
Potent systemic anabolic signaling via IGF1R
Long ~20–30h half-life from single injection
Well-characterized mechanism from published growth factor biology
Muscle satellite cell activation for genuine hypertrophic potential
Potential Concerns
Hypoglycemia risk — glucose monitoring essential at higher doses
WADA S2 prohibited (growth factors)
Potential promotion of pre-existing tumor growth via IGF1R
Joint pain and water retention at higher doses
Research use onlyThis page is an educational reference. None of this constitutes medical advice. Consult a qualified professional before any use. All compounds are for research purposes only.
Evidence Base

Academic References

  1. [1]
    Francis GL, et al. (1992). Insulin-like growth factors 1 and 2 in bovine colostrum. Biochem J. 251(1):95–103. PubMed ↗
  2. [2]
    Tomas FM, et al. (1993). Prolonged effects of insulin-like growth factor-I (IGF-I) and truncated IGF-I on tissue growth and glucose metabolism in pigs. J Endocrinol. 137(3):413–21. PubMed ↗
  3. [3]
    Girbau M, et al. (1987). Insulin and insulin-like growth factor I both stimulate metabolism, growth, and differentiation in cultured sympathoadrenal progenitor cells. Proc Natl Acad Sci USA. 84(9):2892–6. PubMed ↗
  4. [4]
    Baserga R. (1994). The insulin-like growth factor I receptor: a key to tumor growth? Cancer Res. 55(2):249–52. PubMed ↗
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