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Limited Research

IGF-1 LR3

Modified Growth Factor Analog | Research Chemical Only

IGF-1 LR3 is a synthetic 83-amino acid analog of human insulin-like growth factor-1 that has never been approved for human use in any country. Despite approximately 3x greater potency than native IGF-1 with a 20-30 hour half-life due to reduced IGF-binding protein interaction, no human clinical trials have ever been conducted. The compound is prohibited in competitive sports, carries significant risks including severe hypoglycemia and cancer proliferation, and remains strictly a research chemical for laboratory use only.

Daily dose

20-100mcg (research range)

Frequency

Once daily

Cycle length

4-6 weeks maximum

Storage

-20°C to -80°C (lyophilized)

Key benefits

Approximately 3x more potent than native IGF-1 with 20-30 hour half-life due to reduced IGFBP binding. Promotes both muscle hypertrophy and hyperplasia in animal models.

How it works

Full IGF-1 receptor agonist with reduced IGF-binding protein interaction. N-terminal extension and R3 substitution prevent sequestration, maintaining free circulating levels. Activates PI3K/Akt/mTOR and MAPK/ERK pathways.

Dosage protocols

Goal

Research Beginner Protocol

Dose

20-30mcg · Once daily, post-workout

Route

Subcutaneous injection

Goal

Intermediate Research Use

Dose

40-60mcg · Once daily, post-workout or morning

Route

Subcutaneous or intramuscular

Goal

Advanced Research Protocol

Dose

80-100mcg · Once daily or split AM/PM

Route

Subcutaneous or site-specific IM

Goal

Women's Research Protocol

Dose

10-20mcg · Once daily

Route

Subcutaneous only

Research indications

muscle Growth

Muscle HypertrophyAnimal studies show 15-20% lean mass gains in 4 weeks through satellite cell activation and protein synthesis enhancement. No human data exists.
Anti-Catabolic EffectsPreserves lean mass in cachexia models through ubiquitin-proteasome inhibition. Cancer cachexia rats maintained 30% more muscle versus placebo.
Hyperplasia InductionUnique ability to create new muscle fibers via satellite cell differentiation, not just enlarging existing fibers. Permanent structural changes possible.

tissue Repair

Wound Healing AccelerationPromotes keratinocyte migration, epithelialization, and collagen synthesis. Mouse studies show faster wound closure and reduced scarring.
Ligament/Tendon RecoveryRat MCL injury model showed improved maximum force and stress with enhanced type-I collagen expression. May overcome mechanical unloading effects.
Burn RecoveryChildren with severe burns treated with native IGF-1 showed protein-sparing effects. LR3 variant untested in humans but theoretically more potent.

metabolic

Nutrient PartitioningDirects calories toward muscle rather than fat storage. Inhibits glucose uptake in adipocytes while promoting muscle uptake.
Fat Loss EnhancementPromotes lipolysis and fatty acid oxidation independent of caloric deficit. Particularly targets visceral adipose tissue in animal models.
Insulin Sensitivity (Acute)Short-term use may improve glucose uptake, though chronic exposure causes paradoxical insulin resistance through receptor downregulation.

Administration

injectable
nasal

Interactions

Avoid Combination
Human Growth HormoneCreates excessive IGF-1 levels. HGH already elevates endogenous IGF-1, adding exogenous LR3 amplifies cancer risk and organ hypertrophy.
Use Caution
CJC-1295/IpamorelinBoth stimulate GH/IGF-1 axis. Combined use may cause receptor desensitization and compounded metabolic effects.
Monitor Combination
MK-677MK-677 increases endogenous IGF-1. Monitor for joint pain, water retention, and insulin sensitivity disruption.
Avoid Combination
InsulinSynergistic hypoglycemic effects can be life-threatening. Requires professional medical supervision if combined.
Synergistic
BPC-157Popular healing stack. BPC-157 (250-500mcg 2x daily) with IGF-1 LR3 (40-60mcg daily) may accelerate tissue repair.
Synergistic
TB-500Complementary healing mechanisms. TB-500 (2-5mg weekly) with IGF-1 LR3 enhances recovery through different pathways.
Use Caution
Anabolic SteroidsAmplified anabolic effects but substantially increased health risks including organ hypertrophy and metabolic dysfunction.
Dose Dependent
MetforminMay help mitigate insulin resistance from chronic IGF-1 use, but requires blood glucose monitoring and dose adjustment.
Monitor Combination
CerebrolysinBoth affect growth factor pathways and neuroplasticity. IGF-1 LR3 binds IGF-1 receptors while Cerebrolysin enhances BDNF/NGF. Potential for additive neurotrophic effects - use conservative doses and monitor for signs of excessive stimulation.

Safety notes

CRITICAL: Consume 30-60g fast carbohydrates immediately after injection

Never inject before sleep - overnight hypoglycemia risk

Monitor blood glucose regularly, especially first week

Contraindicated with any cancer history or undiagnosed growths

May cause organ hypertrophy (heart, intestines) with prolonged use

WADA prohibited - will cause failed drug test in athletes

Research studies

Rat Muscle Hypertrophy Study (Florini et al.)

Sprague-Dawley Rats | 2.5mg/kg/day | 4 weeks | 15-20% lean mass increase

Demonstrated 2.5x greater anabolic response compared to native IGF-1. Satellite cell activation and protein synthesis increased by 50% above baseline. Both hypertrophy and hyperplasia observed.

Fetal Sheep Metabolic Study (Children's Hospital Colorado)

Fetal Sheep | 6.6μg/kg/h acute, 1.17μg/kg/h chronic | 90 min to 1 week | Study halted early

Acute infusion suppressed insulin secretion by 66%. Chronic infusion caused 4 animal deaths from hypoglycemia and hypoxemia. Significantly reduced circulating amino acids, particularly BCAAs.

Pig Growth Inhibition Study

Domestic Pigs | 180μg/kg/day | 4 days | Paradoxical growth reduction

Contrary to expectations, decreased average daily gain and food intake. Reduced plasma IGFBP-3, IGF-1, and insulin. Growth hormone dropped 23% with 60% reduction in pulse area.

Guinea Pig Organ Study

Guinea Pigs | 120μg/day | 7 days | No overall growth, organ-specific effects

No significant body weight gain or feed intake changes. Increased fractional weights of adrenals, gut, kidneys, and spleen. Suggests organ-specific rather than systemic growth effects.

Cancer Cachexia Rat Model

Tumor-bearing Rats | 0.3mg/kg/day | 14 days | 30% lean mass preservation

Low-dose IGF-1 preserved lean mass during cancer cachexia, reducing loss from -41.4g to -28.8g versus placebo. Demonstrates anti-catabolic properties even in disease states.

Alzheimer's Mouse Model (5XFAD)

Transgenic Mice | Intranasal LR3 | 7 months | Plaque remodeling without cognitive improvement

Improved body composition and reduced filamentous plaques in cortex. Increased inert plaques and reduced Aβ oligomers, but failed to improve cognitive symptoms. Highlights gap between cellular and functional outcomes.