⚠️ Research Use Only — Compounds discussed are research chemicals, not FDA-approved for human use. Not medical advice. Full disclaimers →
Also known as: Insulin-like Growth Factor 1 Long R3
IGF-1 LR3 is a growth factor research compound (not FDA-approved for human use) studied for muscle growth. IGF-1 LR3 is a long-acting analog of Insulin-like Growth Factor 1 studied for its ability to trigger new muscle cell creation (hyperplasia) beyond what training alone can achieve. Research dose: 50–50 mcg 5x/wk. Half-life: 20 hours. Available from COA-verified vendors with code PEPTIDEX for up to 20% off.
Rankings independent · Research use only
IGF-1 analog with extended half-life for muscle cell hyperplasia (new cell creation, not just hypertrophy). Promotes nitrogen retention and protein synthesis.
COA-verified vendors · Use code PEPTIDEX for up to 20% off
* Prices for research peptide acquisition. Not therapeutic products.
| Vendor | Purity | List Price | With PEPTIDEX | Code | Shop |
|---|---|---|---|---|---|
| 99%+ | $69.991 mg | $55.99Save 20% | PEPTIDEX | * Research vendor — verify your regional regulations before purchase. Shop |
Use code PEPTIDEX for 20% off at Amino Club.
* Research vendor — verify your regional regulations before purchase.
Shop at Amino ClubIGF-1 analog with extended half-life for muscle cell hyperplasia (new cell creation, not just hypertrophy). Promotes nitrogen retention and protein synthesis.
IGF-1 LR3 demonstrates significantly enhanced potency over native IGF-1 due to reduced binding protein affinity and extended half-life, promoting dose-dependent muscle growth.
PreclinicalPhilippou & Barton (Growth Hormone & IGF Res.): Comprehensive review of IGF-1's role in muscle satellite cell activation, myoblast proliferation, and skeletal muscle regeneration.
PreclinicalBowers et al.: Meta-analysis of epidemiological studies examining positive correlation between circulating IGF-1 levels and prostate, breast, and colorectal cancer risk.
Moderate-StrongA 2025 study found that a novel plant-based nerve conduit featuring controlled release of IGF-1 LR3 significantly improved axonal regeneration in a rat model of sciatic nerve injury. The conduit demonstrated performance comparable to autologous nerve grafts without inducing systemic toxicity.
PreclinicalA 2025 study found that a one-week infusion of IGF-1 LR3 did not improve growth or insulin secretion in growth-restricted fetal sheep. However, the treatment demonstrated a reduction in circulating amino acids, suggesting increased amino acid utilization.
PreclinicalA 2025 study found that intranasal LR3-IGF-1 promoted amyloid plaque remodeling and reduced low molecular weight Aβ oligomers in the cerebral cortex of an Alzheimer's mouse model. However, the treatment failed to preserve cognitive function or memory in the mice.
PreclinicalA 2024 study demonstrated a simplified, validated chromatographic-mass spectrometric method for efficiently extracting and detecting prohibited peptides, including insulins and GHRHs, in doping control urine samples. The approach successfully met World Anti-Doping Agency requirements and was verified using authentic post-administration samples.
PreclinicalA 2023 study found that an IGF1 analog mitigated age-related loss of gastric pacemaker cells in mice by activating ERK1/2 signaling. This preservation demonstrated improved gastric compliance, increased food intake, and prevented impaired body weight gain in the animal model.
PreclinicalIn a 2023 study, researchers demonstrated that high levels of bioactive human IGF-1 and its analog LR3 IGF-1 can be successfully produced in a Pichia pastoris expression system by fusing them with xylanase. The purified recombinant proteins exhibited excellent cell proliferation bioactivity comparable to standard IGF-1.
PreclinicalA 2023 study demonstrated that acute IGF-1 LR3 infusion in fetal sheep suppressed in vivo glucose-stimulated insulin secretion. However, researchers found that isolated islets retained the ability to recover insulin secretion in vitro, indicating beta-cells can overcome acute suppression.
PreclinicalPotent; use caution. Risk of hypoglycemia. Theoretical cancer promotion concern well-documented in literature. Research-only.
See our evidence grading methodology for how we evaluate and grade peptide safety data.
* Dosing data from published literature — not a human use recommendation.
Very low doses. Inject post-workout for localized muscle effects. Monitor blood sugar closely. Short cycles only.
Last updated: 2026-01 · Laws change frequently. Verify current status in your jurisdiction.
Week 1
Enhanced nutrient partitioning; increased post-workout pumps
Weeks 2–4
Lean mass and recovery improvements; possible hypoglycemia if undereating
Month 2–3
Significant body composition changes; hyperplasia (new cell creation) possible
Long-term
Theoretical cancer promotion risk with chronic use; short cycles essential
| Side Effect | Incidence | Severity |
|---|---|---|
Hypoglycemia Especially if dosed without food nearby; have glucose on hand | ~10% of users | moderate |
Joint pain | ~8% of users | mild |
Headache | ~5% of users | mild |
Fluid retention | ~10% of users | mild |
Finding verified, high-purity IGF-1 LR3 requires rigorous COA verification. We independently evaluate vendors based on third-party HPLC testing, purity thresholds (≥98%), and batch-specific documentation.
View COA-Verified IGF-1 LR3✓ Third-party tested·✓ US shipping·✓ COA on every batch
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Maximize absolute lean muscle gain through sustained GH optimization and direct muscle cell hyperplasia
⚠️ Educational only · Not medical advice · For research use only. Information on this page is compiled from peer-reviewed literature and is intended strictly for educational and informational purposes. Peptides discussed may be unapproved research chemicals — consult a licensed healthcare professional before considering any peptide compound. Read our full disclaimer
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PeptiDex Research is the byline used by the independent researcher who builds and maintains PeptiDex. The site is a one-person research project — there is no editorial board, no medical reviewers, and no clinical staff. Content is produced by reading...
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