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IGF-1 LR3

A modified IGF-1 that hangs around 20–30× longer than the regular version. Used by athletes for sustained growth signaling.

Research referenceCommunity compiled

Molecular profile

What this material is, and why it has no fixed molecular structure.

Class
Long-R3 analog of IGF-1
Receptor / pathway
IGF-1 receptor
Class from the published analog structure; no small-molecule formula applies.
Research & reference information

This profile compiles research and community-sourced reference information for educational purposes. Information may evolve as research and community knowledge develop. It is not individualized medical advice.

Overview

IGF-1 LR3 (Long R3 IGF-1) is an engineered 83-amino-acid analogue of human IGF-1 featuring an amino acid substitution and a 13-amino-acid N-terminal extension.

What problem it targets: It targets sluggish muscle recovery, plateaued lean muscle accrual, muscular atrophy, and stubborn body fat storage.

What It Does

• Evades inhibitory binding proteins: Does not bind to IGF-binding proteins (IGFBPs), allowing it to remain completely free and biologically active in circulation for over 20 to 30 hours.

• Forces nutrients into muscle tissue: Strongly enhances cellular glucose and amino acid uptake into muscle cells rather than fat tissue, acting as a potent nutrient partitioning agent.

• Stimulates satellite cell proliferation: Drives the creation and fusion of new muscle satellite cells into mature fibers, facilitating long-term muscle remodeling.

• Realistic expectations: Produces intense muscle fullness and pumps within days. Injected once daily; cycles are typically limited to 4 to 6 weeks to prevent receptor desensitization and hypoglycemia.

Reconstitution

Vial sizeBAC water / SolventConcentration
0.1 mg+ 0.2 mL acetic acid0.5 mg/mL
1 mg+ 2 mL acetic acid0.5 mg/mL

Solubility & Preparation Notes

The IGF-1 family has an isoelectric point right around neutral pH (~7.0). In plain BAC water, IGF-1 molecules rapidly unfold, adhere to the glass walls of the vial, aggregate, and degrade within days.

Solution: They require an acidic pH (0.6% acetic acid) to remain stable and biologically active in solution.

Step 1 — Solubilize (The Acid Step):
Draw 0.5 mL of sterile 0.6% acetic acid.
Inject it slowly down the inside glass wall of the vial (never spray directly onto the lyophilized cake).
Gently roll the vial between your palms until the liquid is 100% crystal clear.
Verification: Do not add BAC water while the solution is still hazy or clumped. It must be completely transparent first.

Step 2 — Dilute (The BAC Water Top-Off):
Once completely dissolved and clear, add the remaining volume of standard Bacteriostatic Water required by your dosing math.
Why this works: The acetic acid establishes the charge state needed to break the peptide apart into solution; the remaining BAC water dilutes the acid concentration down so it will not sting or irritate tissue upon injection.

Step 3 — Note on reconstituting the entire vial with Acetic Acid:
Users can choose to reconstitute the entire vial using only 0.6% acetic acid if they prioritize maximum long-term chemical stability (standard practice for extended IGF-1 storage). However, note that injecting an unbuffered, full-acid solution will cause a noticeable local sting and burning sensation at the injection site.

Protocol

PhaseFrequencyDoseNotes
StandardDaily post-workout50 mcgSystemic dose.
Site IMPost-workout25–40 mcg/siteLocal muscle.
OffEqual to on-time–Mandatory. Cycle: 4–6 weeks on, equal time off. Off periods critical, receptor desensitises permanently if skipped. Timing: With food, post-workout; long half-life means hypoglycemia risk all day. Evidence: LR3 is not FDA-approved in any form (mecasermin ≠ LR3); no human dosing data. Women: Direct IGF-1 bypasses GH, so estrogen doesn’t soften it; same growth-signal caution: breast, ovarian, or uterine history. Men: Same growth-signal caution, prostate; watch PSA in men over ~40.

Handling & Stacking

Injection site
IM into recently trained muscle (site enhancement) or SubQ abdomen (systemic).
Storage
Freeze-dried: -4°F. Reconstituted in acetic acid: 36–46°F. Best used within 28 days, otherwise potency gradually fades over ~4 weeks (structure-based estimate, no published data).
Side effects
Hypoglycaemia (keep carbs available). Jaw/finger growth at high doses. Headache, nausea.
What to expect
  • Muscle fullness within days, recovery by 2–4 wks.
  • Hypoglycaemia risk, keep fast carbs handy; off-cycles mandatory.
  • Supply math 0.1mg → 14 vials | 1mg → 2 vials (4-wk @ 50 mcg × 7/wk)
Pairs well with
CJC-1295 No DAC + Ipamorelin (GH-axis support); Tesamorelin (visceral fat reduction); BPC-157 / TB-500 (joint and soft-tissue repair); Tirzepatide (offsets glucose shifts)
Avoid
Active malignancy (promotes growth). Diabetic retinopathy. Take with food (NOT fasted/bedtime, blunts effect)

Safety & Patient Education

Contraindications
Active malignancy Acute critical illness (post-surgical, ICU): increased mortality reported in trials Severe / proliferative diabetic retinopathy Pregnancy and lactation
Warnings
  • Intracranial hypertension with somatropin (papilledema, vision changes, headache, nausea, vomiting) Insulin resistance and new-onset T2DM Fluid retention, edema, carpal tunnel Pancreatitis (rare) IGF-1 elevation above age range carries theoretical malignancy risk 20–30 hour half-life means hypoglycemia risk extends throughout the day.
  • Long-term IGF-1 elevation theoretical malignancy concern.
Drug interactions
Glucocorticoids: blunt GH/IGF-1 response, reassess steroid dose after starting GH Insulin / antidiabetics: GH raises insulin needs; IGF-1 and IGF-1 LR3 cause hypoglycemia, adjust accordingly Levothyroxine: GH lowers free T4, recheck TSH/fT4 quarterly Oral estrogens: blunt GH-stimulated IGF-1, consider transdermal if response is blunted CYP3A4 narrow-TI substrates (cyclosporine, tacrolimus, sirolimus): recheck troughs after starting Anticonvulsants (phenytoin, carbamazepine, phenobarbital): GH may shift seizure threshold; monitor levels
Labs
  • IGF-1 (baseline / Wk 8 / end; you're dosing it directly, so this tracks exposure), Fasting glucose (Wk 0/4/8) Lipid panel (Wk 0/12) Hip/scoliosis exam in pediatrics Out of range?
  • IGF-1 above your age range = too much growth signal → drop the dose.
  • Hypoglycemia is the real acute risk and LR3's long half-life drags it out for hours – dose with food/carbs, keep fast sugar handy; shaky, sweaty, or foggy = treat it right away.
Stop criteria
Severe headache with vision changes (rule out intracranial hypertension) New onset hyperglycemia Persistent edema New-onset hip pain in pediatrics
Patient education
Vials must be refrigerated never frozen (somatropin) Rotate injection sites Report new joint pain Children: report any limp or hip/knee pain immediately Eat carbs after injection, not fasted
References
researchdosing · peptidedosages · PubMed · thepeptidereport · peptides.id · Span 2000 · Weissberger 1991