Onset
Not established for this analogue.

Protocol / Research Dosing Guide
An evidence-organized IGF-1 LR3 reference that keeps research-community practice clearly separated from what published human research supports.
IGF-1 LR3 is an engineered IGF-1 analogue modified so that it escapes most binding-protein capture, which extends its activity compared with native IGF-1. There is no approved human use and no dose-finding trial. The amounts discussed online are research-community practice, and the main documented hazard is hypoglycemia from insulin-receptor cross-activity.
Why researchers care
Anabolic signalling, tissue growth and recovery research
Class
Long R3 insulin-like growth factor 1, a modified IGF-1 analogue with reduced binding-protein affinity
Route reported
Subcutaneous or intramuscular in reported practice
Cycle length
Reported multi-week community blocks; not validated
Regulatory status
Not FDA approved
The supplied source reports subcutaneous and intramuscular research-community ranges, community cycle structures, half-life claims and a 1 mg vial with 2 mL of bacteriostatic water as a calculator example. It presents these as observational, not as guidance.
| Phase or study | Amount | Frequency / evidence |
|---|---|---|
| Community reported block | Multi-week daily use described in community protocols | Community reported |
| Community reported frequency | Once daily is the most commonly described pattern | Community reported |
| Human validated schedule | Not established | Not established |
| Rest period | Community blocks describe off periods; no trial validates them | Not established |
No human study establishes an IGF-1 LR3 amount, frequency, block length or rest period. Everything reported here is observational.
Neutral research-material planning only. This does not establish an appropriate amount or route.
Research planning item
Exact labeled research vial
Research planning item
Bacteriostatic water at a measured volume
Research planning item
U-100 insulin syringes for very small draws
Research planning item
Alcohol prep swabs
Research planning item
Sharps container
Research planning item
Refrigeration for the prepared vial
Research planning item
Glucose monitoring capability given hypoglycemia risk
Concentration
0.5 mg/mL
Draw volume
0.08 mL
U-100 units
8
Mathematical draws
25
Arithmetic only. The entered amount is not a recommendation and does not establish suitability.
Not established. Community descriptions vary and no study compares timing.
A community rationale, not a tested variable.
Community sources commonly describe carbohydrate availability because of hypoglycemia risk; this is a caution, not a protocol.
No validated procedure exists.
| Format | What is reported | Evidence limit |
|---|---|---|
| Subcutaneous | The most commonly described research-community route | No human pharmacokinetic study for this analogue |
| Intramuscular | Also described in community practice | Site-specific claims are not supported by evidence |
| Oral | Not viable | A protein of this size is destroyed by digestion |
Routes and amounts are not interchangeable unless a verified study explicitly establishes a conversion.
| Measure | Finding | Evidence limit |
|---|---|---|
| Reported analogue half-life | Community sources describe a substantially longer active window than native IGF-1 | Not confirmed by a human study |
| Native IGF-1 comparison | Native IGF-1 is largely bound by binding proteins | The LR3 modification reduces that binding |
| Human pharmacokinetics | Not established | No human study identified for LR3 |
| Frequency logic | Once-daily use is a community convention | Not experimentally validated |
| Route | Amount | Frequency | Source | Human validation |
|---|---|---|---|---|
| Subcutaneous | Community reported micrograms per day | Once daily | Community report | No |
| Intramuscular | Community reported micrograms per day | Once daily | Community report | No |
| Human validated | Not established | Not established | No evidence | No |
Published study values describe those studies. Community-reported values are not validated dosing recommendations.
Concentration: 0.5 mg/mL
| Entered amount | Volume | U-100 units |
|---|---|---|
| 0.04 mg | 0.08 mL | 8 units |
| 0.08 mg | 0.16 mL | 16 units |
| 0.12 mg | 0.24 mL | 24 units |
Reconstitution does not establish identity, purity, sterility, stability, or an appropriate amount.
IGF-1 LR3 activates the IGF-1 receptor and can cross-activate the insulin receptor.
Current status · verified September 16, 2026
Not FDA approved
This is an evidence-gap and precaution list, not an approved prescribing label.
Active or prior cancer
IGF-1 signalling promotes cell proliferation
Diabetes or hypoglycemia risk
Insulin-receptor cross-activity can lower blood glucose
Pregnancy or breastfeeding
No safety data
Children or adolescents
Growth-axis effects are not characterized for this analogue
Retinopathy or untreated endocrine disease
IGF-1 effects on these conditions are not characterized
Important limitation: The most frequently described hazard.
Important limitation: No controlled incidence data.
Important limitation: Consistent with growth-axis effects but not quantified.
Important limitation: IGF-1 signalling drives cell growth; human risk is not quantified.
Important limitation: No interaction studies for this analogue.
Important limitation: No follow-up evidence.
Not established for this analogue.
Multi-week structures are reported without validation.
Blood glucose awareness is the most frequently cited caution; no validated monitoring protocol exists.
Not established.
| Claim | Evidence level | What research shows | Important limitation |
|---|---|---|---|
| Muscle or tissue growth | Not established in humans | Community reported | No human trial |
| Recovery | Not established in humans | Community reported | No human trial |
| Cell-culture proliferation | Established in laboratory use | Level 2 | Not a human outcome |
| Fat loss | Not established | Community claim | No evidence |
Follow the product label; keep cool, dry and out of light.
Refrigerate; no validated LR3-specific stability window was identified.
Repeated freeze-thaw cycles are avoided for protein solutions.
Cloudiness, discoloration or particles mean the solution should not be used.
That is expected at 1 mg per vial; use a 0.3 mL U-100 syringe for readable units.
These are classic low-blood-sugar symptoms; treat glucose first and seek clinical review.
Concentration differs with the liquid volume added; recompute from your own vial.
Stop and seek qualified product guidance.
No validated procedure exists.
| Compound | Class or mechanism | Evidence | FDA status |
|---|---|---|---|
| IGF-1 LR3 | Binding-protein-resistant analogue | No human trial | Not approved |
| Native IGF-1 (mecasermin) | Recombinant human IGF-1 | Approved for defined deficiency indications | Prescription only |
| IGF-1 DES | Short-acting analogue | Different reported profile | Not interchangeable |
An engineered IGF-1 analogue modified to escape most binding-protein capture.
No.
No dose-finding trial exists.
IGF-1 can cross-activate the insulin receptor and lower blood glucose.
No. Mecasermin is native recombinant IGF-1 and a different product.
0.5 mg/mL, so 40 mcg is 0.08 mL or 8 units on a U-100 syringe.
No evidence supports site-specific growth.
No.
Human risk is not quantified, but IGF-1 signalling promotes cell proliferation.
Concentration and volume arithmetic only.
No.
Coverage source
Supplied coverage source for reported ranges, cycles and vial arithmetic.
Open direct sourceRegulatory labeling
Approved IGF-1 labeling, included as regulatory contrast rather than LR3 evidence.
Open direct sourcePublished research
Published characterization of the LR3 modification and its reduced binding-protein affinity.
Open direct source