Peptide Dosing Protocols — Master Reference Card

Category: protocols Updated: 2026-04-06

Semaglutide: 0.25mg/week start → 2.4mg/week maintenance (STEP 1, PMID 33567185). BPC-157: 250–500mcg/day (rodent studies, no human RCT). Ipamorelin: 100–300mcg/dose × 3 (Grade C).

Key Data Points
MeasureValueUnitNotes
Peptides Covered16compoundsComprehensive reference covering GH peptides, metabolic, tissue repair, cognitive, and longevity peptides
Semaglutide Starting Dose0.25mg/weekFDA protocol: 0.25mg × 4 weeks, then escalate every 4 weeks to 2.4mg/week maintenance (Wegovy)
Tirzepatide Starting Dose2.5mg/weekFDA protocol (Zepbound): 2.5mg × 4 weeks, escalate by 2.5mg/4 weeks to 15mg/week maintenance
BPC-157 Typical Research Dose250–500mcg/dayResearch extrapolation from rodent effective doses; no human clinical dosing established
Ipamorelin Dose100–300mcg/dosePMID 9849822: GH secretagogue; 3× daily preferred for physiological pulse replication
Semax Research Dose300–600mcg/day intranasalRussian clinical standard; 1–3 divided doses via nasal spray
GHK-Cu Topical Dose1–2% concentrationHuman topical studies typically use 1–2% GHK-Cu creams/serums; systemic research dosing is 1–5mg/day SC

Master Dosing Reference — Important Disclaimer

This table is a research reference, not a clinical protocol. Doses marked Grade A are FDA-approved clinical doses. All other entries are research extrapolations, community conventions, or animal study scaling. No research peptide entry in this table has been validated in a human pharmacokinetic or dose-finding study. Use accordingly.

GH Axis Peptides

PeptideRouteStarting DoseTherapeutic DoseFrequencyTypical CycleBreakEvidence Grade
IpamorelinSubcutaneous100mcg200–300mcg3×/day (fasted)8–12 weeks4–8 weeksC
CJC-1295 (no DAC)Subcutaneous100mcg100–200mcg2–3×/day8–12 weeks4–8 weeksC
CJC-1295 (DAC)Subcutaneous1mg1–2mg1×/week8–12 weeks4–8 weeksC
GHRP-2Subcutaneous100mcg100–200mcg3×/day (fasted)8–12 weeks4–8 weeksC
GHRP-6Subcutaneous100mcg100–200mcg3×/day (fasted)8–12 weeks4–8 weeksC
MK-677 (Ibutamoren)Oral10mg15–25mg1×/day12–16 weeks4–8 weeksC

Metabolic Peptides (FDA-Approved)

PeptideRouteStarting DoseTherapeutic DoseFrequencyTypical CycleBreakEvidence Grade
Semaglutide (Wegovy)Subcutaneous0.25mg2.4mg1×/weekOngoing (chronic)None requiredA
Tirzepatide (Zepbound)Subcutaneous2.5mg5–15mg1×/weekOngoing (chronic)None requiredA
Tesamorelin (Egrifta)Subcutaneous1mg2mg1×/dayOngoing (chronic, HIV)N/A (medical)B
AOD-9604Subcutaneous250mcg500mcg1×/day (fasted)12 weeks4 weeksD

Tissue Repair Peptides

PeptideRouteStarting DoseTherapeutic DoseFrequencyTypical CycleBreakEvidence Grade
BPC-157Subcutaneous or oral250mcg250–500mcg1–2×/day4–6 weeks4–6 weeksC
TB-500 (Thymosin β4)Subcutaneous2mg2–5mg2×/week4–6 weeks4–6 weeksC
GHK-CuTopical or SC1% topical or 1mg SC1–2% topical or 1–5mg SCDaily (topical) or 3×/week (SC)8–12 weeks4 weeksB (topical), C (SC)

Cognitive / Nootropic Peptides

PeptideRouteStarting DoseTherapeutic DoseFrequencyTypical CycleBreakEvidence Grade
SemaxIntranasal200mcg300–600mcg2–3×/day10–14 days2–4 weeksB (Russian), C (Western)
SelankIntranasal200mcg250–500mcg2×/day10–14 days2–4 weeksB (Russian), C (Western)
DihexaSubcutaneous (research)None establishedNo safe dose knownUnknownNone establishedNone establishedD

Longevity Peptides

PeptideRouteStarting DoseTherapeutic DoseFrequencyTypical CycleBreakEvidence Grade
EpitalonSubcutaneous or IV5mg5–10mg1×/day10–20 days4–6 monthsC
HumaninSubcutaneous (research)No established doseNo established doseUnknownNone establishedNone establishedC
SS-31 (Elamipretide)IV (trials only)InvestigationalTrial dosing onlyTrial protocolTrial protocolNot applicableB

Evidence Grade Callout

Grade A (FDA-approved doses): Semaglutide, Tirzepatide, Tesamorelin — doses from Phase 3 RCTs; follow prescribing information exactly. Grade B: GHK-Cu (topical human data), Semax/Selank (Russian clinical), SS-31 (Phase 2/3 trials). Grade C: All GH peptides, BPC-157, TB-500, Epitalon — rodent data scaled to humans; community conventions. Grade D: AOD-9604, Dihexa — failed Phase 3 or no human data; no reliable dose guidance.

This table covers a mix of FDA-approved pharmaceuticals (requiring prescriptions), investigational compounds (accessible only via trials), and research chemicals (no regulatory approval). FDA-approved peptides should only be obtained and used with valid prescriptions. Research chemical peptides have no approved human use; this table is for scientific reference only. Nothing on this page constitutes medical advice or a recommended treatment protocol.

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Frequently Asked Questions

How are research peptide doses determined without human clinical trials?

Most research peptide doses are extrapolated from animal studies using allometric scaling — a calculation that accounts for body surface area differences between species. The most common method uses the formula: Human dose (mg/kg) = Animal dose (mg/kg) × (Animal Km / Human Km), where Km values are species-specific constants (rat Km = 6, human Km = 37). This yields human equivalent doses roughly 6–12× lower than the mg/kg dose effective in rats. These extrapolations carry substantial uncertainty and should not be treated as validated clinical doses.

What does 'evidence grade' mean in this dosing table?

Evidence grade reflects the quality of evidence behind the dose recommendation. Grade A = FDA-approved dosing from large Phase 3 RCTs (semaglutide, tirzepatide). Grade B = human clinical trial data, though not necessarily for the specific peptide indication (e.g., ipamorelin Phase 1/2 safety data). Grade C = animal model dosing extrapolated to humans. Grade D = anecdotal community dosing with no systematic scientific basis. Most research peptide doses in this table are Grade C or D — they represent community convention, not validated clinical protocols.

Should research peptide doses be followed exactly?

No. Research peptide dosing tables represent community conventions derived from animal study extrapolations, not validated human clinical protocols. The therapeutic window, toxicity threshold, optimal frequency, and appropriate cycle length for most research peptides are unknown in humans. Starting at the lowest cited dose, monitoring for adverse effects, and proceeding cautiously is prudent — but even this does not substitute for supervised clinical care. Only FDA-approved peptides (semaglutide, tirzepatide, tesamorelin) have evidence-based dose protocols.

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