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Monograph
PENDING · JUL 2026P-016
Recovery

KPV

Lys-Pro-Val tripeptide. Active C-terminal fragment of α-MSH with potent anti-inflammatory activity in gut and skin tissue.

ExperimentalRecovery
Typical dose200-500 µg
Frequencydaily, oral or subcutaneous
Half-life1h
Citations indexed12
DeliveryInjectable
Half-life~1h
EvidenceExperimental
Citations12
Synergy checkCompareReconstitution calc
Experimental

Evidence is experimental. Most claims trace to limited human studies or animal models. Treat as a research direction, not a protocol.

Mechanism

Three-amino acid tail of alpha-MSH. Suppresses NF-κB signaling and pro-inflammatory cytokines without the pigmentation activity of full α-MSH. Most preclinical work on inflammatory bowel disease and atopic dermatitis. Human RCTs are sparse.

Specifics
Slow wound healingJoint pain
Caveats

Almost no human trial data. Most claims extrapolated from cell-culture and rodent IBD models.

sequence · 3 aa
KPV
Evidence levelExperimental
Regulatory statusFDA Cat. 2 removed Apr 2026 — PCAC review Jul 23-24, 2026
DNA / pharmacogenomicsLow — MC1R variant interest theoretical only.
Claims & evidence

Per-claim grading. Each claim is graded independently — same peptide, different claims can carry different grades.

  • DMechanistic / anecdotal

    KPV — primary mechanism: lys-pro-val tripeptide. active c-terminal fragment of α-msh with potent anti-inflammatory activity in gut and skin tissue.

    1 supporting referencesVerified 5d ago
References

External links to PubMed searches, ClinicalTrials.gov, and FDA materials. We do not host papers — we point at canonical sources.

  • PubMedEN
    REVIEWFunding undisclosedVerified 5d ago
    PubMed — KPV α-MSH
Reconstitution calculatorKPV

Pre-filled with this compound's published dose range: 200-500 µg · daily, oral or subcutaneous

Concentration2.50 mg/mL
Draw volume0.140 mL
Insulin syringe14.0 u
Doses per vial14
U-100 syringe — fill to indicatorU-100 · 1 mL
0u25u50u75u100u

Calculator is a discussion tool. Verify reconstitution + dosing with a qualified provider. Stack is not a prescription source. Use sterile technique and inspect every vial.

PENDING · JUL 2026P-016

FDA Cat. 2 removed Apr 2026 — PCAC review Jul 23-24, 2026

Jul 23, 2026USScheduled reviewUpcoming

PCAC review · July 23-24 2026 panel

FDA's Pharmacy Compounding Advisory Committee scheduled to review the first cohort of peptides removed from Category 2 in April 2026. The 7 peptides on this docket are the highest-profile community names — BPC-157, TB-500, MOTS-c, Epitalon, DSIP, Semax, KPV.

Apr 15, 2026USTier change

FDA removes 12 peptides from Category 2 'significant safety concerns' list

FDA published a Federal Register notice on April 15 2026 removing 12 peptides from the Category 2 ('significant safety concerns') compounding list, paving the way for PCAC review for inclusion on the 503A bulks list. Peptides removed: BPC-157, TB-500, Epitalon, GHK-Cu (injectable), MOTS-c, DSIP, Dihexa Acetate, MK-677, Melanotan II, KPV, Semax, LL-37.

FDA Federal Register · April 15 2026 →
Nov 2023USBan

FDA places peptides on Category 2 'significant safety concerns' list

FDA's Pharmacy Compounding Advisory Committee categorized a wide list of peptides as Category 2 ('significant safety concerns'), effectively banning their compounding at 503A and 503B pharmacies. Affected: BPC-157, TB-500, Epitalon, GHK-Cu, MOTS-c, DSIP, Dihexa, MK-677, Melanotan II, KPV, Semax, Selank, LL-37 and others.

KPV200-500 µg · daily, oral or subcutaneous
Discussion guide, not prescription

stack is an exploration engine. Output is a discussion guide for a conversation with a licensed provider — never a prescription, dose recommendation, or sourcing instruction. Peptides discussed include compounds with limited human evidence and varying legal status by jurisdiction. Verify everything with a qualified clinician before any decision.

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