For informational and research purposes only. Not medical advice. Content is aggregated from public sources. Always consult a qualified healthcare provider.
Healing & Recovery · Comparison

Larazotide vs Vasoactive Intestinal Peptide (VIP)

A neutral, side-by-side comparison of two healing & recovery peptides — their mechanisms, dosing ranges, administration routes, side effects, and research evidence. For research and educational purposes only.

LarazotideVasoactive Intestinal Peptide (VIP)
CategoryHealing & RecoveryHealing & Recovery
Also known asLarazotide acetate, AT-1001, INN-202VIP, vasoactive intestinal polypeptide, PHM-27
EvidenceFDA-approvedInvestigational (in trials)
Dosing range0.25mg–1mg mg, 3x daily (before meals)25mcg–100mcg mcg, Daily intranasal or 1–2x weekly subcutaneous
AdministrationOral (capsule), Subcutaneous injection (research use)Intranasal spray, Subcutaneous injection, Inhalation (nebulized)
Key side effectsHeadache (most commonly reported adverse event in trials), Nausea (mild), Generally well-tolerated — adverse event rate similar to placebo in clinical trialsFacial flushing, Transient hypotension, Nasal irritation (intranasal route), Tachycardia
Cited sources3 references2 references

Key differences

  • Evidence level differs: Larazotide is fda-approved, while Vasoactive Intestinal Peptide (VIP) is investigational (in trials).
  • Administration: Larazotide — Oral (capsule), Subcutaneous injection (research use); Vasoactive Intestinal Peptide (VIP) — Intranasal spray, Subcutaneous injection, Inhalation (nebulized).
  • Dosing units differ: Larazotide is dosed in mg, Vasoactive Intestinal Peptide (VIP) in mcg — they operate at different scales.
  • Frequency: Larazotide is typically 3x daily (before meals); Vasoactive Intestinal Peptide (VIP) is Daily intranasal or 1–2x weekly subcutaneous.
  • Research depth: this profile cites 3 sources for Larazotide vs 2 for Vasoactive Intestinal Peptide (VIP).

How each works

Larazotide

Zonulin upregulation disrupts the tight junction proteins occludin and claudin, allowing paracellular passage of antigens, LPS, and inflammatory triggers into systemic circulation. Larazotide acts as a tight junction agonist by competitively displacing zonulin from its receptor and directly stabilizing tight junction complexes. The Phase 2b CeD trial (N=342) showed larazotide reduced the ratio of lactulose/mannitol (L/M ratio, standard intestinal permeability marker) and improved GI symptom scores versus placebo in actively-challenged celiac patients.

Vasoactive Intestinal Peptide (VIP)

VIP activates VPAC1 and VPAC2 receptors coupled to cAMP, suppressing pro-inflammatory cytokines while promoting Th2 regulatory immune responses and Treg differentiation. In the CIRS/biotoxin illness framework pioneered by Shoemaker, VIP intranasal formulation demonstrates normalization of inflammatory markers and improvement in TGF-β, MSH, and VIP deficiency seen in CIRS patients. Pulmonary vasodilation effects have been studied for PAH.

Read the full Larazotide profileRead the full Vasoactive Intestinal Peptide (VIP) profile

This comparison aggregates public research and structured profile data for informational purposes only. It is not medical advice and does not recommend either compound for human use. Consult a qualified healthcare provider before considering any peptide.