Immune

VIP

Also known as: Vasoactive Intestinal Peptide, Aviptadil

Clinical Trials
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Key Facts: VIP

Category
Immune
FDA Status
Not FDA Approved
Clinical Status
Clinical Trials - Multiple indications
Administration
IV infusion, inhaled, or intranasal
Typical Dose
50-100 mcg intranasal daily
Frequency
1-2x daily, intranasal
Duration
Variable by indication
Also Known As
Vasoactive Intestinal Peptide, Aviptadil

Mechanism of Action

VIP works through two G-protein-coupled receptors, VPAC1 and VPAC2, which are spread across immune cells, the gut, blood vessels, and the brain. When VIP binds, the receptor raises intracellular cyclic AMP, and that signal relaxes smooth muscle (so blood vessels and airways dilate) and tamps down inflammatory signaling. On the immune side, that rise in cAMP blunts NF-kB activity and lowers pro-inflammatory cytokines like TNF-alpha, which is the basis for calling VIP an endogenous anti-inflammatory. The same pathway is why researchers looked at it for the runaway lung inflammation seen in severe COVID-19. It is a broadly active hormone, not a targeted single-tissue drug, which is part of why dosing it safely is tricky.

Research Summary

Most of the real human data on VIP comes from aviptadil, the synthetic analog. A randomized controlled trial of intravenous aviptadil in critically ill COVID-19 patients with respiratory failure (about 196 patients, published in Critical Care Medicine in 2022) did not hit its primary endpoint of being alive and free of respiratory failure at 60 days, though there were exploratory signals worth following up. Larger and inhaled formulations were studied through the ACTIV-3b/TESICO program, and the overall picture is mixed rather than a clear win. Beyond the lungs, VIP and its VPAC receptors are studied in rheumatoid arthritis, pulmonary arterial hypertension, and other inflammatory conditions, but that work is largely mechanistic or early-stage. There is no good human evidence supporting the anti-aging, longevity, or general wellness claims VIP is sold for online. Bottom line: a genuinely interesting immune-modulating peptide with real trials, but the trials were in serious illness and did not establish it as an effective therapy.

Trial Progress:Preclinical
Pre
I
II
III
IV
FDA

Dosing Information

Human Trials·Human studies conducted, not FDA approved

Typical Dosing

Community experience

Common Dose

50-100 mcg intranasal daily

Range

25-150 mcg daily

Frequency

1-2x daily, intranasal

Vasoactive intestinal peptide. Used for CIRS/mold illness. Intranasal delivery. Requires proper diagnosis first.

Research Dosing

Scientific studies

Doses from clinical trials

Doses from Studies

50-100 mcg IV for acute conditions

Research Literature - Observed in studies

Duration

Variable by indication

Administration

IV infusion, inhaled, or intranasal

Timing & Administration

Best Time to Take

Morning or as directed

As prescribed

Food Recommendation

With or without food

Why This Timing?

VIP (Vasoactive Intestinal Peptide) affects multiple systems. Timing based on treatment goals.

Possible Side Effects

Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.

  • Nausea and diarrhea
  • Injection site reactions
  • Headache
  • Dizziness
  • Facial flushing
  • Blood pressure decrease
  • Short-lived effects due to instability

References

Research This Peptide Further

Buy in shop

VIP from $81/kit

4 verified vendors, ≥99% purity, COAs included.

Compare prices

Frequently Asked Questions

What does VIP do?

VIP (vasoactive intestinal peptide) is a 28-amino-acid signaling peptide your own gut, nerves, and immune cells make. It is a natural anti-inflammatory and a potent vasodilator, and a synthetic version called aviptadil has been tested in humans for COVID-19 respiratory failure and pulmonary conditions. No VIP product is FDA-approved for the wellness or anti-aging uses it gets marketed for, and most of that human data is in lung disease, not in healthy people.

How does VIP work?

VIP works through two G-protein-coupled receptors, VPAC1 and VPAC2, which are spread across immune cells, the gut, blood vessels, and the brain. When VIP binds, the receptor raises intracellular cyclic AMP, and that signal relaxes smooth muscle (so blood vessels and airways dilate) and tamps down inflammatory signaling. On the immune side, that rise in cAMP blunts NF-kB activity and lowers pro-inflammatory cytokines like TNF-alpha, which is the basis for calling VIP an endogenous anti-inflammatory. The same pathway is why researchers looked at it for the runaway lung inflammation seen in severe COVID-19. It is a broadly active hormone, not a targeted single-tissue drug, which is part of why dosing it safely is tricky.

Is VIP FDA approved?

No, VIP is not currently FDA approved. Current status: Clinical Trials - Multiple indications

What are the side effects of VIP?

Reported side effects include: Nausea and diarrhea, Injection site reactions, Headache, Dizziness, Facial flushing. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of VIP?

Community-reported common dose: 50-100 mcg intranasal daily (1-2x daily, intranasal). Range: 25-150 mcg daily. Administration: IV infusion, inhaled, or intranasal. Community-reported doses. Not medical advice. Consult healthcare provider.

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Enfuvirtide

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PNC27

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PNC-27 is a 32-amino-acid lab-designed peptide that fuses a fragment of the tumor-suppressor protein p53 (residues 12 to 26) to a membrane-penetrating leader sequence. The interesting claim is that it kills cancer cells while leaving normal cells alone, by punching holes in the cancer cell membrane. It is a research compound only, with no approval and no human clinical trials.

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