Matrixyl (palmitoyl pentapeptide-4)

Also known as: Pal-KTTKS

Not FDA-approved

Last verified: October 30, 2026

At a glance

FDA approval Not FDA-approved No record in Drugs@FDA
Randomized controlled trials 2 of 33 publications on PubMed
Registered clinical trials 0 0 active
Adverse event reports 1 1 classified as serious
  • Matrixyl (palmitoyl pentapeptide-4) is not an FDA-approved drug: Drugs@FDA has no record of it.
  • PubMed lists 33 publications mentioning it, including 2 randomized controlled trials and 2 animal-only studies.
  • No study registered on ClinicalTrials.gov tests it as an intervention.
  • FDA's adverse event system (FAERS) holds 1 report mentioning it; 1 classified as serious. Reports do not prove causation.

Research topics

  • Skin Aging 10
  • Skin 9
  • Fibroblasts 7
  • Collagen 5
  • Cosmetics 5
  • Administration, Cutaneous 3
  • Cell Survival 3
  • Drug Delivery Systems 3
  • Lipopeptides 3
  • Niacinamide 3

Most frequent MeSH subject headings in the latest PubMed records (English, as indexed).

Regulatory status

Drugs@FDA applications

No application found in Drugs@FDA, FDA's database of approved drugs.

Source: Drugs@FDA (openFDA) · verified October 30, 2026 · API query

FDA compounding safety list

Not on FDA's list of bulk drug substances that may present significant safety risks in compounding.

Source: FDA.gov — Category 2 bulk drug substances · verified October 30, 2026

Removal of a substance from a regulatory list does not mean it has been approved. A "research use only" label does not make a product safe or legal for human use.

Scientific publications

  • All publications 33
  • Human (MeSH) 17
  • Animal only 2
  • Clinical trials 2
  • Randomized controlled trials 2
  • Systematic reviews & meta-analyses 0
  • Case reports 1
  • Retracted 0

Counts are PubMed records that mention the peptide in the title or abstract. Categories overlap, and a mention is not the same as testing the peptide as a treatment. Each number opens the exact PubMed search. Effects seen in laboratory or animal studies may not occur in humans. A registered clinical trial does not show that a substance is effective or safe.

Latest publications

Source: PubMed (NCBI) · verified October 30, 2026

Clinical trials

No registered study on ClinicalTrials.gov lists this peptide as an intervention.

Source: ClinicalTrials.gov · verified October 30, 2026

Adverse event reports

Reports
1
Serious
1
With death outcome
0

Most reported reactions

  • Abdominal discomfort 1
  • Adrenal mass 1
  • Arthralgia 1
  • Arthritis 1
  • Back pain 1
  • Bursitis 1
  • Cataract operation 1
  • Cortisol abnormal 1
  • Decreased appetite 1
  • Diarrhoea 1
  • Feeling abnormal 1
  • Hypertension 1

Adverse event reports do not prove that the substance caused these effects. Side effects not listed here may still occur. Reaction terms are MedDRA terms as reported to FAERS.

Source: FDA FAERS (FAERS data as of July 30, 2026) · verified October 30, 2026 · API query

FDA prescribing information

Official US prescribing information. Dosing sections are intentionally not shown.

Source: DailyMed / openFDA

Change history

No changes since monitoring began on October 30, 2026.