GHK (copper-free tripeptide)

Also known as: Gly-His-Lys · glycyl-histidyl-lysine

Not FDA-approved

Last verified: October 30, 2026

At a glance

FDA approval Not FDA-approved No record in Drugs@FDA
Randomized controlled trials 0 of 163 publications on PubMed
Registered clinical trials 4 3 active
Adverse event reports 2 2 classified as serious
  • GHK (copper-free tripeptide) is not an FDA-approved drug: Drugs@FDA has no record of it.
  • PubMed lists 163 publications mentioning it, including 0 randomized controlled trials and 41 animal-only studies.
  • ClinicalTrials.gov lists 4 registered studies testing it (3 active).
  • FDA's adverse event system (FAERS) holds 2 reports mentioning it; 2 classified as serious. Reports do not prove causation.

Research topics

  • Wound Healing 14
  • Hydrogen-Ion Concentration 13
  • Hydrogels 12
  • DNA 11
  • Skin 11
  • Collagen 10
  • Growth Substances 10
  • Histidine 10
  • Amino Acids 9
  • Electron Spin Resonance Spectroscopy 9

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 163
  • Human (MeSH) 50
  • Animal only 41
  • Clinical trials 0
  • Randomized controlled trials 0
  • Systematic reviews & meta-analyses 0
  • Case reports 2
  • 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

Registered
4
Active
3
With posted results
0

Conditions studied

  • GHK and GHK-Cu Blood Levels 1
  • Aging 1
  • Acute Standardized Cutaneous Wounds (Punch-biopsy Wounds) 1
  • Cutis Laxa Facialis 1
  • Xeroderma 1
Study Status Phase Start
Two-Part Study of the Effects of the X39 Patch on Circulating GHK and GHK-Cu Levels in Healthy Adults
NCT07706361 LifeWave, Inc.
Not yet recruiting N/A Jan 2027
Systemic and Topical Geroprotective Rejuvenation Assessed by START/REST Aging Clocks
NCT07888595 Frontiers in Bioscience Research Institute and Aging
Enrolling by invitation Early phase 1 October 21, 2026
Topical GHK-Cu Gel for Acute Skin Wound Healing
NCT07437586 Hudson Biotech
Recruiting Phase 2 February 2, 2026
Trial Assessing the Impact on Facial Skin Quality, Hydration, and Skin Barrier of Three (3) Hydrafacial Treatments in Adults of All Skin Types.
NCT05932732 Austin Institute for Clinical Research
Completed Phase 4 November 20, 2023

All 4 studies on ClinicalTrials.gov ↗

Source: ClinicalTrials.gov · verified October 30, 2026

Adverse event reports

Reports
2
Serious
2
With death outcome
0

Most reported reactions

  • Adverse drug reaction 1
  • Anaphylactic shock 1
  • Blood pressure decreased 1
  • Flushing 1
  • Heart rate decreased 1
  • Hyperhidrosis 1
  • Hypersensitivity 1
  • Immobile 1
  • Loss of consciousness 1
  • Malignant lymphoid neoplasm 1
  • Pallor 1
  • Product dispensed by unauthorised provider 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.