Bottom line

GHK-Cu (glycyl-L-histidyl-L-lysine-copper(II)) is a naturally occurring tripeptide-copper complex reported in human biological fluids and used as a cosmetic ingredient. Small, mostly manufacturer-associated topical studies report cosmetic skin endpoints, but the evidence base is not sufficient to establish therapeutic benefit. Systemic administration has not been studied in adequate human trials. A recruiting Phase 2 trial (NCT07437586) is evaluating topical GHK-Cu for acute wound healing.

Identity and composition

FieldVerified information
Preferred nameGHK-Cu
Key aliasesCopper peptide GHK, Copper tripeptide-1, GHK, Kollaren, Liver cell growth factor, Glycyl-L-histidyl-L-lysine
Molecular/sequence identityTripeptide: Gly-His-Lys (GHK); forms stable complex with Cu²⁺ as GHK-Cu
Modifications/formLinear tripeptide; exists as copper(II) complex; MW free peptide ~403 Da; copper complex ~464 Da
Stable identifiersPubChem CID 133697840 (registry record — corresponds to a bis(GHK)-copper species, MW ~744 Da, not the 1:1 complex); CAS 49557-75-7 applies to uncomplexed GHK; UNIIs vary by chemical form
Identity caveatsGHK (the free peptide) and GHK-Cu (the copper complex) are distinct entities. Most biological activity requires copper complexation. GHK without copper has different properties. Cosmetic ingredient names include Copper Tripeptide-1 and Copper PCA. CID 133697840 represents a 2:1 (GHK)₂-Cu species with MW ~744.3 Da, not the commonly cited 1:1 complex (~464 Da). No PubChem 2D depiction is available that corresponds unambiguously to the 1:1 GHK-Cu structure. Use of this CID for structure-rendering purposes is deferred pending stoichiometric resolution or a dedicated registry entry for the 1:1 complex.

Development and approval status

JurisdictionStatus and indicationProduct/sourceAs of
United States (FDA)Not approved as a drug. Regulated as a cosmetic ingredient when marketed for topical cosmetic useVarious cosmetic products2026-08-06
European UnionListed in CosIng inventory (inventory entry, not a regulatory approval or safety determination)Various cosmetic products2026-08-06
Regulatory boundaryCosmetic use and therapeutic-drug claims follow different national rules; wound-healing drug development is investigationalN/A2026-08-06

Mechanism and pharmacology

GHK-Cu acts as a signaling molecule that modulates gene expression (up to 4,000 genes in microarray studies). It chelates and delivers copper to enzymes including lysyl oxidase (required for collagen crosslinking) and superoxide dismutase. It promotes collagen, elastin, and glycosaminoglycan synthesis in dermal fibroblasts, modulates metalloproteinases (MMPs) and their inhibitors (TIMPs), attracts immune and endothelial cells to wound sites, and has anti-inflammatory and antioxidant activities. GHK plasma levels decline from ~200 ng/mL at age 20 to ~80 ng/mL at age 60.

Evidence by claim

Claim/indicationStageGradeBest human evidenceMain resultImportant limitations
Anti-aging/skin quality (topical)Marketed (cosmetic)BMultiple cosmetic RCTs: n=71, n=41, n=67 women12-week facial cream: improved skin density, thickness, laxity, reduced fine lines and wrinklesSmall studies, mostly manufacturer-affiliated; cosmetic not drug endpoints
Collagen stimulation (topical)Marketed (cosmetic)DSmall cosmetic biopsy report summarized in narrative reviewsA surrogate collagen signal was reportedPrimary report and complete sample details were not identified; no therapeutic endpoint
Wound healing (topical)Phase 2CPreclinical only for drug-level evidenceAnimal wound healing models (rabbits, rats, pigs)Phase 2 trial (NCT07437586) recruiting as of 2026
Hair growthCosmeticEAnecdotal/marketing claimsNo controlled human trial identifiedUnsubstantiated for drug-level claim

Key studies

StudyDesign/populationExposure studiedEndpoints and resultLimitations
Pickart 2008 (facial cream)DBPC, n=71 women, mild-advanced photoagingGHK-Cu facial cream × 12 weeksImproved skin density, thickness, laxity, reduced fine lines and wrinklesCompany-affiliated; cosmetic not clinical endpoints
GHK-Cu eye cream trialDB, n=41 women, mild-advanced photodamageGHK-Cu eye cream × 12 weeksReduced lines, improved appearance vs placebo and vitamin K creamSmall; manufacturer-affiliated
Cosmetic collagen reportSmall uncontrolled report summarized in narrative reviewsTopical thigh cream for one monthA biopsy-based collagen signal was reportedPrimary report and complete sample details were not identified; surrogate endpoint
NCT07437586 (ongoing)Phase 2, DBPC, split-wound, n=60 healthy adultsGHK-Cu 0.1% topical gel × 14 daysTime to complete re-epithelializationRecruiting; results pending

Dose and administration evidence

Approved labeled regimen

Not applicable: no approved drug label exists. Cosmetic concentration reports are not approved therapeutic regimens.

Studied regimens (not recommendations)

  • Small cosmetic studies described topical creams/serums over 8-12 weeks.

  • NCT07437586 describes 0.1% topical gel for 14 days. These are descriptive study exposures, not recommendations.

What is not established

No established or recommended human dose. Topical cosmetic evidence does not establish a systemic regimen or therapeutic drug use.

Safety

Established label risks

None as a drug. In a grouped cosmetic-ingredient assessment, the Cosmetic Ingredient Review panel concluded that Copper Tripeptide-1 was safe in the present practices of use and concentration described in that assessment. That conclusion is ingredient- and use-specific; it is not drug approval and does not establish the safety of injectable, systemic, differently complexed, or poorly identified material. CosIng inventory listing likewise is not a safety determination or authorization.

Human-study signals

The small published cosmetic studies reviewed did not establish a robust adverse-event incidence. Absence of a reported signal in those studies is not evidence of safety for systemic use or for all copper-peptide formulations.

Unknowns and product-quality risks

  • Systemic safety (injectable or oral) has not been studied in humans.

  • Copper homeostasis: chronic systemic administration could theoretically affect copper balance.

  • Unregulated "research" products may not meet cosmetic or pharmaceutical standards.

Interactions and special populations

No drug-interaction studies. No adequate safety data for pregnancy, lactation, or pediatric populations for systemic use; pregnancy safety of topical use is also not established here.

Regulatory, compounding, and sport notes

  • FDA: Not a drug. Cosmetic ingredient regulated under the Federal Food, Drug, and Cosmetic Act for topical use. No injectable or systemic drug product has FDA approval.

  • WADA: GHK-Cu was not identified by exact name in the 2026 Prohibited List. Exact-name absence does not resolve S0 for an unapproved pharmacological preparation, and cosmetic-ingredient status does not establish governmental approval for systemic therapeutic use. Athletes should verify the exact product, route, and current status.

  • US compounding: FDA's May 2026 503A update listed GHK-Cu, except injectable routes, in Category 1 under evaluation and announced an intent to consult PCAC before the end of February 2027. Category 1 is not approval or a finding of clinical safety or effectiveness.

  • The free peptide (GHK) and copper complex (GHK-Cu) have different biological activities; products should be specified accordingly.

Evidence gaps

  • No systemic (injectable/oral) human pharmacokinetic or safety data.

  • Cosmetic studies are small, often manufacturer-funded, and lack rigorous clinical endpoints.

  • Wound healing data are predominantly preclinical.

  • Optimal copper-to-peptide ratio and formulation stability are not standardized across products.

  • The "master regulator of 4,000 genes" claim is based on microarray data from specific cell types and may not generalize.

Search notes

  • Databases and registries: PubMed, ClinicalTrials.gov, PubChem, FDA Cosmetics, Cosmetic Ingredient Review

  • Search terms: GHK-Cu, copper peptide, glycyl-histidyl-lysine, copper tripeptide-1

  • Last searched: 2026-08-06

  • Inclusion emphasis: Human studies prioritized; distinction between drug-level and cosmetic evidence

Sources

  1. https://clinicaltrials.gov/study/NCT07437586

  2. https://pmc.ncbi.nlm.nih.gov/articles/PMC6073405/

  3. https://www.mdpi.com/1422-0067/19/7/1987

  4. https://onlinelibrary.wiley.com/doi/10.1155/2015/648108

  5. Market-claim context only; not used to substantiate efficacy, safety, or dose: https://www.peptides.org/ghk-cu/

  6. https://journal.hep.com.cn/smab/EN/10.1007/s43393-026-00447-7

  7. https://www.mdpi.com/2079-9284/5/2/29

  8. Johnson W Jr, et al. Safety Assessment of Tripeptide-1, Hexapeptide-12, Their Metal Salts and Fatty Acyl Derivatives, and Palmitoyl Tetrapeptide-7 as Used in Cosmetics. Int J Toxicol. 2018;37(3 Suppl):90S-102S. DOI 10.1177/1091581818807863. https://www.cir-safety.org/sites/default/files/peptides.pdf

  9. US Food and Drug Administration. Bulk Drug Substances Nominated for Use in Compounding Under Section 503A of the Federal Food, Drug, and Cosmetic Act. Updated May 14, 2026. https://www.fda.gov/media/94155/download?attachment=

  10. World Anti-Doping Agency. 2026 Prohibited List. https://www.wada-ama.org/sites/default/files/2025-09/2026list_en_final_clean_september_2025.pdf

Research updates

Join the atlas. Get the evidence updates.

Receive concise notes when peptide evidence, status, or source records change.