L-Alanyl-L-Histidyl-L-Lysine Copper(II) Complex (Copper Tripeptide-3)
Synthetic copper-binding tripeptide with one direct laboratory study demonstrating ex vivo human hair follicle elongation and cultured dermal papilla cell proliferation; no clinical trials have been identified (PMID 17703734;).
Last updated: 2026-03-09
No formal adverse event data exists for AHK-Cu from clinical trials. The FDA FAERS and ClinicalTrials.gov files in this project contained no peptide-specific matches. Side effect information is derived from community reports and commercial sources (;;). Copper peptides as a class have a long track record of topical safety in cosmetic use, but formal controlled safety trials specific to AHK-Cu have not been conducted.
uncommon
common
uncommon
rare
Wilson's disease involves impaired copper excretion, and additional copper exposure could worsen copper accumulation. Commercial guidance lists this as a reason to avoid AHK-Cu. General copper peptide safety precaution.
Individuals with known copper allergy should avoid copper-containing peptides.
No safety data exists for AHK-Cu use during pregnancy or breastfeeding. No pregnancy-specific human studies were identified in the supplied trial or FDA search files. General precautionary avoidance recommended (;;).
Low-pH actives may destabilize copper peptides and reduce efficacy. Commercial sources recommend separating application or avoiding concurrent use.
Before considering AHK-Cu, discuss it with your healthcare provider. Ask about potential interactions with your current medications, whether it is appropriate for your health conditions, and what monitoring may be needed.
Sources: [1-2]
Tier 5: All direct evidence for AHK-Cu comes from a single ex vivo/in vitro study (PMID 17703734, Pyo et al. 2007). This study used human hair follicle organ culture (ex vivo) and cultured dermal papilla cells (in vitro). A 2021 narrative review cited the same findings but did not add new controlled human data (PMID 34377956). No animal studies, no Phase 1 or Phase 2 clinical trials, and no randomized controlled trials have been published on AHK-Cu specifically. The ClinicalTrials.gov search returned zero registered trials. The evidence base consists of a single peer-reviewed primary publication with no replication studies.
Pyo HK, Yoo HG, Won CH, Lee SH, Kang YJ, Eun HC, Cho KH, Kim KH - Archives of Pharmacal Research (2007) - ex vivo and in vitro study - Isolated human hair follicles (ex vivo organ culture) and cultured human dermal papilla cells; exact counts not stated in the abstract
AHK-Cu at 10^-12 to 10^-9 M stimulated elongation of human hair follicles ex vivo and proliferation of DPCs in vitro. The tripeptide-copper complex elevated VEGF production and decreased TGF-beta1 secretion by dermal fibroblasts. At 10^-9 M, AHK-Cu elevated Bcl-2/Bax ratio and reduced cleaved caspase-3 and PARP levels, suggesting anti-apoptotic effects. Annexin V/PI staining showed reduced apoptotic DPCs but the decrease was not statistically significant.
Limitations: Single study with no replication. Ex vivo/in vitro only -- no in vivo human or animal data. Sample sizes for individual experiments not reported in abstract. Statistical significance not achieved for apoptosis endpoint (Annexin V). Published in 2007 with no follow-up studies from the same or other groups.
Sadgrove NJ, Simmonds MSJ - FASEB BioAdvances (2021) - narrative review - Not applicable; review article
The review identifies AHK-Cu as a copper-peptide option in the hair and dermal literature, noting that 'AHK-Cu also yielded the same outcome in vitro, that includes reduced expression of TGF-beta1 and increased hair shaft elongation, increased expression of vascular endothelial growth factor and reduced negative growth factors' (citing PMID 17703734 as ref 27).
Limitations: Narrative review rather than original efficacy trial. AHK-Cu discussion is brief (one paragraph). Does not provide new controlled human data for the peptide.