Summary
Despite success in prior trials, GHK-Cu failed to prove more successful than placebo in 511-patient Phase 3 trial. Drug was safe but not efficacious. ProCyte later obtained FDA approval as Class I medical device.
Study Details
Study Design
Phase 3 randomized placebo-controlled trial
Indication
Wound healing
Intervention
Topical GHK-Cu
Species
Human
Sample Size
511 subjects
Tags
SourceClinicalGhk CuPhase3Negative Result
Metrics
Citations
0Evidence QualityN/A
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