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A prospective randomized multicenter phase I/II clinical trial to evaluate safety and efficacy of NOVOCART disk plus autologous disk chondrocyte transplantation in the treatment of nucleotomized and degenerative lumbar disks to avoid secondary disease: safety results of Phase I-a short report

The primary endpoint was log-transformed and analysed using a normal linear model and an ANCOVA with hepatic status as factor and log body weight at baseline as covariate

Published in-vitro work commonly uses GHK-Cu in the range of 10 nM to 10 M, with 1 M as a frequently reported working concentration

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