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After four weeks on the 1 mg dose, the dosage may be increased again to 2 mg if needed for further glycemic control in patients with Type 2 diabetes

Safety and Tolerability: To address our secondary objectives of safety and tolerability, adverse events were monitored throughout the study based on prior studies (18,19) via medical history, vital signs, physical examination, and standard laboratory assessments (hematology, biochemistry, coagulation, urinalysis)

Subsequently, HaCaT keratinocytes viability after treatment with test compounds, GHK, CuCl 2 and Cu(OAc) 2 were assessed using MTT assay and LDH assay

USA 108 , 1145211457 (2011)

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