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Impact of Sickle Cell Trait Hemoglobin on the Intraerythrocytic Transcriptional Program of Plasmodium Falciparum

As we did not fit the model to the data, but rather aimed to construct a toy model that captures the fine dynamic features observed experimentally, some of the parameters were manually varied by orders of magnitude (see full description in Appendix Table S1)

Table 18 provides predicted Pharmacokinetic parameter obtained after compartmental analysis of plasma data for transdermal patch of GHK-Cu for the Batch 11

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Clinical trials extending 68 weeks show acceptable safety profiles with no unexpected serious adverse events