Hi all,
I’ve been having a few issues modeling drugs that suffer from rapid target mediated disposition. Essentially w/severe TMDD we see a 1-2 log drop in first 24-48 hours, then multi-day recovery of serum drug levels and negligible elimination, followed by a first order elimination around day(s) 7-10.
Has anybody successfully modeled these triphasic elimination scenarios in Phoenix? Any tips on the model/compartment structure?
I want to avoid going to Matlab for, well, lazy reasons.
Below is an example using hEPO:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3157300/
Thanks in advance!