All,
Has anyone ever used a transit compartment model in NONMEM for PK with
multiple doses. We are looking to use ~25 transit compartments (and
thus ~25 DiffEqs in the $DES block). This seems easier for multiple
doses, compared to the mathematical solution detailed in Rada Savic's
2004 PAGE
Dear Group:
I have posed this question to a different list serve as well so apologize in
advance if it is a duplicate message for some of you.
I have sparse data (2-3 levels /patient) for a drug used in demographically
similar patients with the same disease state but the disease in one group