Hi

 

I have sparse data from n=69 individuals from 3 dose levels, and rich
data from 1 individual at 1 dose level, following the deployment of a
drug eluting device.  In the 69 individuals I have a single plasma
sample, and a single tissue sample (both collected at the same time
point). The sample time points range from 0.25 to 120 days (post
deployment), 2 individuals contributing at each time point. In the 1
individual I have greater than 8 sample points in each biophase.

 

The rich data from the 1 individual suggests 2 compartment disposition
in both plasma and tissue (a 4 compartment model described the data
quite well in WinNonLin). Pooling the sparse data at each dose level,
suggests 2 compartment disposition in both blood and plasma. My
questions are:-

 

1)       Would you take a population approach to this data? - can mean
population parameters and their variability be robustly estimated?

2)       Would you expect the parameters of a 4 cmpt model (8 thetas and
at least 4 omegas) to be reliably estimated with this data?

 

 

Any thoughts much appreciated.

 

Thanks

  

 

Hussain Mulla

 

Department of Pharmacy

University Hospitals of Leicester NHS Trust

Glenfield Hospital

Leicester

England

 

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