When people are on hepC drug trials through the hospital, their treatment data is recorded for the drug companies.
With so many people going the hepC generic way, won’t this data be lost ?
Male aged 66, contracted hepC 45 years ago
Failed treatment interferon and Ribavarin 2003
Started treatment 22 October 2015, 24 week, Dr Freeman
Sofosbuvir and Ledisbovir plus 12 weeks Ribavirin
Geno 1a
Fibrosis F3/4
VL <12 at 4 weeks
VL – negative at 12 weeks
There are many data points you can record. We will primarily record GT, fibrosis, medications, duration and results @ VL4, SVR4, SVR12.
The goal is simply to answer the question “If I have this GT and this level of fibrosis, what do I take, for how long, to get the best chance of cure?”
Are there any other questions that need answering?
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