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Hi everyone,

I must admit that I haven't been around for quite a while but I wanted to run

something past you all, maybe you already know about this so excuse me for not

knowing because of my lack of reading posts from you, for that I apologize.

I'm possibly (if they let me) going to be in a study with teleprivar (sp)and

something that they call VX-222. It is a new drug in a phase II study. There

will be 5-10 people here at the UW-Madison and 150 people throughout the USA and

10 other countries. My question is, has anyone heard of this? It's sponsored by

Vertex. It will be a 12, 24, or 48 week treatment, depending on which group I

will be in. I have a lot of other health problems aside from the hepc so I don't

know if I will qualify. It is for genotype 1 people with cirrhosis (which I'm

not sure I have yet) who were responders who relapsed (that's me). I did

treatment from 2010 - 2011, 63 weeks on just the RIBA and IFN.

What do you all think about me being in this study. The last treatment just

about killed me with 10 rbc transfusions because I was sooo anemic. My WBC's

were also VERY low....down to .90....should be above 3.4 or something like that.

Anyway, I would be very much appreciative if anyone can comment on this or if

anyone has been in a study with the new drug, VX-222.

Thanks for reading,

Barb Z

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