Theoretically, it seems to me if 75mg over 24 hours is the therapeutic dose. Dosing 25mg every 8 hours, would keep the dosage at therapeutic levels, and avoid peaks and troughs in serum levels which might allow the virus some wiggle room during the trough phase.
Also, if the medication acts to keep virus from entering cells to replicate (as it has been proven to do in studies of human liver cells transplanted into mice, and also human liver cells in vitro), its role is prophylactic, sort of locking the little buggers down until they die on their own, and/or allowing the DAAs catch them where they live and nuke the shit out of them.
I suppose an analogy would be barring all the entrances and exits to a structure full of HCV, nuking it with DAAs, and then quarantining the survivors where they reside, and laying siege until any survivors simply die off.
If HCV lives outside the body for ~60 days (presumably because that is as long as it can survive without replicating), then it seems that if it is unable to replicate within the body, that ~60 days would be the minimum period to treat with chlorcyclizine, and that twice that would be prudent.
All of this of course is the theory of a layman patient with HCV - so really just thinking out loud, and not in any way intended to be anything beyond pure conjecture.
Failed Interferon 96', G1a, VL = 9 - 5.5 Million, F3/A3, AST 111, ALT 190, Generic DAA treatment Sof/Led (Mylan - India MYHEP LVIR) - 8 June, 2016
2 Week Results 20 June, 2016 AST 19, ALT 32
4 Week Results 06 July, 2016 AST 22, ALT 30, VL = 35
6 Week Results 20, July 2016 VL only = HCV RNA Detected, Non-Quantifiable <15
8 Week Results 04 August 2016, Labs, LFTs Normal, VL = UND
12 Week Results 31 August, 2016 LFTs Normal, VL = UND
EOT + 4 Weeks, LFTs Normal, VL = UND, "SVR4"
SVR12, 21 Nov 2016. CURED!!!