You highlighted the salient points from the webcast. Here are my own thoughts:
The notion that one or more nukes will form the backbone of HCV combination therapy is based on the immense success this approach has had in the HCV arena (e.g. GILD’s Truvada is a combination of two nukes). Thus, I don’t think Price’s comment in this regard was unduly biased by the fact that VRUS owns the most advanced HCV nuke.
That’s right—almost any combination of direct antivirals from multiple classes will do a good job of stopping HCV viral replication. The key to a medically and commercially successful regimen is thus safety, tolerability, and complementary barriers to resistance by the cocktail components.
By and large, investors don’t yet seem to understand that a great HCV cocktail need not consist of component drugs that are individually great when used with interferon and ribavirin.
R7128 did show kidney tox in monkeys, so it’s not out of the woods yet on safety. The phase-2 R7128+SoC trial includes a preliminary mini-trial in which a few patients in each trial arm are checked for kidney abnormalities before the main portion of the trial can be fully enrolled.
I don’t think this is a major drawback insofar as HCV PI’s are predominantly BID drugs and the dosing schedule of the most-frequently dosed drug in the cocktail is, for all practical purposes, the dosing schedule of the cocktail itself. A bigger issue with R7128 than the BID dosing is the very large 2,000mg/day daily load needed for efficacy, which may preclude R7128 from being co-formulated into an Atripla-like, all-in-one pill.