Agree with first part of sentence, that we will see combo of 3DAAs-only (no SOC) within a year, but disagree the implication that those trials will be out through SVR unless it is BMY pairing. I suspect they will want to do a little more walking (i.e. successful 2 drug combos thru SVR first - which BMY has, but no other company has) before running.
PS One of the VRUS drugs claims to require three mutations in order to create resistance. Do you know number of mutations required to create resistance for BMY NS5A drug? Also, any thoughts on what other factors are at play in breakthrough - e.g. creating mutations in something that is fragile is harder than creating mutations in something that is more flexible and NS5A, by reputation, is more fragile (i.e. a very high percentage of changes are lethal to the virus' ability to replicate).
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