Aviragen Therapeutics, Inc…today announced top-line data from its double-blind, placebo-controlled Phase 2a study of BTA585 in adults challenged intranasally with respiratory syncytial virus (RSV). The data indicate there was not a significant reduction in the primary endpoint, which was viral load. The overall safety profile of BTA585 was favorable and consistent across treatment groups.
When an anitiviral doesn’t reduce viral load, you have a problem.
“The efficient-market hypothesis may be the foremost piece of B.S. ever promulgated in any area of human knowledge!”