Published in Vaccine Weekly, September 6th, 1999
PRI conducted a Phase II, placebo-controlled, randomized study of healthy volunteers infected with a susceptible strain of Influenza A and has provided preliminary results to BioCryst. The primary efficacy endpoint was the reduction in viral titers in infected subjects. Preliminary results showed a statistically significant result for the primary endpoint and evaluation of safety showed that the drug was...
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Source: Vaccine Weekly (1999-09-06)
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