You seem to miss my point again. I said the FDA saw the data...

  1. 30,695 Posts.
    lightbulb Created with Sketch. 2030
    You seem to miss my point again. I said the FDA saw the data which demonstrated efficacy so granted them Fast Track designation and ODD so it was excellent. If it wasn't then they wouldn't gave granted them, even @Mason14 was impressed with the CR on low dosage but later said management wasn't seeing enough so are increasing the dosage lol. The lead presenter at the conference also mentioned about the efficacy seen on such low dosage, are you questioning whether the clinical trial update for VAXINIA was excellent?
 
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