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doi: 10.1158/0008-5472.CAN-04-4194
Vial
Amount:100mg
There were 3 co-primary outcomes: time to symptom improvement through 28 days, nasopharyngeal SARS-CoV-2 RNA below the lower limit of quantification (LLOQ) on days 3, 7, or 14, and grade 3 or higher treatment-emergent adverse events (TEAEs) through 28 days
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