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Study Ref. Design studied treatmentcontrol treatmentpatientsstudy risk of biassample sizes Results

COVID 19 hospitalized meta-analysis

ACTIV-3 (BRII-196 and BRII-198)
 
NCT04501978
RCTamubarvimab/romlusevimab (BRII-196 and BRII-198-Brii Biosciences)placeboCOVID 19 hospitalizedlow
179/183 inconclusive
  • inconclusive 8 % increase in recovery (PE) with a high degree of certainty due to low risk of bias

PE: primary endpoint; (a): to be demonstrated a result must be statistically significant on a primary endpoint (with multiplicity adjustment if necessary);
Study risk of bias assessed for the study primary endpoint(s) or the main endpoints in case of no formally defined primary endpoint(s).