BioNTech Results Presentation Deck
BNT162b2 Phase 3 trial
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Vaccinated group
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BNT
162b2
Up to 44,000 participants
21 days
apart
Healthy participants
18-85 (+16-17,12-15) yrs of age
Active surveillance
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for potential COVID-19 symptoms TRIGGERING telehealth or in-
person visit and nasal swab
Number of confirmed COVID-19 cases
≥ day 7 post dose 2
Placebo group
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Interim analysis of unblinded data by independent data monitoring committee on
Nov 8, 2020:
94 disease cases accrued, split of disease cases indicates >90% Vaccine Efficacy
Benign safety profile
Final efficacy analysis at 164 disease cases expected end of November, 2020
Vaccinated participants will continue to be monitored for up to 2 years
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Primary Efficacy Objectives
Efficacy against confirmed COVID-19
in participants without evidence of
infection before vaccination
Efficacy against confirmed COVID-19
in participants with and without
evidence of infection before
vaccination
43,538 participants enrolled
38,955 received 2nd dose
Race/Ethnicity
Asian
Black
Hispanic/Latinx
Overall
Study
5%
10%
26%
Native American
Data as of November 08th, 2020
0.8%
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