Moderna 2022 Priorities and Capital Allocation
Safety and reactogenicity are similar between .211 and 1273
boosters
Solicited reactogenicity (through day 7)
100
Solicited local adverse reactions
Solicited systemic adverse reactions
100-
75-
50-
25-
Any Local
Pain
50 μg mRNA-1273
50 μg mRNA-1273.211
50 µg mRNA-1273
50 μg mRNA-1273.211
Erythema
50 μg mRNA-1273
50 μg mRNA-1273.211
Swelling
Grade 1
50 μg mRNA-1273
50 μg mRNA-1273.211
50 μg mRNA-1273
50 μg mRNA-1273.211
Lymphadenopathy
Slide 18
75-
50-
25-
0
Any Systemic
Grade 2
50 μg mRNA-1273
50 μg mRNA-1273.211
Fever
50 μg mRNA-1273
50 μg mRNA-1273.211
Headache
50 µg mRNA-1273
50 μg mRNA-1273.211
Fatigue
50 μg mRNA-1273
50 μg mRNA-1273.211
Myalgia
Grade 3
50 μg mRNA-1273
50 μg mRNA-1273.211
Arthralgia
50 μg mRNA-1273
50 μg mRNA-1273.211
Nausea/
vomiting
50 μg mRNA-1273
50 μg mRNA-1273.211
Chills
50 μg mRNA-1273
50 μg mRNA-1273.211
Safety summary
The reactogenicity profile was
similar between the two booster
vaccines (.211 n=298, 1273 n=167)
The frequency and types of
unsolicited adverse events were
also comparable, with no serious
events in the .211 group up to 28
days after the booster dose (.211
N=300, 1273 N=171)
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