Table 3.
pwMS and pwNIc who received tixagevimab/cilgavimab who tested positive to COVID-19 during observation follow-up | Total n=32 |
Age (years) | |
Min | 33 |
Max | 67 |
Mean | 49.47 |
SD | 10.75 |
Sex, n (%) | |
Female | 25 (78.1%) |
EDSS | |
Min | 0 |
Max | 6.5 |
Mean | 2.45 |
SD | 1.86 |
DMT n (%) | |
Ocrelizumab | 22 (68.75%) |
Rituximab | 3 (9.38%) |
Fingolimod | 5 (15.63%) |
Siponimod | 1 (3.12%) |
Other | 1 (3.12%) |
COVID-19 n (%) vaccine dose no | |
2 | 2 (6.25%) |
3 | 9 (28.13%) |
4 | 17 (53.13%) |
5 | 4 (12.5%) |
COVID-19 positive n (%) | |
Tixagevimab/cilgavimab during observation window | 32/167 (19.16%) |
Prior to tixagevimab/cilgavimab availability | 15/32 (46.88%) |
Days from administration to COVID-19 positive n (days) | |
Min | 3 |
Max | 178 |
Mean | 99 |
SD | 52.34 |
DMT, disease-modifying therapy; EDSS, Expanded Disability Status Scale Score; pwMS, people with multiple sclerosis; pwNIc, people with neuroimmunological conditions.