Abstract | BACKGROUND: METHODS: Data were analyzed from participants who received bamlanivimab 700 mg in ACTIV-2 from October 2020 to February 2021. Long COVID was defined as the presence of self-assessed COVID symptoms at week 24. Self-assessed return to pre-COVID health was also examined. Associations were assessed by regression models. RESULTS: Among 506 participants, median age was 51 years. Half were female, 5% Black/African American, and 36% Hispanic/Latino. At 24 weeks, 18% reported long COVID and 15% had not returned to pre-COVID health. Smoking (adjusted risk ratio [aRR], 2.41 [95% confidence interval {CI}, 1.34- 4.32]), female sex (aRR, 1.91 [95% CI, 1.28-2.85]), non-Hispanic ethnicity (aRR, 1.92 [95% CI, 1.19-3.13]), and presence of symptoms 22-28 days posttreatment (aRR, 2.70 [95% CI, 1.63-4.46]) were associated with long COVID, but nasal severe acute respiratory syndrome coronavirus 2 RNA was not. CONCLUSIONS: CLINICAL TRIALS REGISTRATION: NCT04518410.
|
Authors | Teresa H Evering, Carlee B Moser, Nikolaus Jilg, Eunice Yeh, Busola Sanusi, David A Wohl, Eric S Daar, Jonathan Z Li, Paul Klekotka, Arzhang Cyrus Javan, Joseph J Eron, Judith S Currier, Michael D Hughes, Davey M Smith, Kara W Chew, ACTIV-2/A5401 Study Team |
Journal | The Journal of infectious diseases
(J Infect Dis)
Vol. 228
Issue Suppl 2
Pg. S126-S135
(08 31 2023)
ISSN: 1537-6613 [Electronic] United States |
PMID | 37650236
(Publication Type: Clinical Trial, Journal Article, Research Support, N.I.H., Extramural)
|
Copyright | © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: [email protected]. |
Chemical References |
- Antibodies, Monoclonal
- Antibodies, Monoclonal, Humanized
- bamlanivimab
|
Topics |
- Female
- Humans
- Male
- Middle Aged
- Antibodies, Monoclonal
- Antibodies, Monoclonal, Humanized
(adverse effects)
- COVID-19
- Post-Acute COVID-19 Syndrome
|