<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chew KW</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>NCATS NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH HHS</funding><pagination>131-136</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11793053</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>231(1)</volume><pubmed_abstract>We explored viral and symptom rebound after coronavirus disease 2019 amubarvimab-romlusevimab monoclonal antibody therapy versus placebo in the randomized ACTIV-2/A5401 trial. Participants underwent nasal severe acute respiratory syndrome coronavirus 2 polymerase chain reaction testing at study days 3, 7, 14, and 28. Viral rebound was defined as RNA ≥3 and ≥0.5 log10 copies/mL increase from day 3 or 7, and symptom rebound as hospitalization or any moderate/severe symptom for ≥2 days after initial symptom improvement. There was no difference in viral rebound (∼5%/arm) (analysis population n = 713) or symptom rebound among participants who initially improved (hazard ratio, 0.95 [95% confidence interval, .52-1.75]; analysis population n = 574); &lt;1% had both viral/symptom rebound.</pubmed_abstract><journal>The Journal of infectious diseases</journal><pubmed_title>Viral and Symptom Rebound Following Anti-Severe Acute Respiratory Syndrome Coronavirus 2 Monoclonal Antibody Therapy in a Randomized Placebo-Controlled Trial.</pubmed_title><pmcid>PMC11793053</pmcid><funding_grant_id>U01 AI068636</funding_grant_id><funding_grant_id>UM1 AI106701</funding_grant_id><funding_grant_id>UM1 AI069424</funding_grant_id><funding_grant_id>UM1 AI068634</funding_grant_id><funding_grant_id>UM1AI068636</funding_grant_id><funding_grant_id>UL1 TR001881</funding_grant_id><funding_grant_id>UM1 AI068636</funding_grant_id><funding_grant_id>UM1AI068634</funding_grant_id><funding_grant_id>UM1 AI069419</funding_grant_id><funding_grant_id>UM1AI106701</funding_grant_id><pubmed_authors>Kosmyna J</pubmed_authors><pubmed_authors>Jilg N</pubmed_authors><pubmed_authors>McGinley B</pubmed_authors><pubmed_authors>Murtaugh W</pubmed_authors><pubmed_authors>Evering T</pubmed_authors><pubmed_authors>Eron JJ</pubmed_authors><pubmed_authors>Patel N</pubmed_authors><pubmed_authors>Hughes M</pubmed_authors><pubmed_authors>Smith DD</pubmed_authors><pubmed_authors>Currier JS</pubmed_authors><pubmed_authors>Jennings C</pubmed_authors><pubmed_authors>Singh U</pubmed_authors><pubmed_authors>Gottesman J</pubmed_authors><pubmed_authors>Hosey L</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Riviere C</pubmed_authors><pubmed_authors>Beck J</pubmed_authors><pubmed_authors>Moser C</pubmed_authors><pubmed_authors>Perelson A</pubmed_authors><pubmed_authors>Evering TH</pubmed_authors><pubmed_authors>Margolis D</pubmed_authors><pubmed_authors>Smith DM</pubmed_authors><pubmed_authors>Eron J</pubmed_authors><pubmed_authors>Fischer W</pubmed_authors><pubmed_authors>Wohl DA</pubmed_authors><pubmed_authors>Currier J</pubmed_authors><pubmed_authors>Giganti M</pubmed_authors><pubmed_authors>Daar ES</pubmed_authors><pubmed_authors>Fletcher C</pubmed_authors><pubmed_authors>Hughes MD</pubmed_authors><pubmed_authors>Daar E</pubmed_authors><pubmed_authors>Chew KW</pubmed_authors><pubmed_authors>Newell M</pubmed_authors><pubmed_authors>Sieg S</pubmed_authors><pubmed_authors>Accelerating COVID-19 Therapeutic Interventions and Vaccines (ACTIV)-2/A5401 Study Team, Study Sites, and Investigators</pubmed_authors><pubmed_authors>Gapara M</pubmed_authors><pubmed_authors>Chew K</pubmed_authors><pubmed_authors>Corado K</pubmed_authors><pubmed_authors>Wohl D</pubmed_authors><pubmed_authors>Taiwo B</pubmed_authors><pubmed_authors>Jagannathan P</pubmed_authors><pubmed_authors>Rwakazina I</pubmed_authors><pubmed_authors>Li JZ</pubmed_authors><pubmed_authors>Ritz J</pubmed_authors><pubmed_authors>Javan AC</pubmed_authors><pubmed_authors>Shahkolahi A</pubmed_authors><pubmed_authors>Colsh K</pubmed_authors><pubmed_authors>Pillay S</pubmed_authors><pubmed_authors>Cardoso S</pubmed_authors><pubmed_authors>Roa J</pubmed_authors><pubmed_authors>Pedersen S</pubmed_authors><pubmed_authors>Ignacio RB</pubmed_authors><pubmed_authors>Dragavon J</pubmed_authors><pubmed_authors>Greenfelder B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Viral and Symptom Rebound Following Anti-Severe Acute Respiratory Syndrome Coronavirus 2 Monoclonal Antibody Therapy in a Randomized Placebo-Controlled Trial.</name><description>We explored viral and symptom rebound after coronavirus disease 2019 amubarvimab-romlusevimab monoclonal antibody therapy versus placebo in the randomized ACTIV-2/A5401 trial. Participants underwent nasal severe acute respiratory syndrome coronavirus 2 polymerase chain reaction testing at study days 3, 7, 14, and 28. Viral rebound was defined as RNA ≥3 and ≥0.5 log10 copies/mL increase from day 3 or 7, and symptom rebound as hospitalization or any moderate/severe symptom for ≥2 days after initial symptom improvement. There was no difference in viral rebound (∼5%/arm) (analysis population n = 713) or symptom rebound among participants who initially improved (hazard ratio, 0.95 [95% confidence interval, .52-1.75]; analysis population n = 574); &lt;1% had both viral/symptom rebound.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-06-04T11:03:00.217Z</modification><creation>2026-05-08T03:11:06.27Z</creation></dates><accession>S-EPMC11793053</accession><cross_references><pubmed>39400063</pubmed><doi>10.1093/infdis/jiae501</doi></cross_references></HashMap>