Responses to a Neutralizing Monoclonal Antibody for Hospitalized Patients With COVID-19 According to Baseline Antibody and Antigen Levels:A Randomized Controlled Trial

التفاصيل البيبلوغرافية
العنوان: Responses to a Neutralizing Monoclonal Antibody for Hospitalized Patients With COVID-19 According to Baseline Antibody and Antigen Levels:A Randomized Controlled Trial
المؤلفون: Jens D, Lundgren, Birgit, Grund, Christina E, Barkauskas, Thomas L, Holland, Robert L, Gottlieb, Uriel, Sandkovsky, Samuel M, Brown, Kirk U, Knowlton, Wesley H, Self, D Clark, Files, Mamta K, Jain, Thomas, Benfield, Michael E, Bowdish, Bradley G, Leshnower, Jason V, Baker, Jens-Ulrik, Jensen, Edward M, Gardner, Adit A, Ginde, Estelle S, Harris, Isik S, Johansen, Norman, Markowitz, Michael A, Matthay, Lars, Østergaard, Christina C, Chang, Anna L, Goodman, Weizhong, Chang, Robin L, Dewar, Norman P, Gerry, Elizabeth S, Higgs, Helene, Highbarger, Daniel D, Murray, Thomas A, Murray, Ven, Natarajan, Roger, Paredes, Mahesh K B, Parmar, Andrew N, Phillips, Cavan, Reilly, Adam W, Rupert, Shweta, Sharma, Kathryn, Shaw-Saliba, Brad T, Sherman, Marc, Teitelbaum, Deborah, Wentworth, Huyen, Cao, Paul, Klekotka, Abdel G, Babiker, Victoria J, Davey, Annetine C, Gelijns, Virginia L, Kan, Mark N, Polizzotto, B Taylor, Thompson, H Clifford, Lane, Christine, Wenner
المصدر: ACTIV-3/TICO Bamlanivimab Study Group & Nielsen, H 2022, ' Responses to a Neutralizing Monoclonal Antibody for Hospitalized Patients With COVID-19 According to Baseline Antibody and Antigen Levels : A Randomized Controlled Trial ', Annals of Internal Medicine, vol. 175, no. 2, pp. 234–243 . https://doi.org/10.7326/M21-3507
Ann Intern Med
Annals of Internal Medicine
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
ACTIV-3/TICO Bamlanivimab Study Group & Østergaard, L J 2022, ' Responses to a Neutralizing Monoclonal Antibody for Hospitalized Patients With COVID-19 According to Baseline Antibody and Antigen Levels : A Randomized Controlled Trial ', Annals of Internal Medicine, vol. 175, no. 2, pp. 234-243 . https://doi.org/10.7326/M21-3507
ACTIV-3/TICO Bamlanivimab Study Group* & Johansen, I S 2022, ' Responses to a Neutralizing Monoclonal Antibody for Hospitalized Patients With COVID-19 According to Baseline Antibody and Antigen Levels : A Randomized Controlled Trial ', Annals of Internal Medicine, vol. 175, no. 2, pp. 234-243 . https://doi.org/10.7326/M21-3507
سنة النشر: 2022
مصطلحات موضوعية: Male, COVID-19/blood, Antibodies, Monoclonal, Humanized, Antiviral Agents, Article, Double-Blind Method, Internal Medicine, Humans, RNA, Viral/blood, Treatment Failure, Adenosine Monophosphate/adverse effects, Antigens, Viral, Aged, Alanine, SARS-CoV-2, COVID-19, General Medicine, Middle Aged, Antibodies, Neutralizing, Antiviral Agents/adverse effects, Adenosine Monophosphate, Antibodies, Neutralizing/adverse effects, COVID-19 Drug Treatment, Antigens, Viral/blood, Antibodies, Monoclonal, Humanized/adverse effects, Alanine/adverse effects, RNA, Viral, Drug Therapy, Combination, Female, Medical Futility, Biomarkers, Biomarkers/blood
الوصف: BACKGROUND: In a randomized, placebo-controlled, clinical trial, bamlanivimab, a SARS-CoV-2-neutralizing monoclonal antibody, given in combination with remdesivir, did not improve outcomes among hospitalized patients with COVID-19 based on an early futility assessment.OBJECTIVE: To evaluate the a priori hypothesis that bamlanivimab has greater benefit in patients without detectable levels of endogenous neutralizing antibody (nAb) at study entry than in those with antibodies, especially if viral levels are high.DESIGN: Randomized, placebo-controlled trial. (ClinicalTrials.gov: NCT04501978).SETTING: Multicenter trial.PATIENTS: Hospitalized patients with COVID-19 without end-organ failure.INTERVENTION: Bamlanivimab (7000 mg) or placebo.MEASUREMENTS: Antibody, antigen, and viral RNA levels were centrally measured on stored specimens collected at baseline. Patients were followed for 90 days for sustained recovery (defined as discharge to home and remaining home for 14 consecutive days) and a composite safety outcome (death, serious adverse events, organ failure, or serious infections).RESULTS: Among 314 participants (163 receiving bamlanivimab and 151 placebo), the median time to sustained recovery was 19 days and did not differ between the bamlanivimab and placebo groups (subhazard ratio [sHR], 0.99 [95% CI, 0.79 to 1.22]; sHR > 1 favors bamlanivimab). At entry, 50% evidenced production of anti-spike nAbs; 50% had SARS-CoV-2 nucleocapsid plasma antigen levels of at least 1000 ng/L. Among those without and with nAbs at study entry, the sHRs were 1.24 (CI, 0.90 to 1.70) and 0.74 (CI, 0.54 to 1.00), respectively (nominal P for interaction = 0.018). The sHR (bamlanivimab vs. placebo) was also more than 1 for those with plasma antigen or nasal viral RNA levels above median level at entry and was greatest for those without antibodies and with elevated levels of antigen (sHR, 1.48 [CI, 0.99 to 2.23]) or viral RNA (sHR, 1.89 [CI, 1.23 to 2.91]). Hazard ratios for the composite safety outcome (LIMITATION: Subgroup analysis of a trial prematurely stopped because of futility; small sample size; multiple subgroups analyzed.CONCLUSION: Efficacy and safety of bamlanivimab may differ depending on whether an endogenous nAb response has been mounted. The limited sample size of the study does not allow firm conclusions based on these findings, and further independent trials are required that assess other types of passive immune therapies in the same patient setting.PRIMARY FUNDING SOURCE: U.S. government Operation Warp Speed and National Institute of Allergy and Infectious Diseases.
اللغة: English
تدمد: 0003-4819
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c47486ea46158d87443ce42801dba2f
https://vbn.aau.dk/da/publications/c530ec33-9c51-477d-98fa-36df01391484
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....4c47486ea46158d87443ce42801dba2f
قاعدة البيانات: OpenAIRE