TY - JOUR
T1 - Fostamatinib for Hospitalized Adults With COVID-19 and Hypoxemia
T2 - A Randomized Clinical Trial
AU - ACTIV-4 Host Tissue Investigators
AU - Collins, Sean P.
AU - Shotwell, Matthew S.
AU - Strich, Jeffrey R.
AU - Gibbs, Kevin W.
AU - de Wit, Marjolein
AU - Files, D. Clark
AU - Harkins, Michelle
AU - Hudock, Kris
AU - Merck, Lisa H.
AU - Moskowitz, Ari
AU - Apodaca, Krystle D.
AU - Barksdale, Aaron
AU - Safdar, Basmah
AU - Javaheri, Ali
AU - Sturek, Jeffrey M.
AU - Schrager, Harry
AU - Iovine, Nicole M.
AU - Tiffany, Brian
AU - Douglas, Ivor
AU - Levitt, Joseph
AU - Ginde, Adit A.
AU - Hager, David N.
AU - Shapiro, Nathan
AU - Duggal, Abhijit
AU - Khan, Akram
AU - Lanspa, Michael
AU - Chen, Peter
AU - Gentile, Nina
AU - Harris, Estelle
AU - Gong, Michelle
AU - Sellers, Subhashini
AU - Goodwin, Andrew J.
AU - Tidswell, Mark A.
AU - Filbin, Michael
AU - Desai, Neeraj
AU - Gutiérrez, Felix
AU - Estrada, Vicente
AU - Burgos, Joaquin
AU - Boyles, Tom
AU - Paño-Pardo, Jose R.
AU - Hussen, Nazreen
AU - Rosenberg, Yves
AU - Troendle, James
AU - Bernard, Gordon R.
AU - Bistran-Hall, Amanda J.
AU - Walsh, Kelly
AU - Casey, Jonathan D.
AU - DeClercq, Josh
AU - Joly, Meghan Morrison
AU - Pulley, Jill
AU - Rice, Todd W.
AU - Schildcrout, Jonathan S.
AU - Wang, Li
AU - Semler, Matthew W.
AU - Self, Wesley H.
PY - 2024/12/2
Y1 - 2024/12/2
N2 - Importance: Fostamatinib, a spleen tyrosine kinase inhibitor, has been reported to improve outcomes of COVID-19. Objective: To evaluate the efficacy and safety of fostamatinib in adults hospitalized with COVID-19 and hypoxemia. Design, Setting, and Participants: This multicenter, phase 3, placebo-controlled, double-blinded randomized clinical trial was conducted at 41 US sites and 21 international sites between November 17, 2021, and September 27, 2023; the last follow-up visit was December 31, 2023. Participants were adults aged 18 years or older hospitalized with acute SARS-CoV-2 infection and hypoxemia. Data were analyzed between January 10 and March 8, 2024. Interventions: Fostamatinib, 150 mg orally twice daily for 14 days, or placebo. Main Outcomes and Measures: The primary outcome was oxygen-free days, an ordinal outcome classifying a participant's status at day 28 based on mortality and duration of supplemental oxygen use. An adjusted odds ratio (AOR) greater than 1.0 was considered to indicate superiority of fostamatinib over placebo. A key secondary outcome was 28-day all-cause mortality. Safety outcomes included elevated transaminase values, neutropenia, and hypertension. Results: Of the 400 participants randomized (median age, 67 years [IQR, 58-76 years]; 210 [52.5%] men), 199 received fostamatinib and 201 received placebo. The mean (SD) number of oxygen-free days was 13.4 (12.4) in the fostamatinib group and 14.2 (12.1) in the placebo group (unadjusted mean difference, -1.26 days [95% CI, -3.52 to 1.00 days]; AOR, 0.82 [95% credible interval (CrI), 0.58-1.17]). Mortality at 28 days occurred in 22 of 195 patients (11.3%) in the fostamatinib group and 16 of 197 (8.1%) in the placebo group (AOR, 1.44; 95% CrI, 0.72-2.90). Aspartate aminotransferase elevation occurred more commonly in the fostamatinib group (23 [11.6%]) than in the placebo group (11 [5.5%]; AOR, 2.28; 95% CrI, 1.07-4.84). Other safety outcomes were similar between groups. Conclusions and Relevance: In this randomized clinical trial of adults hospitalized with COVID-19 and hypoxemia, fostamatinib did not increase the number of oxygen-free days compared with placebo. These results do not support the hypothesis that fostamatinib improves outcomes among adults hospitalized with hypoxemia during the Omicron era. Trial Registration: ClinicalTrials.gov Identifier: NCT04924660.
AB - Importance: Fostamatinib, a spleen tyrosine kinase inhibitor, has been reported to improve outcomes of COVID-19. Objective: To evaluate the efficacy and safety of fostamatinib in adults hospitalized with COVID-19 and hypoxemia. Design, Setting, and Participants: This multicenter, phase 3, placebo-controlled, double-blinded randomized clinical trial was conducted at 41 US sites and 21 international sites between November 17, 2021, and September 27, 2023; the last follow-up visit was December 31, 2023. Participants were adults aged 18 years or older hospitalized with acute SARS-CoV-2 infection and hypoxemia. Data were analyzed between January 10 and March 8, 2024. Interventions: Fostamatinib, 150 mg orally twice daily for 14 days, or placebo. Main Outcomes and Measures: The primary outcome was oxygen-free days, an ordinal outcome classifying a participant's status at day 28 based on mortality and duration of supplemental oxygen use. An adjusted odds ratio (AOR) greater than 1.0 was considered to indicate superiority of fostamatinib over placebo. A key secondary outcome was 28-day all-cause mortality. Safety outcomes included elevated transaminase values, neutropenia, and hypertension. Results: Of the 400 participants randomized (median age, 67 years [IQR, 58-76 years]; 210 [52.5%] men), 199 received fostamatinib and 201 received placebo. The mean (SD) number of oxygen-free days was 13.4 (12.4) in the fostamatinib group and 14.2 (12.1) in the placebo group (unadjusted mean difference, -1.26 days [95% CI, -3.52 to 1.00 days]; AOR, 0.82 [95% credible interval (CrI), 0.58-1.17]). Mortality at 28 days occurred in 22 of 195 patients (11.3%) in the fostamatinib group and 16 of 197 (8.1%) in the placebo group (AOR, 1.44; 95% CrI, 0.72-2.90). Aspartate aminotransferase elevation occurred more commonly in the fostamatinib group (23 [11.6%]) than in the placebo group (11 [5.5%]; AOR, 2.28; 95% CrI, 1.07-4.84). Other safety outcomes were similar between groups. Conclusions and Relevance: In this randomized clinical trial of adults hospitalized with COVID-19 and hypoxemia, fostamatinib did not increase the number of oxygen-free days compared with placebo. These results do not support the hypothesis that fostamatinib improves outcomes among adults hospitalized with hypoxemia during the Omicron era. Trial Registration: ClinicalTrials.gov Identifier: NCT04924660.
UR - http://www.scopus.com/inward/record.url?scp=85211395601&partnerID=8YFLogxK
U2 - 10.1001/jamanetworkopen.2024.48215
DO - 10.1001/jamanetworkopen.2024.48215
M3 - Article
C2 - 39625722
AN - SCOPUS:85211395601
SN - 2574-3805
VL - 7
SP - e2448215
JO - JAMA Network Open
JF - JAMA Network Open
IS - 12
ER -