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Fostamatinib for Hospitalized Adults With COVID-19 and Hypoxemia: A Randomized Clinical Trial.

Authors :
Collins SP
Shotwell MS
Strich JR
Gibbs KW
de Wit M
Files DC
Harkins M
Hudock K
Merck LH
Moskowitz A
Apodaca KD
Barksdale A
Safdar B
Javaheri A
Sturek JM
Schrager H
Iovine NM
Tiffany B
Douglas I
Levitt J
Ginde AA
Hager DN
Shapiro N
Duggal A
Khan A
Lanspa M
Chen P
Gentile N
Harris E
Gong M
Sellers S
Goodwin AJ
Tidswell MA
Filbin M
Desai N
Gutiérrez F
Estrada V
Burgos J
Boyles T
Paño-Pardo JR
Hussen N
Rosenberg Y
Troendle J
Bernard GR
Bistran-Hall AJ
Walsh K
Casey JD
DeClercq J
Joly MM
Pulley J
Rice TW
Schildcrout JS
Wang L
Semler MW
Self WH
Source :
JAMA network open [JAMA Netw Open] 2024 Dec 02; Vol. 7 (12), pp. e2448215. Date of Electronic Publication: 2024 Dec 02.
Publication Year :
2024

Abstract

Importance: Fostamatinib, a spleen tyrosine kinase inhibitor, has been reported to improve outcomes of COVID-19.<br />Objective: To evaluate the efficacy and safety of fostamatinib in adults hospitalized with COVID-19 and hypoxemia.<br />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.<br />Interventions: Fostamatinib, 150 mg orally twice daily for 14 days, or placebo.<br />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.<br />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.<br />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.<br />Trial Registration: ClinicalTrials.gov Identifier: NCT04924660.

Details

Language :
English
ISSN :
2574-3805
Volume :
7
Issue :
12
Database :
MEDLINE
Journal :
JAMA network open
Publication Type :
Academic Journal
Accession number :
39625722
Full Text :
https://doi.org/10.1001/jamanetworkopen.2024.48215