학술논문

Report of the first seven agents in the I-SPY COVID trial: a phase 2, open label, adaptive platform randomised controlled trial
Document Type
article
Author
Consortium, The I-SPY COVIDFiles, D ClarkAggarwal, NeilAlbertson, TimothyAuld, SaraBeitler, Jeremy RBerger, PaulBurnham, Ellen LCalfee, Carolyn SCobb, NathanCrippa, AlessioDiscacciati, AndreaEklund, MartinEsserman, LauraFriedman, EliotGandotra, SheetalKhan, KashifKoff, JonathanKumar, SanthiLiu, Kathleen DMartin, Thomas RMatthay, Michael AMeyer, Nuala JObermiller, TimothyRobinson, PhilipRussell, DerekThomas, KarlWong, FumWunderink, Richard GWurfel, Mark MYen, AlbertYoussef, Fady ADarmanian, AnitaDzierba, Amy LGarcia, IvanGosek, KatarzynaMadahar, PurnemaMittel, Aaron MMuir, JustinRosen, AmandaSchicchi, JohnSerra, Alexis LWahab, RominaGibbs, Kevin WLandreth, LeighaLaRose, MaryParks, LisaWynn, AdinaIttner, Caroline AGMangalmurti, Nilman SReilly, John PHarris, DonnaMethukupally, AbhishekPatel, SiddharthBoerger, LindsieKazianis, JohnHiggins, CarrieMcKeehan, JeffDaniel, BrianFields, ScottHurst-Hopf, JamesJauregui, AlejandraSwigart, Lamorna BrownBlevins, DanielNguyen, CatherineSuarez, AlexisTanios, Maged ASarafian, FarjadShah, UsmanAdelman, MaxCreel-Bulos, ChristinaDetelich, JoshuaHarris, GavinNugent, KatherineSpainhour, ChristinaYang, PhilipHaczku, AngelaHardy, ErinHarper, RichartMorrissey, BrianSandrock, ChristianBudinger, GR ScottDonnelly, Helen KSinger, Benjamin DMoskowitz, AriColeman, MelissaLevitt, JosephLu, RuixiaoHenderson, PaulAsare, AdamDunn, ImogeneBarragan, Alejandro Botello
Source
Subject
Health Services
Clinical Trials and Supportive Activities
Clinical Research
Good Health and Well Being
I-SPY COVID Consortium
Acute lung injury
Clinical trial
Respiratory insufficiency
SARS-CoV-2
Language
Abstract
BackgroundAn urgent need exists to rapidly screen potential therapeutics for severe COVID-19 or other emerging pathogens associated with high morbidity and mortality.MethodsUsing an adaptive platform design created to rapidly evaluate investigational agents, hospitalised patients with severe COVID-19 requiring ≥6 L/min oxygen were randomised to either a backbone regimen of dexamethasone and remdesivir alone (controls) or backbone plus one open-label investigational agent. Patients were enrolled to the arms described between July 30, 2020 and June 11, 2021 in 20 medical centres in the United States. The platform contained up to four potentially available investigational agents and controls available for randomisation during a single time-period. The two primary endpoints were time-to-recovery (