Angiotensin receptor blockers for the treatment of covid-19: pragmatic, adaptive, multicentre, phase 3, randomised controlled trial

Meg J Jardine, Sradha S Kotwal, Abhinav Bassi, Carinna Hockham, Mark Jones, Arlen Wilcox, Carol Pollock, Louise M Burrell, James McGree, Vinay Rathore, Christine R Jenkins, Lalit Gupta, Angus Ritchie, Ashpak Bangi, Sanjay D'Cruz, Andrew J McLachlan, Simon Finfer, Michelle M Cummins, Thomas Snelling, Vivekanand Jha, CLARITY trial investigators, Ashish Bhalla, Gregory Fox, Santosh Kumar Nag, Angela Makris, George Mangos, Jeffrey Post, Indu Ramachandra Rao, Louisa Sukkar, Richard Sullivan, Gian Luca Di Tanna, Jason Trubiano, Sophia Zoungas, Lovenish Bains, Atul Jindal, Nitin M Nagarkar, Saurabh Nayak, Meg J Jardine, Sradha S Kotwal, Abhinav Bassi, Carinna Hockham, Mark Jones, Arlen Wilcox, Carol Pollock, Louise M Burrell, James McGree, Vinay Rathore, Christine R Jenkins, Lalit Gupta, Angus Ritchie, Ashpak Bangi, Sanjay D'Cruz, Andrew J McLachlan, Simon Finfer, Michelle M Cummins, Thomas Snelling, Vivekanand Jha, CLARITY trial investigators, Ashish Bhalla, Gregory Fox, Santosh Kumar Nag, Angela Makris, George Mangos, Jeffrey Post, Indu Ramachandra Rao, Louisa Sukkar, Richard Sullivan, Gian Luca Di Tanna, Jason Trubiano, Sophia Zoungas, Lovenish Bains, Atul Jindal, Nitin M Nagarkar, Saurabh Nayak

Abstract

Objective: To determine whether disrupting the renin angiotensin system with angiotensin receptor blockers will improve clinical outcomes in people with covid-19.

Design: CLARITY was a pragmatic, adaptive, multicentre, phase 3, randomised controlled trial.

Setting: 17 hospital sites in India and Australia.

Participants: Participants were at least 18 years old, previously untreated with angiotensin receptor blockers, with a laboratory confirmed diagnosis of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection who had been admitted to hospital for management of covid-19.

Intervention: Oral angiotensin receptor blockers (telmisartan in India) or placebo (1:1) for 28 days.

Main outcome measures: The primary endpoint was covid-19 disease severity using a modified World Health Organization Clinical Progression Scale (WHO scale) at day 14. Secondary outcomes were WHO scale scores at day 28, mortality, intensive care unit admission, and respiratory failure. Analyses were evaluated on an ordinal scale in the intention-to-treat population.

Results: Between 3 May 2020 and 13 November 2021, 2930 people were screened for eligibility, with 393 randomly assigned to angiotensin receptor blockers (of which 388 (98.7%) to telmisartan 40 mg/day) and 394 to the control group. 787 participants were randomised: 778 (98.9%) from India and nine (1.1%) from Australia. The median WHO scale score at day 14 was 1 (interquartile range 1-1) in 384 participants assigned angiotensin receptor blockers and 1 (1-1) in 382 participants assigned placebo (adjusted odds ratio 1.51 (95% credible interval 1.02 to 2.23), probability of an odds ratio of >1 (Pr(OR>1)=0.98). WHO scale scores at day 28 showed little evidence of difference between groups (1.02 (0.55 to 1.87), Pr(OR>1)=0.53). The trial was stopped when a prespecified futility rule was met.

Conclusions: In patients admitted to hospital for covid-19, mostly with mild disease, not requiring oxygen, no evidence of benefit, based on disease severity score, was found for treatment with angiotensin receptor blockers, using predominantly 40 mg/day of telmisartan.

Trial registration: ClinicalTrials.gov NCT04394117.

Conflict of interest statement

Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/disclosure-of-interest/ and declare: support from the Australian government and the University of Sydney for the submitted work; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years except the following: MJ is responsible for research projects that have received funding from Amgen, Baxter, CSL, Dimerix, Eli Lilly, Gambro, and Merck Sharp and Dohme; has received advisory, steering committee or speaker fees, or both, from Akebia, Amgen, Astra Zeneca, Baxter, Bayer, Boehringer Ingelheim, Cesas Linx, Chinook, CSL, Janssen, Medscape, Merck Sharp Dohme, Roche, and Vifor; CP serves on advisory boards for AstraZeneca, Boehringer Ingelheim, Merck Sharp and Dohme, and Novartis; CJ serves on advisory boards for AstraZeneca, Boehringer Ingelheim, Chiesi, GlaxoSmithKline, Novartis, and Sanofi-Genzyme; VJ has received grants from Baxter Healthcare, Biocon, and GlaxoSmithKline, and speaker fees or on the advisory board for AstraZeneca, Baxter Healthcare, NephroPlus, Sanofi; no other relationships or activities that could appear to have influenced the submitted work.

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. No commercial re-use. See rights and permissions. Published by BMJ.

Figures

Fig 1
Fig 1
Participant flow in the CLARITY trial. eGFR=estimated glomerular filtration rate. SOC=standard of care. ARB=angiotensin receptor blocker. *Four did not receive allocated intervention
Fig 2
Fig 2
Bar graph showing WHO progression scale of covid-19 severity between study groups. ARB=angiotensin receptor blocker
Fig 3
Fig 3
Line graph showing WHO progression scale of covid-19 severity between study groups. ARB=angiotensin receptor blocker

References

    1. Hoffmann M, Kleine-Weber H, Schroeder S, Kruger N, Herrler T, Erichsen S, et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell 2020;181:271-80.e8.
    1. Lan J, Ge J, Yu J, et al. . Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor. Nature 2020;581:215-20. 10.1038/s41586-020-2180-5
    1. Parasher A. COVID-19: Current understanding of its pathophysiology, clinical presentation and treatment. Postgrad Med J 2020:postgradmedj-2020-138577.
    1. Yeung ML, Teng JLL, Jia L, et al. . Soluble ACE2-mediated cell entry of SARS-CoV-2 via interaction with proteins related to the renin-angiotensin system. Cell 2021;184:2212-2228.e12. 10.1016/j.cell.2021.02.053
    1. Kuba K, Imai Y, Rao S, et al. . A crucial role of angiotensin converting enzyme 2 (ACE2) in SARS coronavirus-induced lung injury. Nat Med 2005;11:875-9. 10.1038/nm1267
    1. Imai Y, Kuba K, Rao S, et al. . Angiotensin-converting enzyme 2 protects from severe acute lung failure. Nature 2005;436:112-6. 10.1038/nature03712
    1. Hockham C, Kotwal S, Wilcox A, et al. CLARITY Investigators . Protocol for the Controlled evaLuation of Angiotensin Receptor blockers for COVID-19 respIraTorY disease (CLARITY): a randomised controlled trial. Trials 2021;22:573. 10.1186/s13063-021-05521-0
    1. McGree JM, Hockham C, Kotwal S, et al. CLARITY Trial Steering Committee . Controlled evaLuation of Angiotensin Receptor Blockers for COVID-19 respIraTorY disease (CLARITY): statistical analysis plan for a randomised controlled Bayesian adaptive sample size trial. Trials 2022;23:361. 10.1186/s13063-022-06167-2
    1. WHO Working Group on the Clinical Characterisation and Management of COVID-19 infection . Group on the clinical characterisation and management of covid-19 infection. A minimal common outcome measure set for covid-19 clinical research. Lancet Infect Dis 2020;20:e192-7 10.1016/S1473-3099(20)30483-7.
    1. Cao B, Wang Y, Wen D, et al. . A trial of lopinavir-ritonavir in adults hospitalized with severe covid-19. N Engl J Med 2020;382:1787-99. 10.1056/NEJMoa2001282
    1. Ad-hoc working group of ERBP. Fliser DLaville MCovic A, et al. A European Renal Best Practice (ERBP) position statement on the Kidney Disease Improving Global Outcomes (KDIGO) clinical practice guidelines on acute kidney injury: part 1: definitions, conservative management and contrast-induced nephropathy. Nephrol Dial Transplant 2012;27:4263-72.
    1. Docherty AB, Harrison EM, Green CA, et al. ISARIC4C investigators . Features of 20 133 UK patients in hospital with covid-19 using the ISARIC WHO Clinical Characterisation Protocol: prospective observational cohort study. BMJ 2020;369:m1985. 10.1136/bmj.m1985
    1. International Severe Acute Respiratory and Emerging Infections Consortium (ISARIC). COVID-19 report: 19 May 2020. 2020.
    1. Marschner IC. Estimating age-specific COVID-19 fatality risk and time to death by comparing population diagnosis and death patterns: Australian data. BMC Med Res Methodol 2021;21:126. 10.1186/s12874-021-01314-w
    1. Mathur R, Rentsch CT, Morton CE, et al. OpenSAFELY Collaborative . Ethnic differences in SARS-CoV-2 infection and COVID-19-related hospitalisation, intensive care unit admission, and death in 17 million adults in England: an observational cohort study using the OpenSAFELY platform. Lancet 2021;397:1711-24. 10.1016/S0140-6736(21)00634-6
    1. Horby P, Lim WS, Emberson JR, et al. RECOVERY Collaborative Group . Dexamethasone in Hospitalized Patients with Covid-19. N Engl J Med 2021;384:693-704. 10.1056/NEJMoa2021436
    1. Ritchie H, Ortiz-Ospina E, Beltekian D, et al. Coronavirus (COVID-19) Cases 2022. .
    1. Bauer A, Schreinlechner M, Sappler N, et al. ACEI-COVID investigators . Discontinuation versus continuation of renin-angiotensin-system inhibitors in COVID-19 (ACEI-COVID): a prospective, parallel group, randomised, controlled, open-label trial. Lancet Respir Med 2021;9:863-72. 10.1016/S2213-2600(21)00214-9
    1. Cohen JB, Hanff TC, William P, et al. . Continuation versus discontinuation of renin-angiotensin system inhibitors in patients admitted to hospital with COVID-19: a prospective, randomised, open-label trial. Lancet Respir Med 2021;9:275-84. 10.1016/S2213-2600(20)30558-0
    1. REMAP-CAP. A randomised, embedded, multi-factorial, adaptive platform trial for community-acquired pneumonia. .
    1. Duarte M, Pelorosso F, Nicolosi LN, et al. . Telmisartan for treatment of Covid-19 patients: An open multicenter randomized clinical trial. EClinicalMedicine 2021;37:100962. 10.1016/j.eclinm.2021.100962
    1. Geriak M, Haddad F, Kullar R, et al. . Randomized prospective open label study shows no impact on clinical outcome of adding losartan to hospitalized covid-19 patients with mild hypoxemia. Infect Dis Ther 2021;10:1323-30. 10.1007/s40121-021-00453-3
    1. Nouri-Vaskeh M, Kalami N, Zand R, et al. . Comparison of losartan and amlodipine effects on the outcomes of patient with COVID-19 and primary hypertension: A randomised clinical trial. Int J Clin Pract 2021;75:e14124. 10.1111/ijcp.14124
    1. Puskarich MA, Cummins NW, Ingraham NE, et al. . A multi-center phase II randomized clinical trial of losartan on symptomatic outpatients with COVID-19. EClinicalMedicine 2021;37:100957. 10.1016/j.eclinm.2021.100957
    1. Puskarich MA, Ingraham NE, Merck LH, et al. Angiotensin Receptor Blocker Based Lung Protective Strategies for Inpatients With COVID-19 (ALPS-IP) Investigators . Efficacy of losartan in hospitalized patients with covid-19-induced lung injury: a randomized clinical trial. JAMA Netw Open 2022;5:e222735. 10.1001/jamanetworkopen.2022.2735
    1. Lopes RD, Macedo AVS, de Barros E Silva PGM, et al. BRACE CORONA Investigators . Effect of discontinuing vs continuing angiotensin-converting enzyme inhibitors and angiotensin ii receptor blockers on days alive and out of the hospital in patients admitted with covid-19: a randomized clinical trial. JAMA 2021;325:254-64. 10.1001/jama.2020.25864
    1. Sharma A, Elharram M, Afilalo J, et al. . A randomized controlled trial of renin-angiotensin-aldosterone system inhibitor management in patients admitted in hospital with COVID-19. Am Heart J 2022;247:76-89. 10.1016/j.ahj.2022.01.015

Source: PubMed

3
订阅