Phillip D Monk
Safety and efficacy of inhaled nebulised interferon beta-1a (SNG001) for treatment of SARS-CoV-2 infection: a randomised, double-blind, placebo-controlled, phase 2 trial
Monk, Phillip D; Marsden, Richard J; Tear, Victoria J; Brookes, Jody; Batten, Toby N; Mankowski, Marcin; Gabbay, Felicity J; Davies, Donna E; Holgate, Stephen T; Ho, Ling Pei; Clark, Tristan; Djukanovic, Ratko; Wilkinson, Tom M A; Crooks, Michael G.; Dosanjh, Davinder PS; Siddiqui, Salman; Rahman, Najib M; Smith, Jacklyn A; Horsley, Alexander; Harrison, Timothy W; Saralaya, Dinesh; McGarvey, Lorcan; Watson, Alastair; Foster, Edmund; Fleet, Adam; Singh, Dave; Hemmings, Sophie; Aitken, Sandra; Dudley, Sarah; Beegan, Rona; Thompson, Angela; Rodrigues, Pedro MB
Authors
Richard J Marsden
Victoria J Tear
Jody Brookes
Toby N Batten
Marcin Mankowski
Felicity J Gabbay
Donna E Davies
Stephen T Holgate
Ling Pei Ho
Tristan Clark
Ratko Djukanovic
Tom M A Wilkinson
Prof Michael Crooks m.g.crooks@hull.ac.uk
Professor of Respiratory Medicine
Davinder PS Dosanjh
Salman Siddiqui
Najib M Rahman
Jacklyn A Smith
Alexander Horsley
Timothy W Harrison
Dinesh Saralaya
Lorcan McGarvey
Alastair Watson
Edmund Foster
Adam Fleet
Dave Singh
Sophie Hemmings
Sandra Aitken
Sarah Dudley
Rona Beegan
Angela Thompson
Pedro MB Rodrigues
Abstract
Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection carries a substantial risk of severe and prolonged illness; treatment options are currently limited. We assessed the efficacy and safety of inhaled nebulised interferon beta-1a (SNG001) for the treatment of patients admitted to hospital with COVID-19. Methods: We did a randomised, double-blind, placebo-controlled, phase 2 pilot trial at nine UK sites. Adults aged 18 years or older and admitted to hospital with COVID-19 symptoms, with a positive RT-PCR or point-of-care test, or both, were randomly assigned (1:1) to receive SNG001 (6 MIU) or placebo by inhalation via a mouthpiece daily for 14 days. The primary outcome was the change in clinical condition on the WHO Ordinal Scale for Clinical Improvement (OSCI) during the dosing period in the intention-to-treat population (all randomised patients who received at least one dose of the study drug). The OSCI is a 9-point scale, where 0 corresponds to no infection and 8 corresponds to death. Multiple analyses were done to identify the most suitable statistical method for future clinical trials. Safety was assessed by monitoring adverse events for 28 days. This trial is registered with Clinicaltrialsregister.eu (2020-001023-14) and ClinicalTrials.gov (NCT04385095); the pilot trial of inpatients with COVID-19 is now completed. Findings: Between March 30 and May 30, 2020, 101 patients were randomly assigned to SNG001 (n=50) or placebo (n=51). 48 received SNG001 and 50 received placebo and were included in the intention-to-treat population. 66 (67%) patients required oxygen supplementation at baseline: 29 in the placebo group and 37 in the SNG001 group. Patients receiving SNG001 had greater odds of improvement on the OSCI scale (odds ratio 2·32 [95% CI 1·07–5·04]; p=0·033) on day 15 or 16 and were more likely than those receiving placebo to recover to an OSCI score of 1 (no limitation of activities) during treatment (hazard ratio 2·19 [95% CI 1·03–4·69]; p=0·043). SNG001 was well tolerated. The most frequently reported treatment-emergent adverse event was headache (seven [15%] patients in the SNG001 group and five [10%] in the placebo group). There were three deaths in the placebo group and none in the SNG001 group. Interpretation: Patients who received SNG001 had greater odds of improvement and recovered more rapidly from SARS-CoV-2 infection than patients who received placebo, providing a strong rationale for further trials. Funding: Synairgen Research.
Citation
Monk, P. D., Marsden, R. J., Tear, V. J., Brookes, J., Batten, T. N., Mankowski, M., Gabbay, F. J., Davies, D. E., Holgate, S. T., Ho, L. P., Clark, T., Djukanovic, R., Wilkinson, T. M. A., Crooks, M. G., Dosanjh, D. P., Siddiqui, S., Rahman, N. M., Smith, J. A., Horsley, A., Harrison, T. W., …Rodrigues, P. M. (2021). Safety and efficacy of inhaled nebulised interferon beta-1a (SNG001) for treatment of SARS-CoV-2 infection: a randomised, double-blind, placebo-controlled, phase 2 trial. The lancet. Respiratory medicine, 9(2), 196-206. https://doi.org/10.1016/S2213-2600%2820%2930511-7
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 12, 2020 |
Online Publication Date | Nov 12, 2020 |
Publication Date | 2021-02 |
Deposit Date | Feb 12, 2021 |
Publicly Available Date | May 13, 2021 |
Journal | The Lancet Respiratory Medicine |
Print ISSN | 2213-2600 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 9 |
Issue | 2 |
Pages | 196-206 |
DOI | https://doi.org/10.1016/S2213-2600%2820%2930511-7 |
Keywords | Pulmonary and Respiratory Medicine; SARS-CoV-2; Interferon beta-1a |
Public URL | https://hull-repository.worktribe.com/output/3660896 |
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Copyright Statement
©2020. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
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