COVID-19 Immunologic Antiviral Therapy With Omalizumab (CIAO)—a Randomized Controlled Clinical Trial

Author:

Le Michelle1ORCID,Khoury Lauren2,Lu Yang3,Prosty Connor2ORCID,Cormier Maxime4,Cheng Mathew P5ORCID,Fowler Robert6,Murthy Srinivas7ORCID,Tsang Jennifer L Y8,Ben-Shoshan Moshe9,Rahme Elham3,Golchi Shirin3,Dendukuri Nandini3,Lee Todd C5ORCID,Netchiporouk Elena1ORCID

Affiliation:

1. Division of Dermatology, Department of Medicine, McGill University , Montreal, QC , Canada

2. Faculty of Medicine, McGill University , Montreal, QC , Canada

3. Department of Epidemiology, Biostatistics, and Occupational Health, McGill University , Montreal, QC , Canada

4. Division of Respiratory Medicine, Department of Medicine, McGill University , Montreal, QC , Canada

5. Divisions of Infectious Diseases & Medical Microbiology, McGill University , McGill's Interdisciplinary Initiative in Infection and Immunity, Montreal, QC, Canada

6. Department of Critical Care Medicine, Sunnybrook Health Sciences Centre , Toronto, ON , Canada

7. Department of Pediatrics, Faculty of Medicine, University of British Columbia , Vancouver, BC , Canada

8. Niagara Health Knowledge Institute, Niagara Health, St. Catharines, ON , Canada

9. Division of Allergy, Immunology and Dermatology, Department of Pediatrics, McGill University , Montreal, QC , Canada

Abstract

Abstract Background Omalizumab is an anti-immunoglobulin E monoclonal antibody used to treat moderate to severe chronic idiopathic urticaria, asthma, and nasal polyps. Recent research suggested that omalizumab may enhance the innate antiviral response and have anti-inflammatory properties. Objective We aimed to investigate the efficacy and safety of omalizumab in adults hospitalized for coronavirus disease 2019 (COVID-19) pneumonia. Methods This was a phase II randomized, double blind, placebo-controlled trial comparing omalizumab with placebo (in addition to standard of care) in hospitalized patients with COVID-19. The primary endpoint was the composite of mechanical ventilation and/or death at day 14. Secondary endpoints included all-cause mortality at day 28, time to clinical improvement, and duration of hospitalization. Results Of 41 patients recruited, 40 were randomized (20 received the study drug and 20 placebo). The median age of the patients was 74 years and 55.0% were male. Omalizumab was associated with a 92.6% posterior probability of a reduction in mechanical ventilation and death on day 14 with an adjusted odds ratio of 0.11 (95% credible interval 0.002-2.05). Omalizumab was also associated with a 75.9% posterior probability of reduced all-cause mortality on day 28 with an adjusted odds ratio of 0.49 (95% credible interval, 0.06-3.90). No statistically significant differences were found for the time to clinical improvement and duration of hospitalization. Numerically fewer adverse events were reported in the omalizumab group and there were no drug-related serious adverse events. Conclusions These results suggest that omalizumab could prove protective against death and mechanical ventilation in hospitalized patients with COVID-19. This study could also support the development of a phase III trial program investigating the antiviral and anti-inflammatory effect of omalizumab for severe respiratory viral illnesses requiring hospital admission. ClinicalTrials.gov ID: NCT04720612

Funder

Ministre de l’Économie et Innovation

Fonds de Recherche Santé Québec

MUHC Foundation

Novartis Pharmaceuticals Corporation

Publisher

Oxford University Press (OUP)

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