COVID-19 Immunologic Antiviral Therapy With Omalizumab (CIAO)—a Randomized Controlled Clinical Trial
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...
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creator | Le, Michelle Khoury, Lauren Lu, Yang Prosty, Connor Cormier, Maxime Cheng, Mathew P Fowler, Robert Murthy, Srinivas Tsang, Jennifer L Y Ben-Shoshan, Moshe Rahme, Elham Golchi, Shirin Dendukuri, Nandini Lee, Todd C Netchiporouk, Elena |
description | 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
In this, double-blind multicenter randomized phase II clinical trial, omalizumab had a 93% posterior probability at reducing COVID-19 mortality and/or mechanical ventilation at day 14, and a 75% probability at reducing all-cause mortality at day 28 regardless of the presence of atopy. Its use was safe in severely ill patients. This study supports the development of a phase III program to study the antiviral and anti-inflammatory effect of omalizumab in severe respiratory |
doi_str_mv | 10.1093/ofid/ofae102 |
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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
In this, double-blind multicenter randomized phase II clinical trial, omalizumab had a 93% posterior probability at reducing COVID-19 mortality and/or mechanical ventilation at day 14, and a 75% probability at reducing all-cause mortality at day 28 regardless of the presence of atopy. Its use was safe in severely ill patients. This study supports the development of a phase III program to study the antiviral and anti-inflammatory effect of omalizumab in severe respiratory viral illnesses.</description><identifier>ISSN: 2328-8957</identifier><identifier>EISSN: 2328-8957</identifier><identifier>DOI: 10.1093/ofid/ofae102</identifier><identifier>PMID: 38560604</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Acute respiratory distress syndrome ; Canada ; Clinical trials ; Clinical Trials and Therapeutics ; Coronaviruses ; Denosumab ; Health aspects ; Hospital patients ; Immunoglobulin E ; Mortality ; Omalizumab ; Pharmaceutical industry ; Quebec ; United States</subject><ispartof>Open Forum Infectious Diseases, 2024-04, Vol.11 (4), p.ofae102-ofae102</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. 2024</rights><rights>The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America.</rights><rights>COPYRIGHT 2024 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c441t-477f23d97291c99d3953d1fcfa4e53447097732080a62b58d075d59d2e3f96743</cites><orcidid>0000-0002-9393-0922 ; 0000-0001-6790-220X ; 0000-0002-9476-839X ; 0000-0002-4867-2063 ; 0000-0002-6692-7787 ; 0000-0002-2267-4239</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10977629/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10977629/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1598,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38560604$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Le, Michelle</creatorcontrib><creatorcontrib>Khoury, Lauren</creatorcontrib><creatorcontrib>Lu, Yang</creatorcontrib><creatorcontrib>Prosty, Connor</creatorcontrib><creatorcontrib>Cormier, Maxime</creatorcontrib><creatorcontrib>Cheng, Mathew P</creatorcontrib><creatorcontrib>Fowler, Robert</creatorcontrib><creatorcontrib>Murthy, Srinivas</creatorcontrib><creatorcontrib>Tsang, Jennifer L Y</creatorcontrib><creatorcontrib>Ben-Shoshan, Moshe</creatorcontrib><creatorcontrib>Rahme, Elham</creatorcontrib><creatorcontrib>Golchi, Shirin</creatorcontrib><creatorcontrib>Dendukuri, Nandini</creatorcontrib><creatorcontrib>Lee, Todd C</creatorcontrib><creatorcontrib>Netchiporouk, Elena</creatorcontrib><title>COVID-19 Immunologic Antiviral Therapy With Omalizumab (CIAO)—a Randomized Controlled Clinical Trial</title><title>Open Forum Infectious Diseases</title><addtitle>Open Forum Infect Dis</addtitle><description>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
In this, double-blind multicenter randomized phase II clinical trial, omalizumab had a 93% posterior probability at reducing COVID-19 mortality and/or mechanical ventilation at day 14, and a 75% probability at reducing all-cause mortality at day 28 regardless of the presence of atopy. Its use was safe in severely ill patients. This study supports the development of a phase III program to study the antiviral and anti-inflammatory effect of omalizumab in severe respiratory viral illnesses.</description><subject>Acute respiratory distress syndrome</subject><subject>Canada</subject><subject>Clinical trials</subject><subject>Clinical Trials and Therapeutics</subject><subject>Coronaviruses</subject><subject>Denosumab</subject><subject>Health aspects</subject><subject>Hospital patients</subject><subject>Immunoglobulin E</subject><subject>Mortality</subject><subject>Omalizumab</subject><subject>Pharmaceutical industry</subject><subject>Quebec</subject><subject>United States</subject><issn>2328-8957</issn><issn>2328-8957</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kctq3DAUhkVpacI0u66Ld00hTnWzZa3K4N4GAgMlbZdCo8uMii5T2Q4kqz5EnrBPUpmZhnRTBEeHo_98_OIH4CWClwhy8jZZp0uRBkH8BJxigru64w17-qg_AWfD8ANCiBBsIOPPwQnpmha2kJ4C26-_rd7XiFerEKaYfNo6VS3j6G5clr663pks97fVdzfuqnWQ3t1NQW6q8361XL_5_eteVl9k1Cm4O6OrPsUxJ-_n1rvo1EzITvoX4JmVfjBnx3sBvn78cN1_rq_Wn1b98qpWlKKxpoxZTDRnmCPFuSa8IRpZZSU1DaGUQc4YwbCDssWbptOQNbrhGhtiecsoWYB3B-5-2gSjlSl-pBf77ILMtyJJJ_59iW4ntulGoJncYl4I50dCTj8nM4wiuEEZ72U0aRoEgQQhQknxsQCXB-lWeiNctKkgVTnaBKdSNNaV-ZJxihgsnsvCxWFB5TQM2dgHYwjODoiY8xTHPIv81ePPPIj_plcErw-CNO3_j_oDQ1Cpug</recordid><startdate>20240401</startdate><enddate>20240401</enddate><creator>Le, Michelle</creator><creator>Khoury, Lauren</creator><creator>Lu, Yang</creator><creator>Prosty, Connor</creator><creator>Cormier, Maxime</creator><creator>Cheng, Mathew P</creator><creator>Fowler, Robert</creator><creator>Murthy, Srinivas</creator><creator>Tsang, Jennifer L Y</creator><creator>Ben-Shoshan, Moshe</creator><creator>Rahme, Elham</creator><creator>Golchi, Shirin</creator><creator>Dendukuri, Nandini</creator><creator>Lee, Todd C</creator><creator>Netchiporouk, Elena</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9393-0922</orcidid><orcidid>https://orcid.org/0000-0001-6790-220X</orcidid><orcidid>https://orcid.org/0000-0002-9476-839X</orcidid><orcidid>https://orcid.org/0000-0002-4867-2063</orcidid><orcidid>https://orcid.org/0000-0002-6692-7787</orcidid><orcidid>https://orcid.org/0000-0002-2267-4239</orcidid></search><sort><creationdate>20240401</creationdate><title>COVID-19 Immunologic Antiviral Therapy With Omalizumab (CIAO)—a Randomized Controlled Clinical Trial</title><author>Le, Michelle ; Khoury, Lauren ; Lu, Yang ; Prosty, Connor ; Cormier, Maxime ; Cheng, Mathew P ; Fowler, Robert ; Murthy, Srinivas ; Tsang, Jennifer L Y ; Ben-Shoshan, Moshe ; Rahme, Elham ; Golchi, Shirin ; Dendukuri, Nandini ; Lee, Todd C ; Netchiporouk, Elena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-477f23d97291c99d3953d1fcfa4e53447097732080a62b58d075d59d2e3f96743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acute respiratory distress syndrome</topic><topic>Canada</topic><topic>Clinical trials</topic><topic>Clinical Trials and Therapeutics</topic><topic>Coronaviruses</topic><topic>Denosumab</topic><topic>Health aspects</topic><topic>Hospital patients</topic><topic>Immunoglobulin E</topic><topic>Mortality</topic><topic>Omalizumab</topic><topic>Pharmaceutical industry</topic><topic>Quebec</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Le, Michelle</creatorcontrib><creatorcontrib>Khoury, Lauren</creatorcontrib><creatorcontrib>Lu, Yang</creatorcontrib><creatorcontrib>Prosty, Connor</creatorcontrib><creatorcontrib>Cormier, Maxime</creatorcontrib><creatorcontrib>Cheng, Mathew P</creatorcontrib><creatorcontrib>Fowler, Robert</creatorcontrib><creatorcontrib>Murthy, Srinivas</creatorcontrib><creatorcontrib>Tsang, Jennifer L Y</creatorcontrib><creatorcontrib>Ben-Shoshan, Moshe</creatorcontrib><creatorcontrib>Rahme, Elham</creatorcontrib><creatorcontrib>Golchi, Shirin</creatorcontrib><creatorcontrib>Dendukuri, Nandini</creatorcontrib><creatorcontrib>Lee, Todd C</creatorcontrib><creatorcontrib>Netchiporouk, Elena</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Open Forum Infectious Diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Le, Michelle</au><au>Khoury, Lauren</au><au>Lu, Yang</au><au>Prosty, Connor</au><au>Cormier, Maxime</au><au>Cheng, Mathew P</au><au>Fowler, Robert</au><au>Murthy, Srinivas</au><au>Tsang, Jennifer L Y</au><au>Ben-Shoshan, Moshe</au><au>Rahme, Elham</au><au>Golchi, Shirin</au><au>Dendukuri, Nandini</au><au>Lee, Todd C</au><au>Netchiporouk, Elena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>COVID-19 Immunologic Antiviral Therapy With Omalizumab (CIAO)—a Randomized Controlled Clinical Trial</atitle><jtitle>Open Forum Infectious Diseases</jtitle><addtitle>Open Forum Infect Dis</addtitle><date>2024-04-01</date><risdate>2024</risdate><volume>11</volume><issue>4</issue><spage>ofae102</spage><epage>ofae102</epage><pages>ofae102-ofae102</pages><issn>2328-8957</issn><eissn>2328-8957</eissn><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
In this, double-blind multicenter randomized phase II clinical trial, omalizumab had a 93% posterior probability at reducing COVID-19 mortality and/or mechanical ventilation at day 14, and a 75% probability at reducing all-cause mortality at day 28 regardless of the presence of atopy. Its use was safe in severely ill patients. This study supports the development of a phase III program to study the antiviral and anti-inflammatory effect of omalizumab in severe respiratory viral illnesses.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>38560604</pmid><doi>10.1093/ofid/ofae102</doi><orcidid>https://orcid.org/0000-0002-9393-0922</orcidid><orcidid>https://orcid.org/0000-0001-6790-220X</orcidid><orcidid>https://orcid.org/0000-0002-9476-839X</orcidid><orcidid>https://orcid.org/0000-0002-4867-2063</orcidid><orcidid>https://orcid.org/0000-0002-6692-7787</orcidid><orcidid>https://orcid.org/0000-0002-2267-4239</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acute respiratory distress syndrome Canada Clinical trials Clinical Trials and Therapeutics Coronaviruses Denosumab Health aspects Hospital patients Immunoglobulin E Mortality Omalizumab Pharmaceutical industry Quebec United States |
title | COVID-19 Immunologic Antiviral Therapy With Omalizumab (CIAO)—a Randomized Controlled Clinical Trial |
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