tetano
Editor, Senior Moderator
Clin Med Insights Circ Respir Pulm Med
. 2022 Aug 10;16:11795484221119316.
doi: 10.1177/11795484221119316. eCollection 2022.
Efficacy and Safety of LY3127804, an Anti-Angiopoietin-2 Antibody, in a Randomized, Double-Blind, Placebo-Controlled Clinical Trial in Patients Hospitalized with Pneumonia and Presumed or Confirmed COVID-19
Rosie S Jones[SUP] 1 [/SUP], Patricia S Smith[SUP] 1 [/SUP], Paul H Berg[SUP] 1 [/SUP], Amparo de la Peña[SUP] 1 [/SUP], Paul P Cook[SUP] 2 [/SUP], Imad Shawa[SUP] 3 [/SUP], Kathleen M Kioussopoulos[SUP] 3 [/SUP], Yu Hu[SUP] 1 [/SUP], Robert J Schott[SUP] 1 [/SUP]
Affiliations
Abstract
Background: Severe cases of coronavirus disease 2019 (COVID-19) are characterized by progressive respiratory failure and the development of acute respiratory distress syndrome (ARDS), with high mortality rates for patients requiring mechanical ventilation. Levels of the vascular growth factor Angiopoietin 2 (Ang2) in plasma have been strongly correlated with increased ARDS risk in patients with pneumonia or sepsis. The intent of this study was to determine whether LY3127804, an anti-Ang2 monoclonal antibody, could reduce the need for mechanical ventilation among patients admitted to the hospital with pneumonia and presumed or confirmed COVID-19.
Methods: Patients admitted to hospital with confirmed pneumonia, presumed or confirmed COVID-19, and infiltrates on chest imaging and/or oxygen saturation of ≤ 95% on room air were stratified by age group (< 65 years and ≥ 65 years), sex, and site and randomly assigned 1:1 within each stratum to receive either LY3127804 (20 mg/kg) or placebo on Day 1 and possibly on Day 15. The primary end point for this study was number of days in which a patient did not require a ventilator over the 28-day study period.
Results: Interim analysis assessed study futility after 95 randomized patients had 28-day data available and showed no benefit of LY3127804 in reducing the number of ventilator days over placebo. The study was subsequently terminated.
Conclusion: LY3127804 treatment did not decrease the need for ventilator usage in patients hospitalized with pneumonia and presumed or confirmed COVID-19.
Clinicaltrialsgov identifier: NCT04342897.
Keywords: Acute respiratory distress syndrome; Angiopoietin 2; COVID-19; SARS-CoV-2; pneumonia.
. 2022 Aug 10;16:11795484221119316.
doi: 10.1177/11795484221119316. eCollection 2022.
Efficacy and Safety of LY3127804, an Anti-Angiopoietin-2 Antibody, in a Randomized, Double-Blind, Placebo-Controlled Clinical Trial in Patients Hospitalized with Pneumonia and Presumed or Confirmed COVID-19
Rosie S Jones[SUP] 1 [/SUP], Patricia S Smith[SUP] 1 [/SUP], Paul H Berg[SUP] 1 [/SUP], Amparo de la Peña[SUP] 1 [/SUP], Paul P Cook[SUP] 2 [/SUP], Imad Shawa[SUP] 3 [/SUP], Kathleen M Kioussopoulos[SUP] 3 [/SUP], Yu Hu[SUP] 1 [/SUP], Robert J Schott[SUP] 1 [/SUP]
Affiliations
- PMID: 35991210
- PMCID: PMC9382233
- DOI: 10.1177/11795484221119316
Abstract
Background: Severe cases of coronavirus disease 2019 (COVID-19) are characterized by progressive respiratory failure and the development of acute respiratory distress syndrome (ARDS), with high mortality rates for patients requiring mechanical ventilation. Levels of the vascular growth factor Angiopoietin 2 (Ang2) in plasma have been strongly correlated with increased ARDS risk in patients with pneumonia or sepsis. The intent of this study was to determine whether LY3127804, an anti-Ang2 monoclonal antibody, could reduce the need for mechanical ventilation among patients admitted to the hospital with pneumonia and presumed or confirmed COVID-19.
Methods: Patients admitted to hospital with confirmed pneumonia, presumed or confirmed COVID-19, and infiltrates on chest imaging and/or oxygen saturation of ≤ 95% on room air were stratified by age group (< 65 years and ≥ 65 years), sex, and site and randomly assigned 1:1 within each stratum to receive either LY3127804 (20 mg/kg) or placebo on Day 1 and possibly on Day 15. The primary end point for this study was number of days in which a patient did not require a ventilator over the 28-day study period.
Results: Interim analysis assessed study futility after 95 randomized patients had 28-day data available and showed no benefit of LY3127804 in reducing the number of ventilator days over placebo. The study was subsequently terminated.
Conclusion: LY3127804 treatment did not decrease the need for ventilator usage in patients hospitalized with pneumonia and presumed or confirmed COVID-19.
Clinicaltrialsgov identifier: NCT04342897.
Keywords: Acute respiratory distress syndrome; Angiopoietin 2; COVID-19; SARS-CoV-2; pneumonia.