Anti-C5a antibody (vilobelimab) therapy for critically ill, invasively mechanically ventilated patients with COVID-19 (PANAMO): a multicentre, double-blind, randomised, placebo-controlled, phase 3 trial. Issue 12 (December 2022)

• Record Type: Journal Article
• Authors: Vlaar, Alexander P J; Witzenrath, Martin; van Paassen, Pieter; Heunks, Leo M A; Mourvillier, Bruno; de Bruin, Sanne; Lim, Endry H T; Brouwer, Matthijs C; Tuinman, Pieter R; Saraiva, José F K; Marx, Gernot; Lobo, Suzana M; Boldo, Rodrigo; Simon-Campos, Jesus A; Cornet, Alexander D; Grebenyuk, Anastasia; Engelbrecht, Johannes M; Mukansi, Murimisi; Jorens, Philippe G; Zerbib, Robert; Rückinger, Simon; Pilz, Korinna; Guo, Renfeng; van de Beek, Diederik; Riedemann, Niels C; Vlaar, Alexander P.J.; Witzenrath, Martin; van Paassen, Pieter; Heunks, Leo M.A.; Mourvillier, Bruno; de Bruin, Sanne; Lim, Endry H.T.; Brouwer, Matthijs C.; Tuinman, Pieter R.; Saraiva, José Francisco K.; Marx, Gernot; Lobo, Suzana; Boldo, Rodrigo; Simon-Campos, Jesus; Cornet, Alexander D.; Grebenyuk, Anastasia; Engelbrecht, Johannes; Mukansi, Murimisi; Jorens, Philippe G.; Zerbib, Robert; Rückinger, Simon; Pilz, Korinna; Guo, Renfeng; van de Beek, Diederik; Riedemann, Niels C.; Bulpa, Pierre; Taccone, Fabio S.; Hermans, Greet; Diltoer, Marc; Piagnerelli, Michael; De Neve, Nikolaas; Freire, Antonio T.; Pizzol, Felipe D.; Marinho, Anna Karolina; Sato, Victor H.; Arns da Cunha, Clovis; Neuville, Mathilde; Dellamonica, Jean; Annane, Djillali; Roquilly, Antoine; Diehl, Jean Luc; Schneider, Francis; Mira, Jean Paul; Lascarrou, Jean Baptiste; Desmedt, Luc; Dupuis, Claire; Schwebel, Carole; Thiéry, Guillaume; Gründling, Matthias; Berger, Marc; Welte, Tobias; Bauer, Michael; Jaschinski, Ulrich; Matschke, Klaus; Mercado-Longoria, Roberto; Gomez Quintana, Belinda; Zamudio-Lerma, Jorge Alberto; Moreno Hoyos Abril, Juan; Aleman Marquez, Angel; Pickkers, Peter; Otterspoor, Luuk; Hercilla Vásquez, Luis; Seas Ramos, Carlos Rafael; Peña Villalobos, Alejandro; Gianella Malca, Gonzalo; Chávez, Victoria; Filimonov, Victor; Kulabukhov, Vladimir; Acharya, Pinak; Timmermans, Sjoerd A.M.E.G.; Busch, Matthias H.; van Baarle, Floor L.F.; Koning, Rutger; ter Horst, Liora; Chekrouni, Nora; van Soest, Thijs M.; Slim, Marleen A.; van Vught, Lonneke A.; van Amstel, Rombout B.E.; Olie, Sabine E.; van Zeggeren, Ingeborg E.; van de Poll, Marcel C.G.; Thielert, Claus; Neukirchen, Dorothee;
• Is Part Of: Lancet. Volume 10:Issue 12(2022)
• Page Start: 1137
• Page End: 1146
• Publication Date: 2022-12
• Subjects: Respiratory organs -- Diseases -- Periodicals; 616.2005
• DOI: 10.1016/S2213-2600(22)00297-1
• Languages: English
• ISSNs: 2213-2600

Abstract

Summary: Background: Vilobelimab, an anti-C5a monoclonal antibody, was shown to be safe in a phase 2 trial of invasively mechanically ventilated patients with COVID-19. Here, we aimed to determine whether vilobelimab in addition to standard of care improves survival outcomes in this patient population. Methods: This randomised, double-blind, placebo-controlled, multicentre phase 3 trial was performed at 46 hospitals in the Netherlands, Germany, France, Belgium, Russia, Brazil, Peru, Mexico, and South Africa. Participants aged 18 years or older who were receiving invasive mechanical ventilation, but not more than 48 h after intubation at time of first infusion, had a PaO2 /FiO2 ratio of 60–200 mm Hg, and a confirmed SARS-CoV-2 infection with any variant in the past 14 days were eligible for this study. Eligible patients were randomly assigned (1:1) to receive standard of care and vilobelimab at a dose of 800 mg intravenously for a maximum of six doses (days 1, 2, 4, 8, 15, and 22) or standard of care and a matching placebo using permuted block randomisation. Treatment was not continued after hospital discharge. Participants, caregivers, and assessors were masked to group assignment. The primary outcome was defined as all-cause mortality at 28 days in the full analysis set (defined as all randomly assigned participants regardless of whether a patient started treatment, excluding patients randomly assigned in error) and measured using Kaplan-Meier analysis. Safety analyses included all patients who had received at least one infusion of either vilobelimab or placebo. This study is registered with ClinicalTrials.gov, NCT04333420 . Findings: From Oct 1, 2020, to Oct 4, 2021, we included 368 patients in the ITT analysis (full analysis set; 177 in the vilobelimab group and 191 in the placebo group). One patient in the vilobelimab group was excluded from the primary analysis due to random assignment in error without treatment. At least one dose of study treatment was given to 364 (99%) patients (safety analysis set). 54 patients (31%) of 177 in the vilobelimab group and 77 patients (40%) of 191 in the placebo group died in the first 28 days. The all-cause mortality rate at 28 days was 32% (95% CI 25–39) in the vilobelimab group and 42% (35–49) in the placebo group (hazard ratio 0·73, 95% CI 0·50–1·06; p=0·094). In the predefined analysis without site-stratification, vilobelimab significantly reduced all-cause mortality at 28 days (HR 0·67, 95% CI 0·48–0·96; p=0·027). The most common TEAEs were acute kidney injury (35 [20%] of 175 in the vilobelimab group vs 40 [21%] of 189 in the placebo), pneumonia (38 [22%] vs 26 [14%]), and septic shock (24 [14%] vs 31 [16%]). Serious treatment-emergent adverse events were reported in 103 (59%) of 175 patients in the vilobelimab group versus 120 (63%) of 189 in the placebo group. Interpretation: In addition to standard of care, vilobelimab improves survival of invasive mechanically ventilated patients with COVID-19 and leads to a significant decrease in mortality. Vilobelimab could be considered as an additional therapy for patients in this setting and further research is needed on the role of vilobelimab and C5a in other acute respiratory distress syndrome-causing viral infections. Funding: InflaRx and the German Federal Government.