Efficacy and safety of CD24Fc in hospitalised patients with COVID-19: a randomised, double-blind, placebo-controlled, phase 3 study. Issue 5 (May 2022)

• Record Type: Journal Article
• Authors: Welker, James; Pulido, Juan D; Catanzaro, Andrew T; Malvestutto, Carlos D; Li, Zihai; Cohen, Jonathan B; Whitman, Eric D; Byrne, Dana; Giddings, Olivia K; Lake, Jordan E; Chua, Joel V; Li, Ella; Chen, Jian; Zhou, Xiang; He, Kun; Gates, Davis; Kaur, Amarjot; Chen, Jamie; Chou, Hung-Yen; Devenport, Martin; Touomou, Raymond; Kottilil, Shyamasundaran; Liu, Yang; Zheng, Pan; Zheng, Pan; Liu, Yang; Devenport, Martin; Touomou, Raymond; Chou, Hung-Yen; Thakor, Jai; Khan, Imaan; Do, Nicole; Faragalla, Josephine; Hook, Andrea; Kern, Sarah; Ramos, Janira V.; Ward, Jason; Chen, Jamie; Higson, John; Dam, Meena; Serkin, Dawn; Karloopia, Pooja; Moore, Wendy; Scofield, Mark; Childers, David Jeffery; Cantrell, Jeffrey S.; Corgan, Millie; Li, Ella; Chen, Jian; Zhou, Xiang; Liu, Jing; Redvers-Higgins, Denise; Han, Hua; Hou, Jiyun; Pan, Yudi; Tucker, Karyn; Zhang, Xiaoyan; Kottilil, Shyamasundaran; Chua, Joel V.; Husson, Jennifer; Narayanan, Shivakumar; Bran, Jaqueline; Lam, Ka Wing Joyce; Jeffrey, Alicia; Giddings, Olivia K.; Pexa, Jennie; Becerra, Mario; Welker, James; Gray, Kathleen W.; Richmond, Nicole; Nzelibe, Chukwuemeka; Malvestutto, Carlos D.; Koletar, Susan; Sobhanie, Mahdee; Clark, Jan; Li, Zihai; Reynolds, Kelsi; Chakravarthy, Karthik; Weller, Kevin; Yusuf, Mohamed; Severing, Jennifer; Barley, Kelley; Pulido, Juan D.; Fulton, Jennifer C.; Gil, William; Jeanine, M.D.; R.N., Richmond; Jones, Sandy; Clemmer, Kristina; Byrne, Dana; Pedroza, Lisa; Davidson, Emily Nicole; Logan, Amanda; Grant, Katie; Whitman, Eric D.; Kessler, Jason; Roland, Robert; Stefiniw, Rosemary; Maurer, Molly; Geene, Salome; Buck, Christopher F.; Connolly, Debra; Light, Patrice; Baviskar, Sunanda; Low, Yee Won; Michalski, Kyra; Giordano, Pamela; Chao, Jennifer; Williams, Michelle; Makkapati, Amulya; Catanzaro, Andrew T.; Cohen, Jonathan B.; Musbah, Mehad; Jaladanki, Pramila; Yuan, Ying; Rele, Shilpa; Stewart, Desirae; Lewis, Starlet; Sankar, Ian; Kasumba, Nabulungi; Biney, Kaylia; Hekmat, Elham; Lake, Jordan E.; Akkanti, Bindu; Reimer-McAtee, Melissa J.; Negret Hernandez, Marisel;
• Is Part Of: Lancet infectious diseases. Volume 22:Issue 5(2022)
• Page Start: 611
• Page End: 621
• Publication Date: 2022-05
• Subjects: Communicable diseases -- Periodicals; Infection -- Periodicals; Communicable Diseases -- Periodicals; Infection -- Periodicals; Maladies infectieuses -- Périodiques; Infection -- Périodiques; Communicable diseases; Infection; Periodicals; 616.905
• DOI: 10.1016/S1473-3099(22)00058-5
• Languages: English
• ISSNs: 1473-3099

Abstract

Summary: Background: Non-antiviral therapeutic options are required for the treatment of hospitalised patients with COVID-19. CD24Fc is an immunomodulator with potential to reduce the exaggerated inflammatory response to tissue injuries. We aimed to evaluate the safety and efficacy of CD24Fc in hospitalised adults with COVID-19 receiving oxygen support. Methods: We conducted a randomised, double-blind, placebo-controlled, phase 3 study at nine medical centres in the USA. Hospitalised patients (age ≥18 years) with confirmed SARS-CoV-2 infection who were receiving oxygen support and standard of care were randomly assigned (1:1) by site-stratified block randomisation to receive a single intravenous infusion of CD24Fc 480 mg or placebo. The study funder, investigators, and patients were masked to treatment group assignment. The primary endpoint was time to clinical improvement over 28 days, defined as time that elapsed between a baseline National Institute of Allergy and Infectious Diseases ordinal scale score of 2–4 and reaching a score of 5 or higher or hospital discharge. The prespecified primary interim analysis was done when 146 participants reached the time to clinical improvement endpoint. Efficacy was assessed in the intention-to-treat population. Safety was assessed in the as-treated population. This study is registered with ClinicalTrials.gov, NCT04317040 . Findings: Between April 24 and Sept 22, 2020, 243 hospitalised patients were assessed for eligibility and 234 were enrolled and randomly assigned to receive CD24Fc (n=116) or placebo (n=118). The prespecified interim analysis was done when 146 participants reached the time to clinical improvement endpoint among 197 randomised participants. In the interim analysis, the 28-day clinical improvement rate was 82% (81 of 99) for CD24Fc versus 66% (65 of 98) for placebo; median time to clinical improvement was 6·0 days (95% CI 5·0–8·0) in the CD24Fc group versus 10·0 days (7·0–15·0) in the placebo group (hazard ratio [HR] 1·61, 95% CI 1·16–2·23; log-rank p=0·0028, which crossed the prespecified efficacy boundary [α=0·0147]). 37 participants were randomly assigned after the interim analysis data cutoff date; among the 234 randomised participants, median time to clinical improvement was 6·0 days (95% CI 5·0–9·0) in the CD24Fc group versus 10·5 days (7·0–15·0) in the placebo group (HR 1·40, 95% CI 1·02–1·92; log-rank p=0·037). The proportion of participants with disease progression within 28 days was 19% (22 of 116) in the CD24Fc group versus 31% (36 of 118) in the placebo group (HR 0·56, 95% CI 0·33–0·95; unadjusted p=0·031). The incidences of adverse events and serious adverse events were similar in both groups. No treatment-related adverse events were observed. Interpretation: CD24Fc is generally well tolerated and accelerates clinical improvement of hospitalised patients with COVID-19 who are receiving oxygen support. These data suggest that targeting inflammation in response to tissue injuries might provide a therapeutic option for patients hospitalised with COVID-19. Funding: Merck & Co, National Cancer Institute, OncoImmune.