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166. A Phase 2b/3 Study to Evaluate the Efficacy and Safety of an Investigational Respiratory Syncytial Virus (RSV) Antibody, Clesrovimab, in Healthy Preterm and Full-Term Infants

Heather J. Zar, Eric A. F. Simões, Sabhir Madhi, Octavio Ramilo, Shelly Senders, Julie S. Shepard, Kamolwish Laoprasopwattana, Jorge A. Piedrahita, Jose M Novoa Pizarro, Sergio L. Vargas, Marc Dionne, Teresa Jackowska, Enmei Liu, Yasunori Ishihara, Kazushige Ikeda, Ying Zhang, Radha Railkar, Jeannine Lutkiewicz, Andrew W. Lee, Andrea Guerra, Anushua Sinha

2025Open Forum Infectious Diseases18 citationsDOIOpen Access PDF

Abstract

Abstract Background Clesrovimab is an investigational, long-acting monoclonal antibody (mAb) targeting site IV of the fusion protein for the prevention of RSV lower respiratory tract infection in infants. Methods This phase 2b/3 double-blind, randomized, placebo-controlled pivotal study enrolled healthy preterm and full-term infants birth to 1 year of age entering their first RSV season. Participants (pts) were randomized 2:1 to receive clesrovimab (105 mg IM) or placebo on day 1. Safety and tolerability were a primary endpoint. There were two hypothesis-tested endpoints: the efficacy of clesrovimab against RSV-associated medically attended lower respiratory tract infection (MALRI) through day 150 (primary) and against RSV-associated hospitalization through day 150 (secondary). The MALRI definition required ≥1 indicators of lower respiratory tract infection (LRI) or severity. To facilitate comparison across RSV mAb trials, a definition of RSV-associated MALRI that required ≥2 indicators of LRI/severity (≥1 indicator of LRI and ≥1 indicator of severity) was assessed post hoc. Results There were 3,632 pts randomized across 22 countries; >99% received study intervention. RSV-associated efficacy endpoints through day 150 and day 180 are shown in Table 1. Clesrovimab reduced the incidence of RSV-associated MALRI requiring ≥1 indicator of LRI/severity (60.4% [95% CI: 44.1, 71.9], p< 0.001) and ≥2 indicators of LRI/severity (88.0% [95% CI:76.1, 94.0]), RSV hospitalization (84.2% [95% CI: 66.6, 92.6], p< 0.001), and severe MALRI (91.7% [95% CI:62.9, 98.1]) through day 150 postdose compared to placebo. Efficacy increased with increasing RSV-associated disease severity and was similar from days 1-180 compared to days 1-150 across endpoints. The proportions of pts with adverse events (AEs), including injection-site and systemic AEs, drug-related AEs, and serious AEs were comparable between the clesrovimab and placebo groups (Table 2). There were no treatment-related deaths or deaths attributed to RSV disease. Conclusion A single dose of clesrovimab given before or during the first RSV season was efficacious in reducing RSV-associated MALRI and RSV-associated hospitalization in healthy preterm and full-term infants and was generally well tolerated with a safety profile comparable to placebo. Disclosures Heather J. Zar, PhD, MSD, Pfizer, AstraZeneca, Moderna (DSMB): Advisor/Consultant|MSD, Pfizer, AstraZeneca, Moderna (DSMB): Grant/Research Support|MSD, Pfizer, AstraZeneca, Moderna (DSMB): Honoraria|MSD, Pfizer, AstraZeneca, Moderna (DSMB): MSD Principal Investigator for the study and on MSD Advisory Board Eric Simoes, MD DCH, Pfizer, Sanofi, Merck, Icosavax, Enanta Cidara, Adiagio, Nuance, Shionogi, GIlead,: Advisor/Consultant|Pfizer, Sanofi, Merck, Icosavax, Enanta Cidara, Adiagio, Nuance, Shionogi, GIlead,: Grant/Research Support|Pfizer, Sanofi, Merck, Icosavax, Enanta Cidara, Adiagio, Nuance, Shionogi, GIlead,: Honoraria|Pfizer, Sanofi, Merck, Icosavax, Enanta Cidara, Adiagio, Nuance, Shionogi, GIlead,: MSD - PI for this study; DSMB Abbvie, Moderna, GSK Sabhir Madhi, MD, Pfizer, GSK, Medimmune, Merck & Co., Inc., Rahway, NJ, USA: Grant/Research Support|Pfizer, GSK, Medimmune, Merck & Co., Inc., Rahway, NJ, USA: Honoraria Octavio Ramilo, MD, Pfizer, Sanofi, Gates Foundation, NIH, and Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA (MSD): Advisor/Consultant|Pfizer, Sanofi, Gates Foundation, NIH, and Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA (MSD): Grant/Research Support|Pfizer, Sanofi, Gates Foundation, NIH, and Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA (MSD): Honoraria|Pfizer, Sanofi, Gates Foundation, NIH, and Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA (MSD): SAC member for MSD Shelly Senders, MD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Principal Investigator Julie S. Shepard, MD, MPH, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Principal Investigator Kamolwish Laoprasopwattana, MD, Merck & Co., Inc., Rahway, NJ, USA: Grant/Research Support|Merck & Co., Inc., Rahway, NJ, USA: MSD - PI for this study Jorge Piedrahita, MD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Principal Investigator Jose M. Novoa Pizarro, MD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA (MSD): Principal Investigator for the study for MSD Sergio L. Vargas, MD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Principal Investigator Marc Dionne, MD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Principal Investigator Teresa Jackowska, MD, MSD Poland, Merck & Co., Inc, Rahway, NJ, USA: Advisor/Consultant|MSD Poland, Merck & Co., Inc, Rahway, NJ, USA: Grant/Research Support|MSD Poland, Merck & Co., Inc, Rahway, NJ, USA: Honoraria|MSD Poland, Merck & Co., Inc, Rahway, NJ, USA: MSD - PI for this study Enmei Liu, MD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Principal Investigator Yasunori Ishihara, MD, PhD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Principal Investigator Kazushige Ikeda, MD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Principal Investigator Ying Zhang, PhD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Employee|Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Stocks/Bonds (Public Company) Radha A. Railkar, PhD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, US (MSD): Employee|Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, US (MSD): Stocks/Bonds (Public Company) Jeannine Lutkiewicz, BS, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Employee|Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Stocks/Bonds (Public Company) Andrew W. Lee, MD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA (MSD): Employee at the time of study|Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA (MSD): Stocks/Bonds (Public Company) Andrea Guerra, MD, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Employee|Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA: Stocks/Bonds (Public Company) Anushua Sinha, MD, MPH, Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA (MSD): Employee|Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA (MSD): Stocks/Bonds (Public Company)

Topics & Concepts

MedicineRespiratory systemVirologyAntibodyFull TermPediatricsImmunologyInternal medicinePregnancyBiologyGeneticsRespiratory viral infections researchImmunodeficiency and Autoimmune DisordersNeonatal Respiratory Health Research