Serum Virus-Neutralizing Antibody Titers in Clinical Trial Participants With and Without Immunocompromise Receiving Pemivibart, a Long-Acting Monoclonal Antibody for COVID-19

Narayan et al., The Journal of Infectious Diseases, doi:10.1093/infdis/jiag269, CANOPY, NCT06039449, May 2026
Analysis of 786 participants from the phase 3 CANOPY trial showing that pemivibart increased serum virus-neutralizing antibody titers against dominant circulating SARS-CoV-2 variants in both immunocompromised and non-immunocompromised patients.
Efficacy is variant dependent. In Vitro research shows reduced efficacy against KP.3.1.1, KP.1.1, LB.1, KP.3.3, and XEC variants1-4.
Narayan et al., 21 May 2026, Randomized Controlled Trial, USA, peer-reviewed, 7 authors, study period September 2023 - November 2024, trial NCT06039449 (history) (CANOPY). Contact: knarayan@invivyd.com.
Abstract: MAJOR ARTICLE Serum Virus-Neutralizing Antibody Titers in Clinical Trial Participants With and Without Immunocompromise Receiving Pemivibart, a Long-Acting Monoclonal Antibody for COVID-19 Kristin Narayan, 1, Kazima Tosh, 1 Anna Holmes, 1 Leijun Hu, 2 Sandeep Reddy Dkottam, 1 Ilker Yalcin, 1 and Mark Wingertzahn 1 1 Invivyd, Inc., New Haven, Connecticut, USA; and 2 LH Pharmaceutical Consulting, LLC, Carmel, Indiana, USA Background. Pemivibart received emergency use authorization for COVID-19 prevention in certain individuals with immunocompromise based on immunobridging calculated serum virus-neutralizing antibody (csVNA) titers. We report an analysis of measured (msVNA) titers against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants before and after receipt of pemivibart in a SARS-CoV-2 immune-experienced population (CANOPY) and compare the relationship between csVNA and msVNA titers in 2 clinical trials. Methods. The trials were conducted during 2023 -2024. In the phase 3 CANOPY trial, participants with (cohort A) or without (cohort B) significant immunocompromise received 2 intravenous 4500-mg pemivibart or placebo infusions 90 days apart. In the phase 1 trial, healthy adults received a single intravenous dose of pemivibart (1500, 2500, or 4500 mg). msVNA titers were determined using a SARS-CoV-2 spike pseudotyped assay; csVNA titers were calculated as serum pemivibart concentrations divided by variant-specific IC50 values from in vitro neutralization assays. Results. In CANOPY, predose msVNA geometric mean titers (GMTs) to the dominant circulating XBB.1.5 lineage were low across cohorts (range, 78.6 -119.8), suggesting inadequate protection. msVNA titers were substantially higher against earlier Delta (B.1.617.2) and BA.4/5 variants. Pemivibart increased the day-28 msVNA GMT > 55-fold against XBB.1.5, with similar levels in both cohorts. Across trials, csVNA titers were significantly correlated with msVNA titers (all Spearman correlation coefficients ≥ 0.73, P < .0001). Conclusions. These data show that previous immune experience to earlier pandemic variants provided limited cross-protection and demonstrate that pemivibart increased protective titers against newly circulating SARS-CoV-2 in individuals with and without immunocompromise. Notably, csVNA titers effectively predicted pemivibart ' s neutralization potential. Clinical Trials Registration. NCT06039449 and NCT05791318. Keywords. COVID-19; SARS-CoV-2; monoclonal antibody; pemivibart; serum virus-neutralizing titers. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) continues to cause significant illness and mortality from COVID-19 [1 -4]. Individuals with immunocompromise and adults aged ≥ 65 years remain at high risk for severe disease [5 -7] and hospitalization [8], highlighting an ongoing need for effective COVID-19 prevention. Serum virus-neutralizing antibody (sVNA) titers are a welldocumented correlate of protection against symptomatic Received 13 February 2026; accepted 14 May 2026; published online 21 May 2026 Correspondence: Kristin Narayan, PhD, Invivyd, Inc., 209 Church Street, New Haven, CT 06510 (knarayan@invivyd.com). The Journal of Infectious Diseases ® © The Author(s) 2026. Published by Oxford University Press on behalf of Infectious Diseases Society of America. This is an Open Access article..
DOI record: { "DOI": "10.1093/infdis/jiag269", "ISSN": [ "0022-1899", "1537-6613" ], "URL": "http://dx.doi.org/10.1093/infdis/jiag269", "abstract": "<jats:title>Abstract</jats:title>\n <jats:sec>\n <jats:title>Background</jats:title>\n <jats:p>Pemivibart received emergency use authorization for COVID-19 prevention in certain individuals with immunocompromise based on immunobridging calculated serum virus-neutralizing antibody (csVNA) titers. We report an analysis of measured (msVNA) titers against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants before and after receipt of pemivibart in a SARS-CoV-2 immune-experienced population (CANOPY) and compare the relationship between csVNA and msVNA titers in 2 clinical trials.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Methods</jats:title>\n <jats:p>The trials were conducted during 2023–2024. In the phase 3 CANOPY trial, participants with (cohort A) or without (cohort B) significant immunocompromise received 2 intravenous 4500-mg pemivibart or placebo infusions 90 days apart. In the phase 1 trial, healthy adults received a single intravenous dose of pemivibart (1500, 2500, or 4500 mg). msVNA titers were determined using a SARS-CoV-2 spike pseudotyped assay; csVNA titers were calculated as serum pemivibart concentrations divided by variant-specific IC50 values from in vitro neutralization assays.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Results</jats:title>\n <jats:p>In CANOPY, predose msVNA geometric mean titers (GMTs) to the dominant circulating XBB.1.5 lineage were low across cohorts (range, 78.6–119.8), suggesting inadequate protection. msVNA titers were substantially higher against earlier Delta (B.1.617.2) and BA.4/5 variants. Pemivibart increased the day-28 msVNA GMT &amp;gt;55-fold against XBB.1.5, with similar levels in both cohorts. Across trials, csVNA titers were significantly correlated with msVNA titers (all Spearman correlation coefficients ≥0.73, P &amp;lt; .0001).</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>Conclusions</jats:title>\n <jats:p>These data show that previous immune experience to earlier pandemic variants provided limited cross-protection and demonstrate that pemivibart increased protective titers against newly circulating SARS-CoV-2 in individuals with and without immunocompromise. Notably, csVNA titers effectively predicted pemivibart's neutralization potential.</jats:p>\n <jats:p>Clinical Trials Registration. NCT06039449 and NCT05791318.</jats:p>\n </jats:sec>", "article-number": "jiag269", "author": [ { "ORCID": "https://orcid.org/0000-0002-7977-4783", "affiliation": [ { "name": "Invivyd, Inc. , New Haven, Connecticut ,", "place": [ "USA" ] } ], "authenticated-orcid": false, "family": "Narayan", "given": "Kristin", "role": [ { "role": "author", "vocabulary": "crossref" } ], "sequence": "first" }, { "affiliation": [ { "name": "Invivyd, Inc. , New Haven, Connecticut ,", "place": [ "USA" ] } ], "family": "Tosh", "given": "Kazima", "role": [ { "role": "author", "vocabulary": "crossref" } ], "sequence": "additional" }, { "affiliation": [ { "name": "Invivyd, Inc. , New Haven, Connecticut ,", "place": [ "USA" ] } ], "family": "Holmes", "given": "Anna", "role": [ { "role": "author", "vocabulary": "crossref" } ], "sequence": "additional" }, { "affiliation": [ { "name": "LH Pharmaceutical Consulting, LLC , Carmel, Indiana ,", "place": [ "USA" ] } ], "family": "Hu", "given": "Leijun", "role": [ { 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