A structure-based mRNA vaccine for Nipah virus in healthy adults: a phase 1 trial

Nipah virus (NiV) is a highly pathogenic, zoonotic paramyxovirus with pandemic potential. No licensed vaccines or treatments are available. Therefore, we conducted a phase 1, first-in-human, open-label, dose-escalation trial of a lipid nanoparticle mRNA vaccine, mRNA-1215, encoding a chimeric pre-fusion F (Pre-F) protein linked to glycoprotein G of a NiV Malaysian strain. Forty healthy adults, who met eligibility criteria, were enrolled into the 10-, 25-, 50- or 100-μg dose groups with ten participants per group. Each participant received two doses of mRNA-1215, intramuscularly, at a 4-week interval except for one participant in the 10-μg dose group who received only the first dose. All participants remained in the study until their final study visit. The primary outcome of vaccine safety and tolerability was determined by prespecified end points: the frequency and severity of solicited local and systemic adverse events (AEs), unsolicited AEs, safety laboratory measures, medically attended AEs, AEs of special interest, new chronic medical conditions and serious AEs. The most frequently reported local and systemic AEs were mild pain and tenderness at the injection site (n = 33; 82%) and mild malaise (n = 16; 40%), respectively. Overall, the vaccine was well tolerated. No serious AEs occurred during the study. mRNA-1215 elicited robust Pre-F and G binding antibody titers, the prespecified secondary end points. An exploratory analysis found that mRNA-1215 elicited neutralizing titers by 2 weeks after the prime in all dose groups. Responses increased after the boost and remained elevated for at least 1 year after vaccination. These findings demonstrate an initial overall favorable safety profile and immunogenicity results for a first-in-human, structure-based, chimeric mRNA Nipah virus vaccine. mRNA-1215 is a promising vaccine candidate for continued clinical development for populations at risk for regional and potentially larger outbreaks caused by Nipah virus. ClinicalTrials.gov identifier: NCT05398796 .

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Journal
Nature Medicine
Published
2026-03-12
DOI
https://doi.org/10.1038/s41591-026-04265-1
Primary Topic
Virology and Viral Diseases
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article
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0.00

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article

A structure-based mRNA vaccine for Nipah virus in healthy adults: a phase 1 trial

Tongqing Zhou, LaShawn Requilman, Joanna Utoh, Abidemi Ola et al.
Nature Medicine
Virology and Viral Diseases
article

A structure-based mRNA vaccine for Nipah virus in healthy adults: a phase 1 trial

Tongqing Zhou, LaShawn Requilman, Joanna Utoh, Abidemi Ola, Pamela Costner, Rosemarie D. Mason, Rebecca J. Loomis, Jennifer Cunningham, Alicia T. Widge, Alan Heimann, Lesia Dropulic, Preeti Apte, Sunny Himansu, Emily E. Coates, Kathryn E. Foulds, Jessica Bahorich, Galina V. Yamshchikov, Aurélie Ploquin, Caitlyn N M Dulan, Walla Dempsey, Karin Bok, Ingelise J. Gordon, Tatiana Beresnev, Brett Leav, Shayne F. Andrew, X.L. Wang, Ana M. Ortega-Villa, Evan R. Lamb, Larisa Strom, Renunda Dyer, Floreliz Mendoza, Mary Kay McDonald, Katia G. Korzeniwsky, I-Ting Teng, LaSonji A. Holman, Lorin N. Loftus, Maryam Keshtkar-Jahromi, Justine Jones, Laura Novik, Barney S. Graham, Amelia Thompson, Anita Arthur, Myra Happe, Shruthi Shyam Sunder, John H. Beigel, Jamie Saunders, Li Ou, Maxwell Norris, William R. Whalen, Nancy J. Sullivan, Mario Roederer, The VRC 322 study team
article en

Abstract

Nipah virus (NiV) is a highly pathogenic, zoonotic paramyxovirus with pandemic potential. No licensed vaccines or treatments are available. Therefore, we conducted a phase 1, first-in-human, open-label, dose-escalation trial of a lipid nanoparticle mRNA vaccine, mRNA-1215, encoding a chimeric pre-fusion F (Pre-F) protein linked to glycoprotein G of a NiV Malaysian strain. Forty healthy adults, who met eligibility criteria, were enrolled into the 10-, 25-, 50- or 100-μg dose groups with ten participants per group. Each participant received two doses of mRNA-1215, intramuscularly, at a 4-week interval except for one participant in the 10-μg dose group who received only the first dose. All participants remained in the study until their final study visit. The primary outcome of vaccine safety and tolerability was determined by prespecified end points: the frequency and severity of solicited local and systemic adverse events (AEs), unsolicited AEs, safety laboratory measures, medically attended AEs, AEs of special interest, new chronic medical conditions and serious AEs. The most frequently reported local and systemic AEs were mild pain and tenderness at the injection site (n = 33; 82%) and mild malaise (n = 16; 40%), respectively. Overall, the vaccine was well tolerated. No serious AEs occurred during the study. mRNA-1215 elicited robust Pre-F and G binding antibody titers, the prespecified secondary end points. An exploratory analysis found that mRNA-1215 elicited neutralizing titers by 2 weeks after the prime in all dose groups. Responses increased after the boost and remained elevated for at least 1 year after vaccination. These findings demonstrate an initial overall favorable safety profile and immunogenicity results for a first-in-human, structure-based, chimeric mRNA Nipah virus vaccine. mRNA-1215 is a promising vaccine candidate for continued clinical development for populations at risk for regional and potentially larger outbreaks caused by Nipah virus. ClinicalTrials.gov identifier: NCT05398796 .

Nature Medicine
Moderna Therapeutics (United States) (US), National Institute of Allergy and Infectious Diseases (US)
U.S. Department of Health and Human Services, Coalition for Epidemic Preparedness Innovations, Moderna, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases
Good health and well-being
Openalex Percentile: Top 26%
Virology and Viral Diseases
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