Acknowledgments
We acknowledge the study participants, their caregivers, and their medical providers. We also acknowledge the following for their contributions: Monika Deswal and Elnaz Eilkhani for regulatory support; the UCSF LIINC, RECOVER, and clinical trials teams especially Viva Tai, Khamal Anglin, Grace Anderson, Melissa Buitrago, Emily Conway, Avery Eun, and Megan Lew for participant referrals and coordination; the UCSF Investigational Drug Service, especially Scott Fields, for preparing and dispensing study product; the UCSF Parnassus Clinical Research Service (CRS), especially Josephine Liu, Ryan Gunay, Patricia Cannon, Beryl Abungan, and Allison Ingebretson for administering the study drug and monitoring participants; the UCSF Specimen Processing & Banking Subcore including Salman Mahboob and Billy Huang for overseeing biospecimen processing; the Henrich lab, especially Lilian Grimbert and Belen Altamirano Poblano for assistance with the tissue-based assays; Danny Li and Marty Levkova-Clark for assistance in performing the cardiopulmonary exercise tests; Safety Monitoring Committee members Vincent Marconi, Jason Goldman, and Rasika Karnik; Molly Beam for guidance on CNS-Vital Signs neurocognitive testing; the Mayo Foundation for Medical Education and Research for licensing the COMPASS-31 for use in the study; Lisa McCorkell and Hannah Davis from the Patient-Led Research Collaborative for advice in the design and implementation of the study; and Amy Proal for input on the manuscript.
Funding
The conduct of the clinical trial was financially supported by the Patient-Led Research Fund, a project of Patient-Led Research Collaborative funded by Balvi. The optional gut biopsy and imaging procedures were funded by the PolyBio Research Foundation. Additional biological measurements were supported by funding from the National Institute for Neurologic Disorders and Stroke (NINDS; R01NS136197) and the PolyBio Research Foundation. This project was supported by the National Center for Advancing Translational Sciences, National Institutes of Health, through UCSF-CTSI Grant Number UL1 TR001872. Sequencing was performed at the UCSF CAT, supported by UCSF PBBR, RRP IMIA, and NIH 1S10OD028511-01 grants. The contents of this manuscript are solely the responsibility of the authors and do not necessarily represent the official views of the NIH.
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Competing interests
M.J.P. has received consulting fees from Gilead Sciences, AstraZeneca, BioVie, Apellis Pharmaceuticals, BioNTech, and TechImmune, travel support from Invivyd, and research support from Shionogi, BioVie, and ImmunityBio, outside the submitted work. Y.F. reports a financial interest in Eugit Therapeutics, which is unrelated to the submitted work. M.S.D. has received consulting fees from Merck. D.G. has received consulting fees from Gilead, Merck, and Viiv. S.G.D. reports consulting for Enanta Pharmaceuticals and Pfizer. The remaining authors declare no competing interests.
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Peluso, M.J., Ryder, D., Dalhuisen, T. et al. SARS-CoV-2-specific monoclonal antibody AER002 in Long COVID: an exploratory randomized phase 2a mechanistic trial. Nat Commun (2026). https://doi.org/10.1038/s41467-026-77925-y
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DOI: https://doi.org/10.1038/s41467-026-77925-y