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Written informed consent to participate in this study was provided by the participant\u2019s legal guardian\/next of kin. This project is conducted following the ICH Harmonized Tripartite Guidelines for Good Clinical Practice, with the current national regulations (Law 14\/2007 on Biomedical Research), and with the ethical principles established in the Declaration of Helsinki. The confidentiality of the data of the study participants will be guaranteed, ensuring compliance with Organic Law 3\/2018, of December 5, on the Protection of Personal Data and guarantee of digital rights.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethics approval and consent to participate"}},{"value":"Not Applicable.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Consent for publication"}},{"value":"Ana Isabel Dacosta Urbieta has participated in clinical trials for RSV vaccines and monoclonals with all honoraria paid to the institution. Irene Rivero Calle has received honoraria from GSK, Pfizer, Sanofi, and MSD for taking part in advisory boards and expert meetings and acting as a speaker in congresses outside the scope of the submitted work. IRC has also acted as sub-investigator in randomized controlled trials of Abbot, Astrazeneca, Enanta, Gilead, GlaxoSmithKline, Janssen, Medimmune, Merck, Moderna, MSD, Novavax, Pfizer, Reviral, Roche, Sanofi Pasteur, and Seqirus.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}}],"article-number":"25"}}