Zubiaur, Pablo http://orcid.org/0000-0002-6150-4320
Kneller, Lisa A.
Ochoa, Dolores
Mejía, Gina http://orcid.org/0000-0002-8689-7941
Saiz-Rodríguez, Miriam http://orcid.org/0000-0002-1660-3135
Borobia, Alberto M. http://orcid.org/0000-0002-8584-3263
Koller, Dora http://orcid.org/0000-0002-0415-0466
García, Irene García
Navares-Gómez, Marcos http://orcid.org/0000-0003-2501-6845
Hempel, Georg http://orcid.org/0000-0002-5790-6423
Abad-Santos, Francisco http://orcid.org/0000-0002-6519-8885
Funding for this research was provided by:
H2020 Marie Skłodowska-Curie Actions (Innovative Training Network 721236)
Instituto de Salud Carlos III (Rio Hortega grant)
Consejería de Educación
Juventud y Deporte
Comunidad de Madrid
Article History
First Online: 17 September 2020
Declarations
:
: Dora Koller is financed by the H2020 Marie Skłodowska Curie Innovative Training Network 721236 grant. Irene García García is financed by Instituto de Salud Carlos III by the Rio Hortega grant. Marcos Navares-Gomez is co-financed by Consejería de Educación, Juventud y Deporte from Comunidad de Madrid and Fondo Social Europeo. No funds were received for the current research.
: Francisco Abad-Santos and Dolores Ochoa have been consultants or investigators in clinical trials sponsored by Abbott, Alter, Chemo, Cinfa, FAES, Farmalíder, Ferrer, GlaxoSmithKline, Galenicum, Gilead, Janssen-Cilag, Kern, Normon, Novartis, Servier, Silverpharma, Teva, and Zambon. Pablo Zubiaur, Lisa A. Kneller, Gina Mejía, Miriam Saiz-Rodríguez, Alberto M. Borobia, Dora Koller, Irene García García, Marcos Navares-Gómez, and Georg Hempel declare no conflicts of interest.
: Study protocols were approved by an independent Research Ethics Committee. In addition, the protocols were duly authorized by the Spanish Medicines Agency (AEMPS) and were carried out under the guidelines of Good Clinical Practices, complying with current Spanish legislation on clinical research in humans and with the Declaration of Helsinki. EUDRA-CT numbers: 2012–004029-26, 2014–001964-36, and 2014–005342-22.
: All subjects provided informed consent to participate in the present research.
: Data are available from the corresponding author upon reasonable request.