medRxiv preprint doi: https://doi.org/10.1101/2020.10.05.20206870; this version posted October 6, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-ND 4.0 International license . An open-label prospective observational study of antiandrogen and non-antiandrogen early pharmacological approaches in females with mild-to-moderate COVID-19. The Pre-AndroCoV Female Trial. Flavio A. Cadegiani1,2, Andy Goren3, Carlos G. Wambier4, John McCoy3 1 Adrenal and Hypertension Unit, Division of Endocrinology and Metabolism, Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo (EPM/UNIFESP), São Paulo, SP, Brazil 2Corpometria Institute, Brasília, DF, Brazil 3Applied Biology Inc., Irvine, CA, USA 4Brown University, RI, USA Address correspondence: Flavio A. Cadegiani, MD, MSc, PhD Division of Endocrinology and Metabolism, Department of Medicine, Escola Paulista de Medicina, Universidade Federal de São Paulo Rua Pedro de Toledo 781 – 13th floor, 04039-032 São Paulo, SP – Brazil Email:
[email protected] ;
[email protected] Telephone: +55 61 996506111, Fax: +55 61 33464733 Key-words: COVID-19, SARS-CoV-2, antiandrogen, dutasteride, spironolactone, Abstract Background: While COVID-19 remains largely unclear and mortality continues to raise, early effective approaches prior to complications lack, as well as researches for characterization and therapeutical potential options in actual early COVID-19. Although females seem to be less affected than females, hyperandrogenic (HA) phenotype, like polycystic ovary syndrome (PCOS), idiopathic hirsutism, congenital adrenal hyperplasia (CAH) female androgenetic alopecia (AGA), or idiopathic HA may be at higher risk due to its inherent enhanced androgenic activity.