Pre-exposure prophylaxis with hydroxychloroquine for COVID-19: a double-blind, placebo-controlled randomized clinical trial

被引:11
|
作者
Grau-Pujol, Berta [1 ,2 ,3 ]
Camprubi-Ferrer, Daniel [1 ]
Marti-Soler, Helena [1 ]
Fernandez-Pardos, Marc [1 ]
Carreras-Abad, Clara [1 ]
Velasco-de Andres, Maria [1 ]
Ferrer, Elisabet [1 ]
Muelas-Fernandez, Magdalena [1 ]
Jullien, Sophie [1 ]
Barilaro, Giuseppe [1 ]
Ajanovic, Sara [1 ]
Vera, Isabel [1 ]
Moreno, Laura [4 ]
Gonzalez-Redondo, Eva [4 ]
Cortes-Serra, Nuria [1 ]
Roldan, Montserrat [1 ]
Artes-de Arcos, Ana [1 ]
Mur, Isabel [5 ]
Domingo, Pere [5 ]
Garcia, Felipe [4 ,6 ]
Guinovart, Caterina [1 ]
Munoz, Jose [1 ]
机构
[1] Univ Barcelona, Barcelona Inst Global Hlth ISGlobal, Hosp Clin, Rossello 132 4rt 1a, Barcelona 08036, Spain
[2] Ctr Invest Saude Manhica CISM, Maputo, Mozambique
[3] Mundo Sano Fdn, Buenos Aires, DF, Argentina
[4] Univ Barcelona, Hosp Clin, Infect Dis Dept, IDIBAPS, Barcelona, Spain
[5] Hosp Santa Creu & Sant Pau, Infect Dis Unit, Inst Invest Biomed St Pau, Barcelona 08025, Spain
[6] Univ Barcelona, Hosp Clin, IDIBAPS, Aids Res Grp,Retrovirol & Viral Immunopathol, Barcelona, Spain
关键词
Hydroxychloroquine; COVID-19; Pre-exposure prophylaxis; Prevention; Health-care workers; Control; SARS-CoV-2; SYSTEMIC-LUPUS-ERYTHEMATOSUS; RHEUMATOID-ARTHRITIS;
D O I
10.1186/s13063-021-05758-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Pre-exposure prophylaxis (PrEP) is a promising strategy to break COVID-19 transmission. Although hydroxychloroquine was evaluated for treatment and post-exposure prophylaxis, it is not evaluated for COVID-19 PrEP yet. The aim of this study was to evaluate the efficacy and safety of PrEP with hydroxychloroquine against placebo in healthcare workers at high risk of SARS-CoV-2 infection during an epidemic period. Methods: We conducted a double-blind placebo-controlled randomized clinical trial in three hospitals in Barcelona, Spain. From 350 adult healthcare workers screened, we included 269 participants with no active or past SARS-CoV-2 infection (determined by a negative nasopharyngeal SARS-CoV-2 PCR and a negative serology against SARS-CoV-2). Participants allocated in the intervention arm (PrEP) received 400 mg of hydroxychloroquine daily for the first four consecutive days and subsequently, 400 mg weekly during the study period. Participants in the control group followed the same treatment schedule with placebo tablets. Results: 52.8% (142/269) of participants were in the hydroxychloroquine arm and 47.2% (127/269) in the placebo arm. Given the national epidemic incidence decay, only one participant in each group was diagnosed with COVID-19. The trial was stopped due to futility and our study design was deemed underpowered to evaluate any benefit regarding PrEP efficacy. Both groups showed a similar proportion of participants experiencing at least one adverse event (AE) (p=0.548). No serious AEs were reported. Almost all AEs (96.4%, 106/110) were mild. Only mild gastrointestinal symptoms were significantly higher in the hydroxychloroquine arm compared to the placebo arm (27.4% (39/142) vs 15.7% (20/127), p=0.041). Conclusions: Although the efficacy of PrEP with hydroxychloroquine for preventing COVID-19 could not be evaluated, our study showed that PrEP with hydroxychloroquine at low doses is safe.
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页数:10
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