Experimental Treatment with Favipiravir for Ebola Virus Disease (the JIKI Trial): A Historically Controlled, Single-Arm Proof-of-Concept Trial in Guinea

被引:382
作者
Sissoko, Daouda [1 ,2 ]
Laouenan, Cedric [3 ,4 ]
Folkesson, Elin [5 ]
M'Lebing, Abdoul-Bing [6 ]
Beavogui, Abdoul-Habib [7 ]
Baize, Sylvain [8 ,9 ]
Camara, Alseny-Modet [5 ]
Maes, Piet [10 ,11 ]
Shepherd, Susan [6 ]
Danel, Christine [1 ,6 ,12 ]
Carazo, Sara [5 ]
Conde, Mamoudou N. [6 ]
Gala, Jean-Luc [13 ,14 ,15 ,16 ]
Colin, Geraldine [1 ,12 ,17 ]
Savini, Helene [18 ]
Bore, Joseph Akoi [10 ,19 ,20 ]
Le Marcis, Frederic [21 ]
Koundouno, Fara Raymond [10 ,19 ,20 ]
Petitjean, Frederic [6 ]
Lamah, Marie-Claire [5 ]
Diederich, Sandra [10 ,22 ]
Tounkara, Alexis [5 ]
Poelart, Geertrui [5 ]
Berbain, Emmanuel [5 ]
Dindart, Jean-Michel [6 ]
Duraffour, Sophie [10 ,11 ]
Lefevre, Annabelle [5 ]
Leno, Tamba [5 ]
Peyrouset, Olivier [6 ]
Irenge, Leonid [13 ,16 ]
Bangoura, N'Famara [5 ]
Palich, Romain [6 ]
Hinzmann, Julia [10 ,23 ]
Kraus, Annette [10 ,24 ]
Barry, Thierno Sadou [6 ]
Berette, Sakoba [6 ]
Bongono, Andre [6 ]
Camara, Mohamed Seto [6 ]
Munoz, Valerie Chanfreau [6 ]
Doumbouya, Lancine [6 ]
Harouna, Souley [6 ]
Kighoma, Patient Mumbere [6 ]
Koundouno, Fara Roger [6 ]
Lolamou, Rene [6 ]
Loua, Cece Moriba [6 ]
Massala, Vincent [6 ]
Moumouni, Kinda [6 ]
Provost, Celia [6 ]
Samake, Nenefing [6 ]
Sekou, Conde [6 ]
机构
[1] Univ Bordeaux, INSERM, UMR 1219, Bordeaux, France
[2] Ctr Hosp Univ Bordeaux, Bordeaux, France
[3] Univ Paris Diderot, INSERM, IAME, UMR 1137, Paris, France
[4] Hop Bichat Claude Bernard, AP HP, F-75877 Paris 18, France
[5] Med Sans Frontieres Belgique, Brussels, Belgium
[6] ALIMA, Dakar, Senegal
[7] Ctr Rech Sante Rurale, Maferinya, Guinea
[8] Ctr Int Rech Infectiol, Inst Pasteur, Lyon, France
[9] INSERM, Lab Jean Merieux P4, F-69008 Lyon, France
[10] European Mobile Lab Project, Hamburg, Germany
[11] Rega Inst Med Res, Leuven, Belgium
[12] Programme PACCI, Abidjan, Cote Ivoire
[13] Belgian First Aid & Support B FAST, Biol Light Fieldable Lab Emergencies B LiFE Belgi, Brussels, Belgium
[14] Clin Univ St Luc, B-1200 Brussels, Belgium
[15] Catholic Univ Louvain, Louvain La Neuve, Belgium
[16] Belgian Minist Def, Brussels, Belgium
[17] Croix Rouge Francaise, Paris, France
[18] Serv Sante Armees, Paris, France
[19] Inst Natl Sante Publ, Conakry, Guinea
[20] Univ Gamal Abdel Nasser Conakry, Lab Fievres Hemorrag Guinee, Conakry, Guinea
[21] Ecole Normale Super Lyon, F-69364 Lyon, France
[22] Fed Res Inst Anim Hlth, Friedrich Loeffler Inst, Greifswald, Germany
[23] Robert Koch Inst, Berlin, Germany
[24] Publ Hlth Agcy Sweden, Solna, Sweden
[25] Hop Necker Enfants Malad, AP HP, Paris, France
[26] Univ Montreal, Montreal, PQ, Canada
[27] Hop Bicetre, AP HP, Paris, France
[28] Publ Hlth England, Porton Down, Wilts, England
[29] Bernhard Nocht Inst Trop Med, Bernhard Nocht Str 74, D-20359 Hamburg, Germany
[30] Natl Inst Infect Dis L Spallanzani, Rome, Italy
[31] Bundeswehr Inst Microbiol, Munich, Germany
[32] Solidarite Therapeut & Initiat Sante Solthis, Paris, France
[33] INSERM, Paris, France
[34] Univ Southampton, Southampton Gen Hosp, Southampton, Hants, England
[35] Ctr Hosp Univ Treichville, Abidjan, Cote Ivoire
[36] Univ Aix Marseille, Inst Rech Dev, Ecole Hautes Etud Sante Publ, EPV, Marseille, France
[37] Cellule Coordinat Natl Lutte Malad Virus Ebola, Conakry, Guinea
基金
欧盟地平线“2020”;
关键词
HEMORRHAGIC-FEVER; CONVALESCENT PLASMA; T-705; FAVIPIRAVIR; SEVERE SEPSIS; VIRAL LOAD; PATIENT; INFECTION; OUTBREAK; FEATURES; OUTCOMES;
D O I
10.1371/journal.pmed.1001967
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ebola virus disease (EVD) is a highly lethal condition for which no specific treatment has proven efficacy. In September 2014, while the Ebola outbreak was at its peak, the World Health Organization released a short list of drugs suitable for EVD research. Favipiravir, an antiviral developed for the treatment of severe influenza, was one of these. In late 2014, the conditions for starting a randomized Ebola trial were not fulfilled for two reasons. One was the perception that, given the high number of patients presenting simultaneously and the very high mortality rate of the disease, it was ethically unacceptable to allocate patients from within the same family or village to receive or not receive an experimental drug, using a randomization process impossible to understand by very sick patients. The other was that, in the context of rumors and distrust of Ebola treatment centers, using a randomized design at the outset might lead even more patients to refuse to seek care. Therefore, we chose to conduct a multicenter non-randomized trial, in which all patients would receive favipiravir along with standardized care. The objectives of the trial were to test the feasibility and acceptability of an emergency trial in the context of a large Ebola outbreak, and to collect data on the safety and effectiveness of favipiravir in reducing mortality and viral load in patients with EVD. The trial was not aimed at directly informing future guidelines on Ebola treatment but at quickly gathering standardized preliminary data to optimize the design of future studies.
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