scholarly journals Double-Blind Evaluation of Oral Ribavirin (Virazole) in Experimental Influenza A Virus Infection in Volunteers

1977 ◽  
Vol 12 (4) ◽  
pp. 498-502 ◽  
Author(s):  
C. R. Magnussen ◽  
R. G. Douglas ◽  
R. F. Betts ◽  
F. K. Roth ◽  
M. P. Meagher
1998 ◽  
Vol 5 (5) ◽  
pp. 604-608 ◽  
Author(s):  
Deborah Gentile ◽  
William Doyle ◽  
Theresa Whiteside ◽  
Philip Fireman ◽  
Frederick G. Hayden ◽  
...  

ABSTRACT Interleukin-6 (IL-6) is a pleotropic cytokine implicated in the pathogenesis of local inflammation during viral upper respiratory infections. This study determined if experimental influenza A virus infection causes local IL-6 production. Seventeen healthy, adult subjects were intranasally inoculated, by course drops, with a safety-tested strain of influenza A/Kawasaki/86 (H1N1) virus. Nasal lavage samples were collected, symptoms were recorded, and expelled nasal secretions were weighed once before and then daily for 8 days after the virus inoculation. Lavage samples were submitted for virus culture and were examined for IL-6 and IL-4 by enzyme-linked immunosorbent assay. The IL-6, but not IL-4, levels were significantly increased in the nasal lavage samples of the 12 subjects who shed virus but not in those of the 5 subjects who did not shed virus. Moreover, the elevations in IL-6 levels were related temporally to the development of nasal symptoms and secretions but not to systemic symptoms. These results suggest a role for locally produced IL-6 in the pathogenesis and expressed symptomatology of influenza A virus infection.


2011 ◽  
Vol 24 (4) ◽  
pp. 321-330 ◽  
Author(s):  
Nadine Wiesener ◽  
Tatjana Schütze ◽  
Sara Lapp ◽  
Melissa Lehmann ◽  
Nadine Jarasch-Althof ◽  
...  

1999 ◽  
Vol 180 (3) ◽  
pp. 586-593 ◽  
Author(s):  
R. Scott Fritz ◽  
Frederick G. Hayden ◽  
David P. Calfee ◽  
Lindsey M. R. Cass ◽  
Amy W. Peng ◽  
...  

2000 ◽  
Vol 27 (4) ◽  
pp. 323-326 ◽  
Author(s):  
William J Doyle ◽  
James T Seroky ◽  
Betty L Angelini ◽  
Mehmet Gulhan ◽  
David P Skoner ◽  
...  

1996 ◽  
Vol 38 (2) ◽  
pp. 143-153 ◽  
Author(s):  
David P. Skoner ◽  
Betty L. Angelini ◽  
Amy Jones ◽  
James Seroky ◽  
William J. Doyle ◽  
...  

1986 ◽  
Vol 18 (1) ◽  
pp. 119-129 ◽  
Author(s):  
W. Al-Nakib ◽  
P. G. Higgins ◽  
J. Willman ◽  
D. A. J. Tyrrell ◽  
D. L. Swallow ◽  
...  

2020 ◽  
Vol 64 (7) ◽  
Author(s):  
Jeremy J. Lim ◽  
Anna C. Nilsson ◽  
Michael Silverman ◽  
Nimer Assy ◽  
Priya Kulkarni ◽  
...  

ABSTRACT For patients hospitalized with severe influenza A virus infection, morbidity and mortality remain high. MHAA4549A, a human monoclonal antibody targeting the influenza A virus hemagglutinin stalk, has demonstrated pharmacological activity in animal studies and in a human influenza A challenge study. We evaluated the safety and efficacy of MHAA4549A plus oseltamivir against influenza A virus infection in hospitalized patients. The CRANE trial was a phase 2b randomized, double-blind, placebo-controlled study of single intravenous (i.v.) doses of placebo, 3,600 mg MHAA4549A, or 8,400 mg MHAA4549A each combined with oral oseltamivir (+OTV) in patients hospitalized with severe influenza A virus infection. Patients, enrolled across 68 clinical sites in 18 countries, were randomized 1:1:1. The primary outcome was the median time to normalization of respiratory function, defined as the time to removal of supplemental oxygen support to maintain a stable oxygen saturation (SpO2) of ≥95%. Safety, pharmacokinetics, and effects on influenza viral load were also assessed. One hundred sixty-six patients were randomized and analyzed during a preplanned interim analysis. Compared to placebo+OTV, MHAA4549A+OTV did not significantly reduce the time to normalization of respiratory function (placebo+OTV, 4.28 days; 3,600 mg MHAA4549A+OTV, 2.78 days; 8,400 mg MHAA4549A+OTV, 2.65 days), nor did it improve other secondary clinical outcomes. Adverse event frequency was balanced across cohorts. MHAA4549A+OTV did not further reduce viral load versus placebo+OTV. In hospitalized patients with influenza A virus infection, MHAA4549A did not improve clinical outcomes over OTV alone. Variability in patient removal from oxygen supplementation limited the utility of the primary endpoint. Validated endpoints are needed to assess novel treatments for severe influenza A virus infection. (This study has been registered at ClinicalTrials.gov under registration no. NCT02293863.)


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