Leads from the MMWR. Update: influenza activity--United States--and influenza type B virus drift

JAMA ◽  
1986 ◽  
Vol 255 (9) ◽  
pp. 1112-1113
Virology ◽  
1990 ◽  
Vol 175 (1) ◽  
pp. 59-68 ◽  
Author(s):  
Paul A. Rota ◽  
Teresa R. Wallis ◽  
Maurice W. Harmon ◽  
Jennifer S. Rota ◽  
Alan P. Kendal ◽  
...  

1964 ◽  
Vol 79 (1) ◽  
pp. 107-112
Author(s):  
I. J. GREEN ◽  
S. C. HUNG ◽  
P. S. YU ◽  
G. W. LEE ◽  
H. G. PEREIRA

1993 ◽  
Vol 29 (1) ◽  
pp. 21-31 ◽  
Author(s):  
Anaira C. Clavo ◽  
Hunein F. Maassab ◽  
Michael W. Shaw

2018 ◽  
Vol 5 (suppl_1) ◽  
pp. S48-S48
Author(s):  
Keiko Kawaguchi ◽  
Simon Portsmouth ◽  
Takao Shishido ◽  
Takeki Uehara ◽  
Frederick Hayden

Abstract Background Baloxavir marboxil (BXM), a selective cap-dependent endonuclease inhibitor, has demonstrated efficacy + safety for influenza in otherwise healthy patients. We present subgroup analyses for (i) United States vs. Japan (J), (ii) time (t) of treatment (early: ≥0 to ≤24 hours, vs. late: >24 to ≤48 hours), and (iii) influenza type B infections from the global Ph 3 trial (16/17 season). Methods A multicenter, randomized, double-blind, placebo (PLC)- and oseltamivir (OV)-controlled study recruited patients in Japan (n = 846) and United States (n = 590). Inclusion criteria: age 12–64 years, fever + flu symptoms, and ≤48 hours from symptom onset. Patients (20–64 years) randomized (2:2:1) to a single oral dose of BXM, PLC, or 75 mg OV BID for 5 days; patients 12–19 years were randomized (2:1) to receive BXM or PLC. BXM dose: 40/80 mg for BW </≥80 kg. Primary endpoint: time to alleviation of symptoms (TTAS) in ITTI population (pop). Viral titers measured from pre-/postdose nasal swabs. Results BXM reduced the median TTAS by 30.6 hours versus PLC (87.3 versus 117.9 hours, P = 0.1373) in the US pop and t to cessation of viral shedding: 24 versus 72 hours for PLC (P < .0001). Median TTAS in the United States versus J pop was longer, due to imbalances between groups. In both early/late treatments from symptom onset, BXM reduced TTAS versus PLC (Table 1). Regardless of the t to treatment from symptom onset, BXM reduced virus titer significantly from BL versus PLC and OV (Table 2). No significant reduction in TTAS was seen, while BXM reduced virus titer versus PLC and OV in type B virus infection. Conclusion Outcomes for United States were aligned with the Ph 3 Results. Early treatment with BXM leads to a significantly faster TTAS vs. PLC. BXM caused significant viral titer reduction regardless of treatment time versus OV. BXM reduced virus titer vs. PLC and OV in type B virus infection. Disclosures K. Kawaguchi, Shionogi & Co., Ltd.: Employee, Salary. S. Portsmouth, Shionogi Inc: Employee, Salary. T. Shishido, Shionogi & Co., Ltd.: Employee, Salary.T. Uehara, Shionogi & Co., Ltd.: Employee, Salary. F. Hayden, Shionogi & Co., Ltd.: Scientific Advisor, Consulting fee (donated) and travel support for attending 6th ESWI meeting, 10–13 September 2017, Latvia, to present phase 3 OWH results.


2004 ◽  
Vol 19 (1) ◽  
pp. 64-67 ◽  
Author(s):  
Shih-Ming Huang ◽  
Chu-Chin Chen ◽  
Pao-Chin Chiu ◽  
Ming-Fang Cheng ◽  
Ping-Hong Lai ◽  
...  

1993 ◽  
Vol 111 (3) ◽  
pp. 539-546 ◽  
Author(s):  
M. L. Hemphill ◽  
P. A. Rota ◽  
V. T. Ivanova ◽  
A. N. Slepushkin ◽  
A. P. Kendal

SummaryFour influenza type B viruses isolated in Russia during periods of relatively low (1987–8) or high (1990–1) influenza B activity were characterized antigenically using a microneutralization assay. These isolates were antigenically similar to contemporary reference strains from either of two separate lineages represented by B/Victoria/2/87 and B/Yamagata/16/88. The evolutionary relationships of the variable portion of the haemagglutinin (HA1) genes of these viruses were determined by comparison with influenza B HA1 sequences previously obtained. The Isolate B/USSR/2/87, collected during the 1987–8 influenza season, was found to be closely related to viruses on the B/Victoria/2/87 lineage that circulated during the 1988–9 influenza season in the United States. Sequence analysis of the isolates from the 1990–1 influenza season demonstrated co-circulation of viruses from both the B/Victoria/2/87 and B/Yamagata/16/88 lineages in Russia, confirming the antigenic analysis.


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