Emergent BioSolutions Announces FDA Approval of Change in Storage Conditions and Transfer of Manufacturing for Its Cholera Vaccine
“Emergent is pleased with this
In the U.S., the vaccine is marketed as Vaxchora®. The vaccine is indicated for active immunization against disease caused by Vibrio cholerae serogroup O1. Vaxchora® is approved for use in adults 18 through 64 years of age traveling to cholera-affected areas. Limitations of Use: The effectiveness of Vaxchora® has not been established in persons living in cholera-affected areas. The effectiveness of Vaxchora® has not been established in persons who have pre-existing immunity due to previous exposure to V. cholerae or receipt of a cholera vaccine. Vaxchora® has not been shown to protect against disease caused by V. cholerae serogroup O139 or other non-O1 serogroups. It was approved by the
For full Prescribing Information, please visit www.vaxchora.com.
About Cholera
Cholera, transmitted by ingestion of food and water contaminated with Vibrio cholerae, may present with a broad range of symptoms. Cholera commonly presents as watery diarrhea, but may also be asymptomatic or, in severe cases, characterized by profuse watery diarrhea.i If untreated, these severe cases may lead to dehydration, hypovolemic shock and death within hours.i With limited surveillance capacities, as well as social, economic and political disincentives, cholera is an underreported disease.
About
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This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Any statements, other than statements of historical fact, including statements related to our ability to respond to increased global product demand, maximizing the capacity utilization of our facilities and expansion of our supply chain, customer base and market area, are forward-looking statements. These forward-looking statements are based on our current intentions, beliefs and expectations regarding future events. We cannot guarantee that any forward-looking statement will be accurate. Investors should realize that if underlying assumptions prove inaccurate or unknown risks or uncertainties materialize, actual results could differ materially from our expectations. Investors are, therefore, cautioned not to place undue reliance on any forward-looking statement. Any forward-looking statement speaks only as of the date of this press release, and, except as required by law, we do not undertake to update any forward-looking statement to reflect new information, events or circumstances.
There are a number of important factors that could cause the company's actual results to differ materially from those indicated by such forward-looking statements, including our ability to obtain and maintain regulatory approvals; and our commercialization, marketing and manufacturing capabilities. The foregoing sets forth many, but not all, of the factors that could cause actual results to differ from our expectations in any forward-looking statement. Investors should consider this cautionary statement, as well as the risk factors identified in our periodic reports filed with the
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i Wong KK, Burdette E, and Mintz ED. Cholera.
ii Ali M et al. Updated Global Burden of Cholera in Endemic Countries. 2015; PLoS Negl Trop Dis. 2015
iii WHO (2016) Cholera surveillance and number of cases.
iv Wong KK et al. Recommendations of the advisory committee on immunization practices for use of cholera vaccine. MMWR. 2017; 66 (18): 482-485.
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