Emergent BioSolutions to Acquire ACAM2000® Business From Sanofi
- Addition of ACAM2000®, the only
FDA -licensed smallpox vaccine, expands and diversifies Emergent’s portfolio of medical countermeasures and is synergistic with company’s existing smallpox countermeasure offering - Company to assume responsibility for existing CDC contract with a remaining value of up to approximately
$160 million for deliveries of ACAM2000 to the Strategic National Stockpile - All-cash consideration of
$97.5 million upfront and up to$27.5 million in near-term contingent regulatory and manufacturing-related milestones - Transaction expected to be accretive beginning with anticipated product deliveries in 2018 following
FDA licensure of U.S.-based manufacturing facility
Upon the closing of this transaction, Emergent will acquire:
- ACAM2000®, (Smallpox (Vaccinia) Vaccine, Live), the only vaccine licensed by the
Food and Drug Administration (FDA ) for active immunization against smallpox disease for persons determined to be at high risk for smallpox infection; - An existing 10-year contract originally valued at up to
$425 million with theCenters for Disease Control and Prevention (CDC) with a remaining value of up to approximately$160 million for deliveries of ACAM2000 to the Strategic National Stockpile (SNS); - A cGMP bulk manufacturing facility and a lease to a cGMP fill/finish facility, both U.S.-based, along with the existing staff of approximately 100 employees.
Strategic Rationale
This transaction supports Emergent’s plan to grow through the acquisition of revenue-generating products and businesses, leverages its core competencies in manufacturing and government contracting, and reinforces the company’s strategic focus on providing preparedness solutions for public health threats. The addition of ACAM2000 expands the company’s portfolio of only-in-class products, diversifies its portfolio of medical countermeasures against Category A bioterrorism agents, and is synergistic with its existing smallpox countermeasure offering, specifically VIGIV [Vaccinia Immune Globulin Intravenous (Human)], the only
Upon the closing of the transaction, Emergent will assume responsibility for an existing 10-year CDC contract, which will expire and be up for renewal or extension in 2018. The original contract, valued at up to
Emergent expects that this transaction will enhance its contract manufacturing operations through the addition of live viral manufacturing and fill/finish capabilities and the execution of a contract manufacturing agreement to supply bulk drug substance for one of Sanofi’s commercial vaccines.
This transaction, which is subject to customary closing conditions including antitrust regulatory approval, is expected to close in 2017.
Cowen is acting as financial advisor to Emergent in this transaction.
About ACAM2000
ACAM2000 is the primary smallpox vaccine designated for use in a bioterrorism emergency, with more than 230 million doses having been supplied to the U.S. Strategic National Stockpile. ACAM2000 is also licensed in
About Smallpox
Smallpox is a highly contagious disease caused by the variola virus, a member of the Orthopox virus family. According to the CDC, it is one of the most devastating diseases with a mortality rate as high as 30%. Smallpox is classified by the CDC as a Category A bioterrorism agent and the U.S. government continues to invest in countermeasures to protect the nation from this threat. Governments around the world are also taking precautionary measures to be ready to deal with a potential smallpox outbreak.
Conference Call and Webcast
Emergent will host a conference call to discuss this acquisition on
A replay of the conference call will be accessible approximately one hour following the conclusion of the call by dialing 1.855.859.2056 and using the passcode 24783897. The replay will be available through
About
Safe Harbor Statement
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 regarding the expected closing of the transaction, expected
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 uncertainties as to the satisfaction of closing conditions with respect to the transaction, including the timing and receipt of third-party and regulatory approvals; our ability to successfully integrate the business and realize the benefits of the transaction; the timing of expected
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
Investor Contact:Robert G. Burrows Vice President, Investor Relations 240-631-3280 BurrowsR@ebsi.com Media Contact:Lynn Kieffer Vice President, Corporate Communications 240-631-3391 KiefferL@ebsi.com