Published in AIDS Weekly, November 17th, 2008
II study with IMVAMUNE(R) in HIV infected subjects that confirms the excellent safety profile of IMVAMUNE(R). Within the next few days the safety report of this study will be submitted to the FDA and this will trigger a USD
25 million milestone payment under the RFP-3 contract. The clinical safety report constitutes a major part of the data package that will be used to potentially support the use of IMVAMUNE(R) in a declared emergency.
In support of using IMVAMUNE(R) as a smallpox vaccine in individuals otherwise contraindicated to receive conventional...
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Source: AIDS Weekly (2008-11-17)
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