I don't think the composite endpoint trial will have a survival endpoint. They seem to believe they can design a composite as a hard endpoint (i.e. not Subpart H) approval. They plan to do a survival trial, but it won't be the one that starts 2H-2011.
Unless otherwise indicated, this is the personal viewpoint of David Miller and not necessarily that of Biotech Stock Research, LLC. We're on Twitter at BiotechStockRsr