The hemophilia market is expecting an influx of new products currently at the later stages of clinical development, including gene therapies, that will pile pressure on payers looking to contain costs. To secure market access, it will be critical for companies with entirely novel hemophilia therapies, as well as those providing incremental treatment benefits, to start conversations with payers as soon as possible. Care should also be taken over the design of clinical trials in order to maximize a new product's attractiveness.
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