Despite the upbeat tempo and confidence, there are serious risks lurking in the background. No 1 has to be the FDA's assessment of the validity of the potency assay. No. 2 is that it's very unlikely that approval for treatment of aGVHD will be given until a successful adult trial that meets the FDA's requirements is completed and No. 3 is funding.
Ann: CEO Presentation to 2023 Annual General Meeting, page-14
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