"The FDA has prevented any trial from being started from about 2020."
Well that's clearly misleading given that the FDA recommended that Mesoblaat conduct at least one randomized well trial in adults or children for aGVHD. It was SI that claimed they had been told they couldn't do another trial until the potency assay was validated. I strongly suspect that applied only to single arm trials
Ann: Mesoblast Corporate Presentation, page-28
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