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What this means for the PCAC outcome: The committee is unlikely to treat a non-FDA China-based trial as equivalent to a US IND-backed Phase 2 program, but the existence of NCT07437547 represents a material change from the prior PCAC review cycle, when no registered human trials existed

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End-users may either ingest it directly via oral administration or blend it into assorted drinks and daily beverages without pre-dissolving procedures