PYC pyc therapeutics limited

same - wonder what changed since AGMDid the FDA spot missing Rat...

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    same - wonder what changed since AGM

    Did the FDA spot missing Rat tox data being incomplete?

    there’s a clearly defined project/protocol checklist for small clinical studies; let alone an IND submission for a clinical trial - it’s done early part in the design process

    we don’t seem to have much rigour in our approach, which is a bit of worry…
 
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