We are figuratively being held hostage by our 3rd party CDMO. Until the GMP passes specification testing we are stuck in limbo. There is no blame on the BOD from me for this.
So, what are peoples thoughts on the mc valuation if/when we pass and have a successful ph1 trial? I'm thinking $500m.
Ann: Further update on PAT-DX1 GMP manufacturing run, page-51
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