Silly question: now that we have ph1 complete for MND. Assuming no alteration to formulation of MPL or dosage, could we jump straight to Ph2 for other conditions?
Or do we still need to determine safety specifically for people with a particular condition? Would it depend on the condition per regulatory board adjudication?
The Final Charge , Phase I/II MND Results & FDA ODD Approval Catalyst, page-1077
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