Do you think patients will have a say? I mean, if they ask for the more convenient formulation.
A small say at most, IMO—I doubt that many MS patients will even know about the new Copaxone option unless they are made aware of it by their neuro.
Moreover, I question whether a 3x per week dosing schedule for a subcutaneous drug is significantly more convenient than a daily one. If the new drug were weekly, that would be a pretty big deal, but thrice-weekly doesn’t gain much in convenience, IMO.
What do you think?
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