I'm about to go to bed now, but there's something that's been gnoring in my mind...
if during a combination therapy trial, adverse reactions are observed in a participant, how do they work out which drug caused the reaction? I'll probably answer my own question here by saying that we're (IMU) providing a platform to carry the other company's drug and trials to date don't show any adverse effects from our drug as yet, but what if???
Just curious, not overly concerned as I'm not a scientist.
Any thought's anyone?
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