From a non experts view, if the brain makes the decision, then if the part of the brain which controls this is disabled we will not feel pain. Hence developing a medication that will target the area which controls the pain. However with DDD if you control the pain you still have the problem of mobility.
I do not agree with your concluding comment, while the Phase I is more for safety the FDA will approve only a product if it passes safety and efficacy standards.
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