GREY:ATBPF - Post by User
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RjM2018on Mar 19, 2021 1:27am
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Post# 32835774
RE:RE:RE:RE:RE:RE:RE:OA & Back pain worth
RE:RE:RE:RE:RE:RE:RE:OA & Back pain worth Solid Post Mugsy.
I agree with you. From a strategic perspective it is now increasingly important to accelarate development of all other candidate molecules. After researching 15+ deals in the rare disease space, the platform play is the way to command more money in case of a buyout.
When consultants perform due diligence reports they build out product profiles to solicit input from KOL on how such a product would impact their prescribing behaviors. Without human data, these reports are based on hypothetical situations and therefore not overly reliable in determining value of the molecule (ie: capture of market share). If you recall back to 346 - it was determined this would be a gold standard product - this was possible was because we had supportive Phase 2 human data to base the product profile on...basically the faster we can gather 352 phase 1 data, the better and perform such DD reports the better.
just a thought.