You wrote“ The distinction is yet another complicating matter for Clarity (a job for the Clinical/Scientific Advisors): Even COBRA included some of these same men, who were negative SOC - meaning that, if 64Cu-SAR-bisPSMA had been used instead, perhaps it would have detected cancer lesions in some of the same men that ended up included in SABRE (on accould of negative SOC, including 18F-DCFPyL or 68Ga-PSMA-11 scans).”
If they scanned first with Cu64 SAR-bisPSMA, the difference with Bombesin could appear far less superior than it did with 18F-DCFPyL or 68Ga-PSMA-11 scans ( the poorer SOC the better our Bombesin appears).
If FDA saw our CLARIFY, AMPLIFY, SABRE and Head-to-head (when completed and positive) results they cannot but suggest that the guidelines be changed to Cu64 PSMA followed by Cu64 Bombesin for the best identification of most lesions.
Also, for the lesions identified by Cu64 PSMA and Cu64 Bombesin treat with their respective counterpart Cu67 could be logical? So our BOD would be looking to complete these trials for pairing them?
AIMO
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clarity pharmaceuticals ltd
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Ann: SABRE topline results, page-39
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