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Ben,
Your comments regarding IMU jumping through hoops by combining with approved drugs such as Keytruda and Opdivo, leads me to ask why IMU has planned a PH2 MAST trial for next year?
Looking at the May Newsletter and also at the most recent company presentation it appears to me that IMU are really driving home the point that IMU will be partnering with anybody and everbody who has an approved or soon developing technology that will work synergistically with CF33.
Perhaps the PH2 trial is intending to get approval for CF33 as an adjuvant for cancer therapy . A pre-treatment for Metastatic Advanced Solid Tumors. Then the patient gets treated 2 weeks later with any approved therapy that the Oncologist chooses. ( Keytruda , Opdivo , Tencentic, Blincyto etc)
Is that even an FDA pathway. Because by the time IMU finishes the PH2 trials well over 200 hundred patients will have been treated showing a very good safety profile.
That would put Vaxinia out there as part of a SOC. And Oncarlytics can go on for approvals as a designated therapy.
The attavhed photos show the newsletter talking about opening up the $500bn market to Solid Tumor treatments and all list of all the companies who might want to use CF33.
This s my take on the message that IMU is hammering hom
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