No silly question when it comes to biotech.
To answer your question the Phase I trial will be an "all comers” trial where patients with any cancer type can be included. This should make the trial recruit relatively fast (you are not looking for a specific cancer type) as well as offer the opportunity to even show efficacy given how frequently FTO is overexpressed in cancer.
I don’t think it would be ethical to give healthy people Bisantrene at this stage even at low doses.
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