the weak link for RAC has always been that it didn’t have a drug in a suitable form to take to the clinic for any condition other than AML.
Reformulating bisantrene into 220 version so it is ready for clinical trials has, and is still taking, forever….
in hindsight, the best way RAC could have spent money might have been to throw everything into speeding up the creation of version 220.
…because no clinically suitable drug means no clinical trials….and ASX-listed biotech that can’t do clinical trials don’t get much pricing respect from investors.
the weak link for RAC has always been that it didn’t have a drug...
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