Roughly 90 patients have been treated with Bisantrene via the historic and the Israel trials for AML. At a guess several hundred doses administered for AML. Thousands of doses administered if you include patients treated historically with Bisantrene via trials for solid tumours.
So RACE have a big advantage relating to LILRB4, although this perhaps not known historically as potentially relevant in terms of mechanism of action for AML.
Sounds like FTO is upstream of LILRB4 and from all the data available has a broader application. So FTO is perhaps analogous to a master key.
Immuno-Onc seems to be targeting LILRB4 significantly.
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