Here in essence is the typical timeline for Biotech that needs to go all the way from preclinical development into Phase I, Phase II and Phase II trials and then approval.
Bisantrene has over 40 II and III clinical trials - all data that helps RAC accelerate their planned Phase II trials, with possibility of Bisantrene being accelerated to approval for AML under the 505(b)(2) pathway.
This is from a CUV presentation. Clinical studies first started in 2006.
https://www.asx.com.au/asxpdf/20200520/pdf/44hz58ck3dn2gd.pdf
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