Author's buy case for Race Oncology (RAC) rests on reformulated bisantrene (e,e-bisantrene) acting as the only clinical-stage Myc inhibitor, already clinically derisked by prior AML approval, with multiple expansion catalysts and buyout potential.
RAC.AX — LONG The author bought Race Oncology because its reformulated e,e-bisantrene was found to work via Myc inhibition through G4 binding, making it effectively the only Myc inhibitor in the clinical pipeline, and the prior approved use of bisantrene for AML significantly de-risks safety. Stated catalysts include a current phase 3 bridging study in AML with FDA orphan drug designation, early ctDNA/RNA-based clinical validation of Myc inhibition possibly from existing trial data, a just-starting non-small cell lung cancer trial, and potential use as a cardioprotective alongside chemo or with tyrosine kinase inhibitors to prevent TKI resistance. The investment thesis is a bidding war among big pharmas facing patent expiries, supported by the CEO being the largest shareholder and recently buying on market, with Merck's ~US$32bn approach for Revolution Medicines cited as a valuation comparable. The author notes the company may be circumspect about validation data because it does not yet have composition of matter patents.
The reason I bought in is because the mechanism of action was revealed to be Myc inhibition through G4 binding.