Repurposing bisantrene for AML and solid tumours
No capital raise or buyback data
Australian biotechs with < $20M aggregated turnover can claim a 43.5% refundable tax offseton eligible R&D expenditure each financial year (Jul–Jun). This is paid as a cash refund by the ATO — not a tax deduction — making it non-dilutive capital that directly extends cash runway.
Companies register eligible R&D activities with AusIndustry during the year, then lodge their tax return after 30 June. Refunds typically arrive October–Decemberof the same calendar year. For a company spending $5M/year on R&D, this is a ~$2.2M annual cash inflow.
Peer-reviewed papers & conference abstracts via PubMed
Historical delivery and spending consistency — data is limited for recently added companies.
Outcome quality (positive/negative readouts) reflects the science, not execution — shown above but excluded from the score.
These metrics reflect historical operational data only. They are not predictive of future performance, do not constitute investment advice, and should not be used as the basis for any investment decision.
| Event | Type | Confidence | Impact | Date | Status |
|---|---|---|---|---|---|
| Bisantrene Phase 1/2 AML interim data Initial dose-response data in acute myeloid leukaemia | data readout | Expected | arrow_upwardHigh | 31 May 2026 | Upcoming |
| PHASE1 data readout — A Safety and Pharmacokinetics Study of RC220 Combined With Doxorubicin in Adult open_in_new Primary completion expected for NCT06815575. Indication: {"Solid Tumours","Advanced Solid Tumours"} | data readout | Speculative | removeMed | 31 July 2027 | Upcoming |
| RC220 (E,E-bisantrene) (HARNESS-1) — First Patient Recruited to HARNESS-1 Lung Cancer Trialopen_in_new Racura Oncology has recruited the first patient to its HARNESS-1 Phase 1a/b clinical trial, assessing RC220 in combination with osimertinib in EGFRm NSCLC patients. The first participant was enrolled by Principal Investigator Associate Professor Surein Arulananda and his team at Monash Health in Victoria, Australia. | other | Confirmed | removeMed | 31 Mar 2026 | Completed |
| RC220 (HARNESS-1) — First Patient Recruited to HARNESS-1 Lung Cancer Trialopen_in_new First patient recruited to the HARNESS-1 Phase 1 trial of RC220 in combination with osimertinib for EGFR-mutant NSCLC patients. The trial aims to assess safety, tolerability and pharmacokinetics of RC220 to address resistance to standard-of-care tyrosine kinase inhibitors. | other | Confirmed | removeMed | 31 Mar 2026 |
| Capital raise likely Raised $3.2M placement at $2.83/share (6% premium, Dec 2025) | financing | Confirmed | removeMed | 1 Dec 2025 | Completed |