Precision oncology company Repare Therapeutics Inc (Nasdaq: RPTX) announced on Wednesday that it has entered into a definitive asset purchase agreement with Gilead Sciences Inc for the sale of its polymerase theta ATPase inhibitor RP-3467, with total consideration of up to USD30m.
The agreement provides for USD25m in upfront cash to Repare Therapeutics, subject to customary holdbacks and adjustments, and a further USD5 million payment contingent on completion of specified technology transfer activities.
Transaction strengthens Repare Therapeutics' cash position ahead of its previously announced acquisition by XenoTherapeutics, Inc. and Xeno Acquisition Corp., under which Xeno will acquire all outstanding Repare common shares. Shareholder consideration is based on Repare's closing net cash balance after deductions for transaction costs and liabilities.
Proceeds from the Gilead Sciences transaction have increased the estimated closing net cash amount, resulting in an updated expectation that Repare shareholders will receive approximately USD2.20 per common share at closing.
RP-3467 is a small-molecule Polθ inhibitor targeting synthetic lethality associated with BRCA mutations and other genomic alterations and is currently being evaluated in the POLAR Phase 1 clinical trial across multiple advanced solid tumour indications.
Faron launches BLAZE trial with Institute of Cancer Research to address immunotherapy resistance
AstraZeneca secures US Breakthrough status for Enhertu in early breast cancer
Ipsen licenses Simcere Zaiming antibody-drug conjugate for global development
Shield Therapeutics wins FDA approval to expand ACCRUFeR use to adolescents
Hansa Biopharma submits imlifidase Biologics License Application to FDA
T-MAXIMUM Pharmaceutical receives IND approval to start Phase II trial of MT027 for rGBM
Ipsen closes Phase II FALKON trial after missing primary endpoint in FOP
Curasight reports first patient dosed in Phase 1 uTREAT trial in brain cancer
Clywedog Therapeutics activates all clinical centres and patient dosing in balomenib Phase 1b study