ESSA Pharma reported its financial results for the first quarter of fiscal year 2024. The company is focused on advancing masofaniten in combination with antiandrogen agents and is pleased with the data reported from the Phase 1 dose escalation study. ESSA expects its cash position will provide sufficient runway to fund planned operations through data readouts and beyond 2025.
Masofaniten plus enzalutamide continues to be well tolerated with deep and durable reductions in PSA in Phase 1 dose escalation in patients with mCRPC.
81% of patients achieved PSA90, 69% of patients achieved PSA90 in less than 90 days, and 63% of patients achieved PSA <0.2ng/mL.
Phase 2 masofaniten plus enzalutamide combination dose expansion study is ongoing.
Cash runway is sufficient to fund operations beyond 2025.
ESSA Pharma is focused on advancing the investigation of masofaniten in combination with second-generation antiandrogen agents, with the goal of improving clinical outcomes for patients battling prostate cancer. The company expects its cash position will provide sufficient runway to fund planned operations through data readouts and beyond 2025.