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ESSA Pharma Presents Updated Phase 1/2 Masofaniten (EPI-7386) Clinical Data at the 2024 ESMO Congress
ESSA Pharma presented updated Phase 1/2 clinical data for masofaniten (EPI-7386) in combination with enzalutamide at the 2024 ESMO Congress. The study focused on patients with metastatic castration-resistant prostate cancer(mCRPC). Key findings include:
- 88% of patients achieved PSA90
- 69% achieved PSA90 in less than 90 days
- 63% achieved PSA <0.2ng/mL
- After 15.2 months, median time to PSA progression and radiographic progression-free survival not yet reached
- Combination well-tolerated with durable PSA reductions
- Phase 2 dose expansion ongoing at RP2CDs of masofaniten 600 mg BID with enzalutamide 160 mg QD
The data suggests favorable outcomes compared to historical single-agent enzalutamide treatment in mCRPC patients.
- 88% of patients achieved PSA90
- 69% achieved PSA90 in less than 90 days
- 63% achieved PSA <0.2ng/mL
- After 15.2 months, median time to PSA progression and radiographic progression-free survival not yet reached
- Combination well-tolerated with durable PSA reductions
- Phase 2 dose expansion ongoing at RP2CDs of masofaniten 600 mg BID with enzalutamide 160 mg QD
The data suggests favorable outcomes compared to historical single-agent enzalutamide treatment in mCRPC patients.
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