ALX Oncology announced topline data from its ASPEN-06 Phase 2 trial, showcasing evorpacept as the first CD47-blocking agent with durable clinical benefit and a well-tolerated safety profile in a randomized clinical trial. The company reported cash, cash equivalents, and investments of $162.6 million as of September 30, 2024, sufficient to fund planned operations well into Q1 2026.
Reported topline data from the ASPEN-06 Phase 2 clinical trial, demonstrating evorpacept's durable clinical benefit and safety profile in HER2-positive gastric/GEJ cancer patients.
Commenced patient dosing in the Sanofi-partnered arm of the UMBRELLA phase 1/2 clinical study, investigating evorpacept plus SARCLISA and dexamethasone in relapsed or refractory multiple myeloma patients.
Appointed Alan Sandler, M.D. to Board of Directors, bringing over 30 years of oncology and drug development experience.
Cash, cash equivalents and investments as of September 30, 2024, were $162.6 million.
Upcoming clinical milestones for Evorpacept's development pipeline include data presentations and trial initiations across various cancer indications.