Arcellx reported a net loss of $47.1 million for Q4 2024, with collaboration revenue decreasing to $15.3 million. The company ended the quarter with $625.7 million in cash, cash equivalents, and marketable securities, projecting a cash runway into 2027. Key clinical highlights include positive preliminary data from the iMMagine-1 study for anito-cel, showing high overall response rates and a manageable safety profile.
Arcellx reported a net loss of $47.1 million for the fourth quarter of 2024.
Collaboration revenue for Q4 2024 was $15.3 million, a decrease from the previous year.
The company ended Q4 2024 with $625.7 million in cash, cash equivalents, and marketable securities.
Positive preliminary data from the Phase 2 pivotal iMMagine-1 study of anito-cel showed a 97% overall response rate and 62% complete response/stringent complete response rate in RRMM patients.
Arcellx anticipates presenting updated data from the iMMagine-1 study mid-year 2025, preparing for the commercial launch of anito-cel in multiple myeloma in 2026, enrolling its program in generalized myasthenia gravis, and expanding its ARC-SparX program.