Approval of AUCATZYL
AUCATZYL received FDA approval, marking a significant milestone for Autolus Therapeutics and providing a new treatment option for patients with relapsed or refractory ALL.
Launch Readiness and Center Onboarding
60 centers in the U.S. are at various stages of onboarding, with 30 ready for activation, covering 60% of the target patient population. Plans to expand to 90% coverage by adding 30 more centers in 2025.
Strong Financial Position
Cash and cash equivalents totaled $657.1 million as of September 30, 2024, up from $239.6 million at the end of December 2023, supporting commercialization and pipeline plans.
Manufacturing Capacity
The Nucleus manufacturing facility in the U.K. supports a capacity of approximately 2,000 products per year, with a target vein-to-release time of 16 days.
Upcoming Milestones
Key presentations planned for the ASH Annual Meeting, and initial data from the Phase I SLE trial expected by the end of Q1 2025.