Autolus posted a Q4 net loss of $27.6 million with $29,000 in revenue and an EPS of -0.09. The quarter reflected ongoing investments into commercialization and pipeline development ahead of broader regulatory milestones.
Autolus Therapeutics reported a net loss of $82.1 million for the third quarter ended September 30, 2024. The FDA approved AUCATZYL, triggering a $30 million milestone payment from Blackstone. The company's cash and cash equivalents totaled $657.1 million.
Autolus Therapeutics reported a net loss of $58.3 million for the second quarter of 2024, compared to a net loss of $45.6 million for the same period in 2023. Cash and cash equivalents totaled $705.9 million as of June 30, 2024. The company is focused on commercial readiness activities for obecabtagene autoleucel (obe-cel).
Autolus Therapeutics reported a net loss of $52.7 million for Q1 2024, compared to a net loss of $39.8 million for the same period in 2023. Cash and cash equivalents totaled $758.5 million as of March 31, 2024, compared to $239.6 million as of December 31, 2023. The company is advancing its obe-cel program and other pipeline developments, supported by recent financing and strategic collaborations.
Autolus Therapeutics reported a net loss of $208.4 million for the year ended December 31, 2023, with cash and cash equivalents totaling $239.6 million. The company highlighted its strategic alliance with BioNTech and the submission of the BLA for obecabtagene autoleucel (obe-cel) to the FDA.