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Sep 30, 2024

Autolus Q3 2024 Earnings Report

Autolus reported its Q3 2024 financial results and business updates.

Key Takeaways

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.

AUCATZYL (obecabtagene autoleucel) was approved by the US FDA on November 8, 2024.

BLA approval triggered a $30 million milestone payment to Autolus from Blackstone.

Matthias Will M.D. was appointed as Chief Development Officer, effective September 30, 2024.

Obe-cel is under regulatory review in both the EU and the UK.

Total Revenue
$0
Previous year: $406K
-100.0%
EPS
-$0.31
Previous year: -$0.26
+19.2%
R&D expenses
$40.3M
SG&A expenses
$27.3M
Gross Profit
-$223K
Previous year: -$973K
-77.1%
Cash and Equivalents
$657M
Previous year: $257M
+155.8%
Free Cash Flow
-$86.3M
Previous year: -$41.7M
+107.1%
Total Assets
$827M
Previous year: $406M
+103.8%

Autolus

Autolus

Forward Guidance

Autolus anticipates several milestones in the near term. Obe-cel FELIX data will be presented at the American Society of Hematology (ASH) meeting in December 2024. Initial data from the SLE Phase 1 study is expected in Q1 2025 and initial data from the PY01 trial of obe-cel in pediatric ALL is expected in H2 2025.

Positive Outlook

  • Obe-cel FELIX data at American Society of Hematology (ASH) meeting December 2024
  • Obe-cel in autoimmune disease – initial data from SLE Phase 1 study Q1 2025
  • Initial data from PY01 trial of obe-cel in pediatric ALL H2 2025
  • SLE Phase 1 trial presentation at medical conference H2 2025