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Altimmune Announces Third Quarter 2026 Financial Results and Business Update

  • Altimmune reported $480 million in cash, cash equivalents, and investments as of September 30, 2026.
  • The global PERFORMA Phase 3 trial for MASH is progressing as planned with a 52-week topline readout anticipated in 2029.
  • Positive RECLAIM Phase 2 data for AUD was highlighted in a late-breaking oral presentation at AASLD The Liver Meeting 2026.
  • An End-of-Phase 2 meeting with the FDA for the AUD program is scheduled for December 2026 to discuss the Phase 3 registrational program.
  • Enrollment is complete in the RESTORE Phase 2 trial for ALD, with topline data expected in the second half of 2027.
  • Pemvidutide received Breakthrough Therapy Designation from the FDA for MASH based on 24-week IMPACT Phase 2b data.
  • Research and development expenses were $27.0 million for the three months ended September 30, 2026, driven by the PERFORMA MASH trial and RESTORE ALD trial.
  • Net loss for the three months ended September 30, 2026, was $31.6 million, or $0.15 per share, compared to $19.0 million in the same period in 2025.
  • Peter Greenleaf and Alex Howarth were appointed to the Board of Directors in October 2026 to support strategic evolution.
  • Altimmune relocated its corporate headquarters to Morristown, New Jersey, in November 2026.
Company
Altimmune, Inc
Keywords
Nasdaq:ALT, Altimmune, Inc