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AEON Biopharma (AEON) investor relations material
AEON Biopharma Q2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Strategic shift to a Section 351(k) biosimilar pathway for ABP-450, targeting all current and future therapeutic indications using Botox as the reference product, after discontinuing Phase 2 migraine trials to preserve cash.
Progressed toward key biosimilar milestones, including primary structure and functional analyses for ABP-450, with results expected in Q3 2025 and a Type 2a FDA meeting anticipated in Q4 2025.
Completed public offering in January 2025, raising $18.3 million, and entered into a $15 million convertible note agreement with Daewoong to support late-stage development and working capital.
Appointed Robert Bancroft as CEO in April 2025 following the resignation of the previous CEO.
ABP-450 is already approved as a biosimilar in India, Mexico, and the Philippines.
Financial highlights
Net loss for Q2 2025 was $6.6 million, compared to net income of $164.1 million in Q2 2024, primarily due to non-recurring gains in the prior year.
Cash and cash equivalents totaled $8.4 million as of June 30, 2025, expected to fund operations through Q4 2025 and the planned FDA meeting.
Operating expenses for Q2 2025 were $4.3 million, with SG&A at $3.3 million and R&D at $1.1 million, reflecting a 75% year-over-year decrease in R&D due to trial wind-down.
Stockholders' deficit improved to $(15.9) million at June 30, 2025, from $(28.6) million at December 31, 2024.
Convertible notes at fair value totaled $15.2 million as of June 30, 2025, up from $11.7 million at year-end 2024.
Outlook and guidance
Sufficient cash to fund operations into Q4 2025; additional funding required for further development and to meet obligations beyond that period.
Analytical studies for biosimilar development underway, with results expected in Q3 2025 and an FDA BPD Type 2a meeting planned for Q4 2025.
No revenue expected until regulatory approval and commercialization of ABP-450.
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