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AEON Biopharma (AEON) investor relations material
AEON Biopharma Registration Filing summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Company overview and business model
Focuses on developing ABP-450 as a BOTOX® biosimilar for therapeutic indications, targeting accelerated and full-label U.S. market entry via a Biologics License Application under Section 351(k).
Holds exclusive development and distribution rights for ABP-450 in the U.S., Canada, EU, UK, and select international territories.
ABP-450 is manufactured by Daewoong Pharmaceutical in cGMP-compliant, FDA, Health Canada, and EMA-approved facilities.
The global therapeutic botulinum toxin market is estimated at $3.3 billion, based on 2024 Botox segment revenues.
Built a management team with deep experience in biopharmaceutical and botulinum toxin development and commercialization.
Financial performance and metrics
KPMG LLP's audit report notes recurring losses from operations, net capital deficiency, and negative cash flows, raising substantial doubt about the company's ability to continue as a going concern.
Financial statements for 2024 and 2023 are incorporated by reference, with the latest annual report filed March 24, 2025.
Use of proceeds and capital allocation
Will not receive proceeds from the resale of shares by registered holders; proceeds from warrant exercises (if paid in cash) will go to the company.
Registered holders bear underwriting discounts and commissions; company covers registration and related offering expenses.
Next AEON Biopharma earnings date
Next AEON Biopharma earnings date
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