Moderna — Jan 13, 2025 release
Fiscal 2024 fourth-quarter results · 8-K Item 2.02 · Exhibit 99.1 · 0001682852-25-000002
Showing in the filing
Additional cash cost savings
“$0.5 billion”
Period
FY2026
Measure
Company-defined measure
Source
Guidance table
All guidance in this release · 11
Expected revenue range for FY2025
“$1.5 to 2.5 billion”
Revenue for FY2025
“$1.5 to 2.5 billion”
Cash cost expenses reduction for FY2025
“$1.0 billion”
Expected ending cash balance for FY2025
“approximately $6.0 billion”
Prioritized programs with anticipated milest…
“10”
Potential product approvals for FY2025
“up to three potential 2025 approvals”
Registrational data readouts
“six”
Product approvals target
“up to 10 product approvals over the next three years”
Additional 2026 cost reductions for FY2026
“$0.5 billion”
Additional cash cost savings for FY2026
“$0.5 billion”
Cost reduction / breakeven target for FY2028
“breakeven in 2028”
Exhibit 99.1 · the passage around this item
… earlier in the release
2025 financial framework: Moderna is accelerating and expanding its previous cost efficiency and prioritization programs and now projects cash cost reductions of $1.0 billion (including cost of sales, research and development, and selling, general & administrative expense) in 2025. The Company expects an additional $0.5 billion in potential cash cost savings in 2026. Moderna now projects $1.5 billion to 2.5 billion in revenue in 2025, mostly in the second half of the year, primarily due to Spikevax and mRESVIA vaccine sales. The Company expects to end 2025 with cash and investments of approximately $6.0 billion. Summary of Late-Stage Pipeline Milestones Respiratory vaccines: • Next-generation COVID-19 vaccine : Moderna shared positive Phase 3 vaccine efficacy and immunogenicity data for its next-generation COVID-19 vaccine (mRNA-1283) at its 2024 R&D Day event. The Company has filed for regulatory approval of mRNA-1283 using a priority review voucher. The FDA has accepted Moderna’s Biologics License Application (BLA) for mRNA-1283 and has assigned a Prescription Drug User Fee Act (PDUFA) goal date of May 31, 2025. • Respiratory syncytial virus (RSV) vaccine : Moderna received regulatory approval of its RSV vaccine mRESVIA (mRNA-1345) for adults aged 60 years and older in 2024. The Company shared positive Phase 3 data for mRNA-1345 in high-risk adults aged 18-59 at its 2024 R&D Day event and has since filed with the FDA for regulatory approval using a priority review voucher . • Seasonal flu/COVID vaccine
later in the release …
the item shown at left
other guidance in this release
Text is the filed exhibit, verbatim.