Evolus Projects FDA Nod For Evolysse Gels Within 90 Days, Eyes Q2 2025 U.S. Rollout; Reports $79M Q4 2024 Revenue, FY24 Revenue $266.3M; Expects $345M-$355M Net Revenue And $230M-$240M Non-GAAP Expenses For 2025; Plans 8-10% Revenue From Evolysse, Estyme Gels

Benzinga
21 Jan

Expects U.S. Approval Within 90 Days for Evolysse™ Form and Evolysse™ Smooth Injectable Hyaluronic Acid Gels

Provides 2025 Guidance and Maintains Projection for Full-Year 2025 Profitability1

  • Preliminary Unaudited Net Revenue of $79.0 Million for the Fourth Quarter 2024, Representing 30% Growth Over the Prior Year
  • Preliminary Unaudited Net Revenue of $266.3 Million for the Full-Year 2024, Representing 32% Growth Over the Prior Year and at the Top of the Company's Guidance
  • Expects U.S. Food and Drug Administration (FDA) Approval Within 90 Days for Evolysse™ Form and Evolysse™ Smooth Injectable Hyaluronic Acid (HA) Gels; U.S. Launch Planned for Q2 2025, A Full Quarter Ahead of Prior Timeline
  • 2025 Net Revenue Guidance of $345 Million to $355 Million, Which Represents 30% to 33% Growth from Preliminary 2024 Results; Evolysse™ and Estyme® Injectable HA Gels Anticipated to Contribute 8-10% of Total Revenue for the Full-Year 2025
  • 2025 Non-GAAP Operating Expenses Expected to be $230 Million to $240 Million, with Expected Profitability1 for the Full-Year 2025

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