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Harrow Announces Fourth-Quarter and Year-End 2024 Audited Financial Results

In This Article:

HROW 4Q24 Letter to Stockholders
HROW 4Q24 Letter to Stockholders

Fourth-Quarter, Full-Year 2024, and Recent Highlights:

  • Record revenues of $66.8 million for Q4 2024, an 84% increase over Q4 2023

  • Revenues of $199.6 million for FY 2024, a 53% increase over FY 2023

  • GAAP net income of $6.8 million for Q4 2024, for a GAAP net loss of $(17.5) million for FY 2024

  • Adjusted EBITDA of $22.5 million for Q4 2024, leading to Adjusted EBITDA of $40.3 million for FY 2024

  • IHEEZO® unit demand and VEVYE® prescriptions for Q4 2024 each increased over 40% over Q3 2024

  • VEVYE® Access for All program expected to drive continued market share expansion in 2025

  • TRIESENCE® transitional pass-through approved, significantly increasing addressable market opportunity

NASHVILLE, Tenn., March 27, 2025--(BUSINESS WIRE)--Harrow (Nasdaq: HROW), a leading North American eyecare pharmaceutical company, announced results for the fourth quarter and year ended December 31, 2024. The Company also posted its fourth quarter Letter to Stockholders and corporate presentation to the "Investors" section of its website, harrow.com. The Company encourages all Harrow stockholders to review these documents, which provide additional details concerning the historical quarterly period and future expectations for the business.

"Our stellar fourth-quarter performance, including an 84% year-over-year increase in revenues to a record $66.8 million, marked the end of a monumental year for Harrow, with 2024 revenues rising 53% over 2023 to $199.6 million," said Mark L. Baum, Chief Executive Officer of Harrow. "This strong finish, driven by over 40% quarter-over-quarter growth in both IHEEZO unit demand and VEVYE prescriptions, showcases market uptake for our expanding portfolio and the overall success of the Harrow team. We expect our momentum to continue in 2025, particularly in the second half, as the recently announced VEVYE Access for All program gains traction – accelerating market share capture, expanding commercially covered prescriptions, and bolstering prescriber confidence by ensuring their patients can affordably start treatment with VEVYE, regardless of insurance status. Meanwhile, in addition to our success in stabilizing the supply chain for TRIESENCE, the Centers for Medicare & Medicaid Services recently approved our transitional pass-through application, significantly increasing its addressable market. This terrific news should add fuel to our commercial efforts concurrent with our development of a next-generation version of this high-value and high-trust product. Because we remain at the initial stages of market penetration for our core products, we expect revenue growth in these cornerstone products for years to come."