ADMA Biologics delivered a strong third quarter in 2025, with total revenue increasing by 12% year-over-year to $134.2 million and adjusted EBITDA surging by 29% to $58.7 million. The company achieved a pivotal milestone with FDA lot release of its first yield-enhanced production batches, positioning for significant gross margin expansion. Record demand for ASCENIV and progress in its SG-001 pipeline further underscore a positive growth trajectory.
Total revenue for Q3 2025 reached $134.2 million, marking a 12% increase year-over-year, driven by strong ASCENIV adoption.
Adjusted EBITDA grew by 29% year-over-year to $58.7 million, reflecting improved operational efficiencies and a favorable product mix.
The FDA lot release of the first yield-enhanced production batches is a significant operational milestone, expected to accelerate gross margin expansion from Q4 2025 onwards.
Record ASCENIV demand and positive real-world health outcomes data, coupled with advancing payer negotiations, support sustained and accelerating revenue growth.
ADMA Biologics has raised its full-year 2025 and 2026 total revenue guidance, reaffirmed and raised adjusted EBITDA guidance, and revised adjusted net income guidance to reflect a higher effective tax rate. The company projects total annual revenue to exceed $1.1 billion in FY 2029, with anticipated outsized earnings growth.