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Cerus (CERS) investor relations material
Cerus Q1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Q1 2026 total revenue reached $59.9 million, up 23% year-over-year, with product revenue at $53.7 million, driven by strong global platelet and IFC demand.
Net loss narrowed to $1.6 million ($0.01 per share) from $7.7 million ($0.04 per share) year-over-year, reflecting improved operating performance.
Full-year 2026 product revenue guidance raised to $227–$231 million, with IFC revenue guidance increased to $22–$24 million.
North America contributed nearly 70% of Q1 product revenue, with significant gains in platelet kit volumes and treatable doses; EMEA region delivered robust growth, led by France and Belgium, supported by a renewed multi-year contract with the French Blood Establishment.
Leadership transition announced: Vivek Jayaraman to become CEO effective July 2026, with Obi Greenman moving to chairman role.
Financial highlights
Product revenue was $53.7 million, up 24% year-over-year; total revenue, including government contracts, was $59.9 million, up 23%.
Product gross margin declined to 52% from 58.8% due to inflation, tariffs, and prior year one-time benefit.
Operating expenses declined 7% year-over-year to $34.5 million, with R&D expenses down 12% to $14.5 million and SG&A down 2% to $19.9 million.
Non-GAAP adjusted EBITDA improved to $4 million, marking the eighth consecutive positive quarter.
Cash, cash equivalents, and short-term investments totaled $80.4 million at quarter-end; net cash used in operating activities was $3 million.
Outlook and guidance
Full-year product revenue growth expected at 10–12% year-over-year; IFC revenue growth projected at 30–40%.
2026 gross margin anticipated to remain in the low 50s due to persistent inflation, FX, and tariffs.
Third consecutive year of positive adjusted EBITDA expected for 2026.
INT200 U.S. PMA submission planned for Q2 2026, with launch expected in H1 2027; INTERCEPT Red Blood Cell System CE Mark approval targeted for H1 2027, pending regulatory review and study readout.
Expects government contract revenue to decrease as the 2016 BARDA agreement ends in September 2026.
- Record revenue growth and global expansion driven by INTERCEPT blood safety technologies.CERS
Corporate presentation22 Apr 2026 - Proxy covers director elections, equity plan expansion, pay, auditor, and governance highlights.CERS
Proxy filing22 Apr 2026 - Virtual vote set for June 2026 on directors, equity plan, pay, and auditor ratification.CERS
Proxy filing22 Apr 2026 - Record 2025 growth and global expansion highlight strong momentum in blood safety innovation.CERS
Corporate presentation9 Mar 2026 - Double-digit growth driven by U.S. and global expansion, new products, and strong partnerships.CERS
TD Cowen 46th Annual Health Care Conference3 Mar 2026 - 2025 revenue hit $233.8M with narrowing losses and strong IFC and INT200-driven growth.CERS
Q4 20252 Mar 2026 - Q2 product revenue up 16%, net loss narrowed, and 2024 guidance raised to $175–178M.CERS
Q2 20242 Feb 2026 - BARDA awards up to $248M for U.S. program; Europe plans new submission after CE Mark setback.CERS
Study Update19 Jan 2026 - Q3 2024 revenue up 16%, net loss narrowed, and full-year guidance raised on strong demand.CERS
Q3 202417 Jan 2026
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