Protalix BioTherapeutics, Inc. reported a significant increase in revenue for the fiscal year ending December 31, 2024, generating $53.0 million, a 31% rise from $40.4 million in 2023. This growth was primarily driven by a $11.8 million increase in sales of Elfabrio to Chiesi, alongside modest increases in sales to Brazil and Pfizer. However, revenue from license and R&D services plummeted by 98% to $0.4 million, largely due to the absence of milestone payments following the FDA approval of Elfabrio in May 2023, which had previously contributed $20 million in 2023.

The company’s net income for 2024 was $2.9 million, a decrease from $8.3 million in 2023, attributed to a reduction in revenues from R&D services and increased operational costs. Research and development expenses fell by 24% to $13.0 million, reflecting the completion of the Fabry clinical program. Selling, general, and administrative expenses also decreased by 19% to $12.2 million, indicating a strategic effort to manage costs amid fluctuating revenues.

Operationally, Protalix continues to focus on expanding its product pipeline, which includes PRX-115 for uncontrolled gout and PRX-119 for NETs-related diseases. The company is preparing to initiate a Phase II clinical trial for PRX-115 in the second half of 2025. As of December 31, 2024, Protalix employed 213 individuals, maintaining a stable workforce to support its ongoing projects and operational needs.

Looking ahead, Protalix anticipates continued investment in research and development, with expectations of increased expenses as it advances its clinical trials. The company believes its current cash and cash equivalents, totaling $34.8 million, are sufficient to meet its capital needs for at least the next 12 months. However, it acknowledges the potential need for additional financing to support its growth strategy, particularly as it seeks to expand its product offerings and navigate the complexities of regulatory approvals and market competition.

About Protalix BioTherapeutics, Inc.

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