The global Soliris market is estimated to be valued at USD 2,080.2 million in 2025 and is expected to reach USD 982.6 million by 2032, exhibiting a compound annual growth rate (CAGR) of -10.2% from 2025 to 2032. The global Soliris market represents a notable segment within the rare disease therapeutics domain, known for pioneering complement inhibition therapy for life-threatening disorders such as paroxysmal nocturnal hemoglobinuria (PNH), atypical hemolytic uremic syndrome (aHUS), and neuromyelitis optica spectrum disorder (NMOSD). Soliris (eculizumab), a monoclonal antibody developed to inhibit complement protein C5, has historically transformed the standard of care in these indications. Its life-saving potential and targeted mechanism of action made it a benchmark in personalized medicine and rare disease management. However, despite its clinical significance, the Soliris market has reached a maturity phase and now faces mounting headwinds, signaling the beginning of a slow decline globally. The increasing availability of biosimilars, cost-containment policies, and a shift toward newer alternatives like Ultomiris are redefining the market outlook, shifting Soliris from a growth driver to a legacy therapy within the competitive pharmaceutical landscape.
Market Dynamics:
The current dynamics of the global Soliris market are shaped by a combination of diminishing growth drivers and intensifying market restraints. While past growth was driven by increased rare disease awareness, better diagnostic tools, and regulatory incentives for orphan drugs, the market is now witnessing stagnation and projected decline through 2032. The negative CAGR is primarily attributed to the expiration of key patents, leading to the global introduction of biosimilar competitors which offer similar therapeutic outcomes at significantly lower prices. This has eroded Soliris's pricing power and market share, especially in cost-sensitive and government-regulated markets.
Further, healthcare systems across Europe, Asia Pacific, and Latin America are tightening reimbursement policies and introducing pricing caps, making it increasingly difficult for Soliris to maintain formulary placement without steep discounts. Clinicians and payers are also shifting preference to newer-generation drugs like Ultomiris, which offer less frequent dosing and lower long-term costs. While opportunities still exist in untapped emerging markets and for off-label indications, these are unlikely to offset the overall revenue decline.
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