Long-term growth will hinge on label expansion into WHO FC II patients, sustained hospital adoption, and manufacturer-sponsored patient-assistance programs that preserve access as reimbursement tightens; expect volume CAGR of 4–5% through 2030, well below historical double-digit rates. Innovation is largely incremental—next-gen room-temperature-stable formulations and implantable delivery systems are 3–5 years away, leaving little near-term disruption. Supply is stable, with dual API sourcing and redundancy in sterilization capacity; however, any FDA citation of the sole fill-finish partner would create a 4–6 month shortage, representing the single most material risk beyond faster-than-expected generic erosion.