Question · H2 2025
Steve Wheen asked why the European market for Illuccix and Gozellix is not expected to be a significant growth driver for Telix in the next 12 months, despite product approvals, and also inquired about the shelf life of expensed R&D inventory (cakes) and its potential P&L impact upon FDA approval.
Answer
Christian Behrenbruch, CEO and Managing Director of Telix Pharmaceuticals, explained that European reimbursement processes are lengthy (9-12 months post-approval) and product-specific, delaying material sales. Kevin Richardson, CEO of the Precision Medicine Business, added that 2025 focused on gaining market access, with 2026 now pivoting to execution. Christian also confirmed that the shelf life of expensed R&D inventory extends beyond launch, and it is expected to be backed out of the P&L upon FDA approval.
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