Release Date: February 26, 2025
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
Q: Could you provide a status update on the MIRROR study and its implications for PYLARIFY? Is the timing still on track? A: The MIRROR study is assessing the use of PSMA PET with PYLARIFY in intermediate favorable settings. It continues to enroll, and we expect the last patient in by the fourth quarter of 2025. This study aims to influence guidelines and expand the addressable market for staging populations, potentially increasing from 145,000 to 175,000 scans annually by the end of the decade. - Paul Blanchfield, President
Q: With the new reimbursement changes effective January 1, how are the competitive dynamics in the US PSMA PET market affecting PYLARIFY? A: The new reimbursement code is beneficial for PYLARIFY, and we have secured multiyear contracts with the majority of our customers. Despite competitive pressures, PYLARIFY's clinical and commercial differentiation, including its longer half-life and broad payer access, supports its market leadership and pricing premium. - Brian Markison, CEO; Paul Blanchfield, President; Amanda Morgan, Chief Commercial Officer
Q: Can you discuss the potential for CMS to adopt an ASP-based methodology for PYLARIFY and its impact on growth? A: CMS may establish ASP-based payment rules by January 2026, with draft rules expected in July. If adopted, ASP would support the payment dynamics of PSMA PET diagnostics, potentially enhancing PYLARIFY's growth. Our guidance for 2025 is based on the current MUC payment structure. - Brian Markison, CEO; Paul Blanchfield, President
Q: What are your broader ex-US commercial plans for pipeline assets, especially with the addition of Neuroseq? A: While our focus remains US-based, the acquisition of Life Molecular Imaging and Neuroseq will strengthen our international footprint. We aim to explore opportunities in other markets, particularly the EU, but will proceed cautiously without significant upfront investments. - Brian Markison, CEO
Q: How are you building the data set to highlight the competitive differentiation for MK-6240 and NAV-4694? A: MK-6240 has shown significant advantages in detecting early tau tangles and is involved in over 100 clinical trials. It is recognized as an extraordinary asset, with partnerships in place with major pharma companies. NAV-4694 is shaping up similarly, with potential sensitivity advantages over blood tests. - Brian Markison, CEO
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
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