Release Date: November 07, 2024
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
Q: Can you explain the FDA's substantive review process for your De Novo submission? A: Phillip Chan, CEO: The substantive review is the main process for our De Novo submission. Historically, the FDA's target has been a 150-day review, but post-pandemic, it's been about 11 months. We expect a decision sometime in 2025. Our breakthrough device designation makes us eligible for priority review, which can expedite the process through more interactive and collaborative discussions with the FDA.
Q: Could the FDA approval for Drugsorb A TR happen in the second quarter of 2025? A: Phillip Chan, CEO: We expect approval sometime in 2025, but we cannot predict the exact timelines of the FDA.
Q: Is the Taiwan launch proceeding as planned? A: Phillip Chan, CEO: We recently received regulatory approval in Taiwan and have been working closely with our distributor. We anticipate the launch will accelerate, likely in the next year.
Q: Regarding the $5 million in restricted cash, will it be released in the fourth quarter following the FDA application submission? A: Peter Mariani, CFO: The restriction will be lifted once we raise $5 million in new equity, allowing us to free up $10 million in liquidity.
Q: Can you provide more details on the purified pump program? Is it in a trial phase or will it be marketed extensively? A: Phillip Chan, CEO: The purified pump is designed to expand the use of our therapy in areas lacking dialysis infrastructure. It's user-friendly and encourages early treatment with Cytosorb, which is crucial for good outcomes. It's an enabling technology to drive demand for our cartridges, and while we sell it for profit in some regions, we subsidize it in others to promote cartridge sales.
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
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