Release Date: February 12, 2025
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
Q: What is the expected timeline for the European review process for Anavex's Alzheimer's treatment? A: Dr. Christopher Mistling, CEO, stated that the review is expected to take 210 days from the filing, which was accepted in December. They anticipate feedback by the end of the year.
Q: Are there any plans for a priority review for the Alzheimer's treatment? A: Dr. Mistling explained that they filed without prime status due to the unmet need, and thus, a priority review is not applicable.
Q: What upcoming events can stakeholders look forward to? A: Dr. Mistling mentioned the NX 371 schizophrenia readout expected in the first half of the year, a scientific presentation at the ADPD conference in April, and updates on the Parkinson's disease program.
Q: Is there any interest from pharmaceutical companies regarding the Alzheimer's treatment? A: Dr. Mistling confirmed ongoing discussions with pharmaceutical companies and emphasized that they have sufficient supply for launching the drug. The decision on partnerships will focus on maximizing shareholder value.
Q: How significant is the new crystalline patent for Anavex? A: Dr. Mistling highlighted that the crystalline patent is significant as it covers the composition of matter used in all prior clinical studies, providing protection until at least July 2039 for Alzheimer's and Parkinson's disease treatments.
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
This article first appeared on GuruFocus.免責聲明:投資有風險,本文並非投資建議,以上內容不應被視為任何金融產品的購買或出售要約、建議或邀請,作者或其他用戶的任何相關討論、評論或帖子也不應被視為此類內容。本文僅供一般參考,不考慮您的個人投資目標、財務狀況或需求。TTM對信息的準確性和完整性不承擔任何責任或保證,投資者應自行研究並在投資前尋求專業建議。