Release Date: August 08, 2024
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
Q: Assuming positive results from the Phase 2b quality study, how soon can you advance the candidate to the next step, and do you plan to find a partnership for a potential registration study? A: Assuming positive results, we expect to have the Phase 2b quality clinical trial data by January 2025. This data will allow us to engage with the FDA and potential partners. We have already initiated discussions with major players, and having real data will enable more concrete discussions on regulatory and partnership fronts.
Q: In the trials referenced with enobosarm, the high dose was 3 milligrams. What gives you confidence that the 6-milligram dose will be safe, especially considering liver health? A: We have conducted studies with doses as high as 100 milligrams and have data from nearly 250 patients at 9 and 18 milligrams in our breast cancer program, with no evidence of liver toxicity. Additionally, enobosarm has shown a 30% reduction in triglycerides, which may benefit patients with fatty liver. We monitor alcohol intake during the study but do not exclude it.
Q: Can you discuss the progress of the Phase 2b study now that it's fully enrolled, and should we expect any updates before the top-line results in January? A: The study is fully enrolled, and the last patient is expected to complete the study in December. The next update will be the top-line data in January. We are pleased with the safety profile so far, although many patients are still early in their treatment.
Q: What can we expect in terms of top-line data in January? Will it include details on body weight loss, fat loss, and functional improvements? A: The top-line data will focus on body composition, specifically lean body mass and total fat mass, to determine the optimal dose for muscle preservation and fat reduction. Additional details may be shared at scientific meetings shortly after the initial data release.
Q: Regarding the Phase 3 study, will it focus on elderly patients or a broader obesity population? A: The FDA has indicated that a muscle preservation drug could benefit all patients with obesity or overweight, not just the elderly. The Phase 3 study will likely include all comers, with a focus on body weight as the primary endpoint and functional endpoints as key secondary measures. The study will be powered to assess outcomes in both the overall population and a subgroup of older patients.
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
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