Release Date: November 13, 2024
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
Q: Given the brevity of the FDA's requests for narsoplimab, is it reasonable to expect commercial sales in 2025? A: Gregory Demopulos, CEO: Yes, we are targeting 2025 for commercial sales. We plan to quickly resubmit the BLA once we receive and align on the FDA's comments regarding the sensitivity analyses.
Q: Can you provide more details on the phase three trial designs for the MASP-3 inhibitor, particularly for PNH? A: Gregory Demopulos, CEO: The phase three trials will include a switch-over trial for patients not optimally responding to C5 inhibitors and a trial for patients not previously treated with complement inhibitors. Both trials have received positive feedback from FDA and European regulators.
Q: What is your strategy regarding the potential priority review voucher for pediatric C3G? A: Gregory Demopulos, CEO: It's premature to discuss our strategy. We will assess the landscape and decide whether to sell or retain the voucher based on our program's progress and market conditions.
Q: Can you provide an estimate of the size and cost of the OMS 906 phase three program, and will you need a partner to complete it? A: Gregory Demopulos, CEO: We plan to move forward independently, confident in our data and safety profile. The studies will be relatively small, with each trial involving slightly below 100 patients, making them manageable with our current resources.
Q: How will the enrollment process for the OMS 906 trials be managed to ensure timely completion? A: Gregory Demopulos, CEO: We have identified patient pockets and expect to enroll quickly. Our clinical operations team has done significant groundwork to line up patients, which should positively affect the trial's fixed monthly costs.
For the complete transcript of the earnings call, please refer to the full earnings call transcript.
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