uniQure(US:QURE) 智通财经网·2025-09-26 08:44Core Insights - Goldman Sachs' analysis highlights the breakthrough progress and commercial prospects of uniQure NV's gene therapy AMT-130 for Huntington's disease, showing significant efficacy in clinical trials [1][2] - The therapy demonstrated a 75% reduction in disease progression and a 60% reduction in total functional ability score changes in the high-dose group after 36 months [1] - The FDA has recognized the manufacturing process validation pathway, and uniQure plans to submit a Biologics License Application (BLA) in Q1 2026 [1][2] Clinical Efficacy - In the high-dose group, 17 patients showed a 75% slowdown in disease progression according to the composite Huntington's disease rating scale, while the low-dose group of 12 patients exhibited a similar trend [1] - Biomarkers and several secondary endpoints support the neuroprotective effect of AMT-130 [1] Safety Profile - Since December 2022, no new serious adverse events have been reported, and all drug-related adverse reactions have been resolved [2] - In a third cohort trial with an immunosuppressive regimen, three serious adverse events fully recovered through supportive care [2] Commercial Outlook - Goldman Sachs projects a peak global sales potential of $2.5 billion for AMT-130, with a 90% probability of success [2] - uniQure plans to initially target approximately 6,000 symptomatic patients out of 20,000 diagnosed in the U.S., assuming a cumulative penetration rate of about 25% [2] - The company will hold a pre-BLA meeting with the FDA in Q4 2025 to discuss confirmatory study requirements and post-marketing research plans [2] Regulatory Strategy - The analysis emphasizes that AMT-130 not only achieves statistical significance in efficacy data but also has an FDA-recognized strategy for accelerated BLA submission [2] - Continuous communication with regulatory agencies and rigorous clinical data accumulation are key to advancing the commercialization of this innovative therapy [2]