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Date | Price Target | Rating | Analyst |
---|---|---|---|
4/1/2025 | $38.00 | Buy | Chardan Capital Markets |
12/10/2024 | Outperform → Strong Buy | Raymond James | |
10/10/2024 | $20.00 | Outperform | Raymond James |
2/29/2024 | $8.00 | Buy → Neutral | Goldman |
12/19/2023 | $52.00 → $10.00 | Buy → Neutral | Mizuho |
3/17/2022 | $40.00 | Neutral → Buy | UBS |
12/17/2021 | $75.00 → $58.00 | Strong Buy → Outperform | Raymond James |
10/27/2021 | $66.00 | Outperform | William Blair |
Chardan Capital Markets resumed coverage of uniQure with a rating of Buy and set a new price target of $38.00
Raymond James upgraded uniQure from Outperform to Strong Buy
Raymond James resumed coverage of uniQure with a rating of Outperform and set a new price target of $20.00
8-K - uniQure N.V. (0001590560) (Filer)
8-K - uniQure N.V. (0001590560) (Filer)
SCHEDULE 13G - uniQure N.V. (0001590560) (Subject)
4 - uniQure N.V. (0001590560) (Issuer)
4 - uniQure N.V. (0001590560) (Issuer)
4 - uniQure N.V. (0001590560) (Issuer)
~ Proven biotech executive to lead commercialization of AMT-130 in Huntington's disease ~ LEXINGTON, Mass. and AMSTERDAM, June 11, 2025 (GLOBE NEWSWIRE) -- uniQure N.V. (NASDAQ:QURE), a leading gene therapy company advancing transformative therapies for patients with severe medical needs, today announced the appointment of Kylie O'Keefe as Chief Customer and Strategy Officer, effective June 6, 2025. In this role, Ms. O'Keefe will lead the development and execution of uniQure's global commercialization strategy for AMT-130, the Company's investigational gene therapy for the treatment of Huntington's disease. Her responsibilities include all commercial functions and medical affairs. Ms. O'K
~ Alignment with FDA continues to support Accelerated Approval pathway ~ ~ BLA submission planned for first quarter of 2026 ~ ~ Conference call today at 8:30 a.m. ET ~ LEXINGTON, Mass. and AMSTERDAM, June 02, 2025 (GLOBE NEWSWIRE) -- uniQure N.V. (NASDAQ:QURE), a leading gene therapy company advancing transformative therapies for patients with severe medical needs, today provided a regulatory update on AMT-130, its investigational gene therapy for the treatment of Huntington's disease. Following recent Type B meetings and further guidance from the U.S. Food and Drug Administration (FDA), the Company has reached alignment with the FDA on several key components of the statistical analysis
~ No serious adverse events and 92% reduction in seizure frequency observed in the first trial participant through first five months of follow up ~ ~ Data to be presented today at Epilepsy Therapies & Diagnostics Development Symposium (ETDD) ~ LEXINGTON, Mass. and AMSTERDAM, May 29, 2025 (GLOBE NEWSWIRE) -- uniQure N.V. (NASDAQ:QURE), a leading gene therapy company advancing transformative therapies for patients with severe medical needs, today announced the presentation of a clinical case study of the first participant dosed in the first cohort of its ongoing Phase I/IIa trial of an investigational gene therapy candidate, AMT-260, in patients with refractory MTLE. The data are being