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uniQure Announces Second Quarter 2025 Financial Results and Highlights of Recent Company Progress
July 29, 2025
From
uniQure Inc.
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uniQure to Announce Second Quarter 2025 Financial Results
July 22, 2025
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uniQure Inc.
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uniQure Announces Appointment of Kylie O’Keefe as Chief Customer and Strategy Officer
June 11, 2025
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uniQure Provides Regulatory Update on AMT-130 for Huntington’s Disease
June 02, 2025
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uniQure Presents Clinical Case Study of First Patient Dosed with AMT-260 in Refractory Mesial Temporal Lobe Epilepsy (MTLE)
May 29, 2025
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uniQure Announces First Quarter 2025 Financial Results and Highlights of Recent Company Progress
May 09, 2025
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uniQure to Announce First Quarter 2025 Financial Results
May 05, 2025
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uniQure Announces FDA Breakthrough Therapy Designation Granted to AMT-130 for the Treatment of Huntington’s Disease
April 17, 2025
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uniQure Announces 2024 Financial Results and Highlights Recent Company Progress
February 27, 2025
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uniQure Announces Completion of Enrollment in the First Cohort and Favorable Recommendation from the Independent Data Monitoring Committee for its Phase I/IIa Clinical Trial of AMT-191 for the Treatment of Fabry Disease
February 03, 2025
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uniQure Announces Favorable Recommendation from Independent Data Monitoring Committee for its Phase I/II EPISOD1 Clinical Trial of AMT-162 for the Treatment of SOD1-ALS
January 30, 2025
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uniQure Announces Pricing of its Public Offering
January 08, 2025
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uniQure Announces Proposed Public Offering
January 07, 2025
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uniQure Announces Alignment with FDA on Key Elements of Accelerated Approval Pathway for AMT-130 in Huntington’s Disease
December 10, 2024
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uniQure Announces Dosing of First Patient in GenTLE Phase I/IIa Clinical Trial of AMT-260 for the Treatment of Refractory Mesial Temporal Lobe Epilepsy
November 21, 2024
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uniQure Announces Third Quarter 2024 Financial Results and Highlights Recent Company Progress
November 05, 2024
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uniQure Announces Dosing of First Patient in Phase I/II Clinical Trial of AMT-162 for the Treatment SOD1-ALS
October 15, 2024
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uniQure Announces Orphan Drug Designation Granted to AMT-191 for the Treatment of Fabry Disease
September 23, 2024
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uniQure Announces Dosing of First Patient in Phase I/IIa Clinical Trial of AMT-191 for the Treatment of Fabry Disease
August 15, 2024
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uniQure Announces Second Quarter 2024 Financial Results and Provides Company Update
August 01, 2024
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uniQure Announces Closing of Sale of Manufacturing Facility to Genezen
July 23, 2024
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uniQure Announces Positive Interim Data Update Demonstrating Slowing of Disease Progression in Phase I/II Trials of AMT-130 for Huntington’s Disease
July 09, 2024
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uniQure Announces Sale of Commercial Manufacturing Facility to Genezen
July 01, 2024
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uniQure Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for Investigational Gene Therapy AMT-130 in Huntington’s Disease
June 03, 2024
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uniQure Announces First Quarter 2024 Financial Results and Highlights Recent Company Progress
May 07, 2024
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uniQure Announces 2023 Financial Results and Highlights Recent Company Progress
February 28, 2024
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uniQure Announces Update on Phase I/II Clinical Trials of AMT-130 Gene Therapy for the Treatment of Huntington’s Disease
December 19, 2023
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uniQure Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
December 08, 2023
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uniQure Announces FDA Clearance of Investigational New Drug Application for AMT-191 Gene Therapy for Fabry Disease
November 29, 2023
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uniQure Announces Third Quarter 2023 Financial Results and Highlights Recent Company Progress
November 07, 2023
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