QURE UNIQURE NV

uniQure Announces Multiple Presentations at Upcoming American Society of Gene and Cell Therapy (ASGCT) Annual Meeting

uniQure Announces Multiple Presentations at Upcoming American Society of Gene and Cell Therapy (ASGCT) Annual Meeting

LEXINGTON, Mass. and AMSTERDAM, May 02, 2022 (GLOBE NEWSWIRE) -- (NASDAQ: QURE), a leading gene therapy company advancing transformative therapies for patients with severe medical needs, today announced that six data presentations, including one oral presentation, will be delivered at the American Society of Gene and Cell Therapy (ASGCT) Hybrid Congress 2022 Annual Meeting being held May 16-19 in Washington, D.C.

"Our presentations at ASGCT showcase the exceptional work of our uniQure scientists and the breadth of our research pipeline as we advance our investigational AAV gene therapy programs,” stated Ricardo Dolmetsch, Ph.D. president of research and development at uniQure. “We are particularly proud of our studies demonstrating the potential of the linQURE® cargo platform, delivering multiple miRNAs in a single AAV and its application to selectively silence mutant C9orf72 in an ALS preclinical model.”

Specific details on uniQure’s presentations taking place at ASGCT include:

  • Title: Alpha-synuclein lowering and rescue of motor phenotype by miRNA-based AAV gene therapy in in vivo Parkinson’s disease models (Abstract #19)

    Presenter: Astrid Valles-Sanchez, Ph.D. director of CNS disease biology, uniQure

    Oral Session Title: Oligonucleotide Therapeutics

    Date and Time: Monday, May 16, 11:15 – 11:30 a.m. EDT
  • Title: Construction and optimization of novel adeno-associated virus (AAV) rep gene expression control system for stable rAAV-packaging insect cell line (Abstract #407)

    Poster Session Title: Vector Product Engineering, Development or Manufacturing I

    Session Date and Time: Monday, May 16, 5:30 – 6:30 p.m. EDT
  • Title: Functional transfer of engineered microRNAs through extracellular vesicles: An in vitro proof-of-mechanism study in Huntington’s disease models (Abstract #590)

    Poster Session Title: Oligonucleotide Therapeutics II

    Session Date and Time: Tuesday, May 17, 5:30 – 6:30 p.m. EDT
  • Title: Selective silencing of mutant C9orf72 transcripts (Abstract #552)

    Poster Session Title: Gene Targeting and Gene Correction II

    Date and Time: Tuesday, May 17, 5:30 – 6:30 p.m. EDT
  • Title: AAV5-GLA gene therapy results in sustained long term GLA transgene expression and cross correction of target organs in Fabry disease mouse model (Abstract #1009)

    Poster Session Title: Metabolic, Storage, Endocrine, Liver and Gastrointestinal Diseases II

    Session Date and Time: Wednesday, May 18, 5:30 p.m. EDT
  • Title: AAV-mediated APOE gene silencing for Alzheimer’s disease (Abstract #918)

    Poster Session Title: AAV Vectors - Preclinical and Proof-of-concept Studies III

    Date and Time: Wednesday, May 18, 5:30 p.m. EDT

About uniQure

uniQure is delivering on the promise of gene therapy – single treatments with potentially curative results. We are leveraging our modular and validated technology platform to rapidly advance a of proprietary gene therapies to treat patients with hemophilia B, Huntington's disease, refractory temporal lobe epilepsy, Fabry disease, and other diseases. 

uniQure Contacts:

FOR INVESTORS:  FOR MEDIA:
   
Maria E. Cantor

Direct: 339-970-7536

Mobile: 617-680-9452

Chiara Russo

Direct: 617-306-9137

Mobile: 617-306-9137



Tom Malone

Direct: 339-970-7558

Mobile:339-223-8541





EN
02/05/2022

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on UNIQURE NV

 PRESS RELEASE

uniQure Announces 2025 Financial Results and Provides Recent Company U...

uniQure Announces 2025 Financial Results and Provides Recent Company Updates ~ Held Type A meeting with FDA to discuss AMT-130 for Huntington’s disease; Company evaluating Phase III development considerations and plans to request follow-up Type B meeting in the second quarter of 2026 ~ ~ Completed enrollment of the first cohort in the Phase I/IIa study of AMT-260 in refractory mesial temporal lobe epilepsy, with additional clinical data expected in the first half of 2026 ~ ~ Presented updated Phase I/II data from AMT-191 in Fabry disease showing durable, dose-dependent increases in α-Gal ...

 PRESS RELEASE

uniQure Provides Regulatory Update on AMT-130 for Huntington’s Disease

uniQure Provides Regulatory Update on AMT-130 for Huntington’s Disease LEXINGTON, Mass. and AMSTERDAM, March 02, 2026 (GLOBE NEWSWIRE) -- N.V. (NASDAQ: QURE), a leading gene therapy company advancing transformative therapies for patients with severe medical needs, today announced that the company received final meeting minutes from the U.S. Food and Drug Administration (FDA) regarding a Type A meeting held on January 30, 2026 to discuss AMT-130, an investigational gene therapy for Huntington’s disease (HD).   The FDA stated that it cannot agree that data from the Phase I/II studies, com...

 PRESS RELEASE

uniQure to Announce 2025 Financial Results

uniQure to Announce 2025 Financial Results ~ uniQure to host earnings call on Monday, March 2, 2026 at 8:00 a.m. ET ~ LEXINGTON, Mass. and AMSTERDAM, Feb. 23, 2026 (GLOBE NEWSWIRE) -- N.V. (NASDAQ: QURE), a leading gene therapy company advancing transformative therapies for patients with severe medical needs will report fourth quarter and full year of 2025 financial results before market open on Monday, March 2, 2026. Management will then host a conference call at 8:00 a.m. ET. The event will be webcast under the Events & Presentations section of uniQure’s website at , and following t...

 PRESS RELEASE

uniQure Announces Updated Preliminary AMT-191 Phase I/IIa Data Showing...

uniQure Announces Updated Preliminary AMT-191 Phase I/IIa Data Showing Sustained Increases in α-Gal A Enzyme Activity in Patients with Fabry Disease ~ Supraphysiological expression of α-Gal A activity maintained for over a year in longest treated patient as of data cutoff date ~ ~ Stable Lyso-Gb3 levels maintained post-dosing, regardless of enzyme replacement therapy status across all cohorts ~ ~ Six of 11 patients have discontinued enzyme replacement therapy as of data cutoff date ~ LEXINGTON, Mass. and AMSTERDAM, Feb. 06, 2026 (GLOBE NEWSWIRE) -- N.V. (NASDAQ: QURE), a leading gene ...

 PRESS RELEASE

uniQure Announces Type A Meeting Scheduled with FDA

uniQure Announces Type A Meeting Scheduled with FDA LEXINGTON, Mass. and AMSTERDAM, Jan. 09, 2026 (GLOBE NEWSWIRE) -- N.V. (NASDAQ: QURE), a leading gene therapy company advancing transformative therapies for patients with severe medical needs, today announced a Type A meeting with the U.S. Food and Drug Administration (FDA) has been scheduled to discuss the Biologics License Application (BLA) data package to support accelerated approval of AMT-130, the Company’s investigational gene therapy for the treatment of Huntington’s disease. “We look forward to a constructive discussion with th...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch