QURE UNIQURE NV

uniQure to Participate in Upcoming Industry Conferences in November

uniQure to Participate in Upcoming Industry Conferences in November

LEXINGTON, Mass. and AMSTERDAM, Nov. 01, 2021 (GLOBE NEWSWIRE) -- (NASDAQ: QURE), a leading gene therapy company advancing transformative therapies for patients with severe medical needs, today announced its participation in the following upcoming investor and scientific conferences:

  • The 28th Annual Meeting of the Huntington Study Group (Virtual), November 4 - 6, 2021



    • David Cooper, M.D., vice president of clinical research CNS, will present an overview of the ongoing clinical trials of AMT-130 in Huntington’s Disease, HD-GeneTRX-1 and -2, and participate in a Q&A session on Friday, November 5th at 3:15 p.m. ET.



    • An encore poster presentation entitled, “Demographics and healthcare resource utilization (HRU) in US patients with Huntington’s Disease: data from the Huntington’s Disease Burden of Illness (HDBOI) study” will also be available to view at the Poster Pavilion to registered participants.



  • Virtual Neuroscience 2021 – 50th Annual Meeting, November 8 - 11, 2021



    • Corlieve academic collaborator, Valeria Crepel, Ph.D., will present an encore presentation “CL002, An AAV9 vector expressing engineered miRNA targeting knockdown of GluK2-containing kainite receptors as a novel gene therapy approach for treating intractable temporal lobe epilepsy” on Thursday, November 11th at 10:00 a.m. ET, Session P152: Antiepileptic Therapies IV.



  • Stifel 2021 Virtual Healthcare Conference, November 15 - 17, 2021



    • Members of uniQure’s management team, including , chief executive officer, will participate in virtual one-on-one investor meetings on Wednesday, November 17th.



    • A fireside chat with Mr. Kapusta will take place the same day from 10:40 to 11:10 a.m. ET. The live webcast of the fireside chat can be accessed through the link displayed in the section of the uniQure website.

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 severe genetic diseases of the central nervous system (CNS) and liver, including clinical programs in hemophilia B and Huntington's disease and preclinical candidates in Fabry disease, spinocerebellar ataxia Type 3, temporal lobe epilepsy, Alzheimer’s, Parkinson’s, and ALS.

uniQure Contacts:

FOR INVESTORS: FOR MEDIA:
   
Maria E. CantorChiara RussoTom Malone
Direct: 339-970-7536Direct: 617-306-9137Direct: 339-970-7558


EN
01/11/2021

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