Международная ассоциация Хантингтона теперь является членом Международной организации по редким заболеваниям!

It is official! The International Huntington Association is now a part of RDI, Rare Diseases International. This is a huge step for IHA, as it means we are not only […]
Компания uniQure сообщает о результатах клинических испытаний I/II фазы генной терапии AMT-130 для лечения болезни Хантингтона

~ Patients treated with AMT-130 continue to show evidence of preserved neurological function with potential dose-dependent clinical benefits relative to an inclusion criteria-matched natural history of the disease ~ ~ Mean […]
Расширение возможностей сообществ: Обзор последних инициатив Бразильской ассоциации хантинга (ABH)

The Brazilian Huntington Association (ABH – Associação Brasil Huntington) is incredibly active and has been conducting numerous initiatives for the community. This level of commitment is vital because it not […]
Эшли Кларк, HD Advocate, делится своим опытом работы в штаб-квартире uniQure

As well as being an ambassador for the Huntington’s Disease Youth Organisation (HDYO) Ashley Clarke is an advocate for the HD-Community Advisory Board (HD-CAB), a group that represents the patient […]
Rise Against Huntington's: как два молодых школьника собрали $2000 на лечение болезни Хантингтона

Jasmine and Sai are high school students from the US. They’re two young people who are determined to make a difference and inspire others to follow suit. A fundraising initiative […]
Национальный день борьбы с болезнью Хантингтона официально учрежден в Бразилии

After being approved by the Chamber of Deputies last year, the Bill 5060/13 was finally published in the Official Diary of the Union last month, 21st of June, establishing the […]
О приключениях Дмитрия Поффе (Explore for Huntington) рассказывается в новом документальном фильме

The HD Community already knows Dimitri Poffé’s adventures too well, and now, the world will too. The French traveler who is doing a bicycle trip through all South America to […]
MENA Organization for Rare Diseases Annual Meeting & Exhibition 2024

MENA Organization for Rare Diseases announces the third annual meeting, MENA Organization for Rare Diseases Annual Meeting & Exhibition 2024 that will be held in Movenpick Grand Al Bustan Dubai […]
PTC Therapeutics делится положительными промежуточными данными клинического испытания PIVOT-HD на пациентах с болезнью Хантингтона

June 21, 2023 PDF Version – Dose-dependent lowering of blood Huntingtin (HTT) protein levels at 12 weeks –– Favorable tolerability profile with no treatment-related serious adverse events or NfL spikes – – Conference […]
Компания uniQure объявляет о проведении в США I/II фазы клинических испытаний генной терапии AMT-130 для лечения болезни Хантингтона

~ AMT-130 continues to be generally well-tolerated across both dose cohorts ~ ~ Patients treated with AMT-130 show preserved function compared to baseline and clinical benefits relative to natural history […]