Sage Therapeutics fas 2-studie förstärker den kognitiva påverkan av Huntingtons sjukdom

Earlier this week Sage Therapeutics announced the results of their SURVEYOR study which quantified the cognitive impact of Huntington’s Disease. Using the HD-Cognitive Assessment Battery (HD-CAB) they measured the difference […]
FDA beviljar uniQure Regenerative Medicine Advance Therapy (RMAT) Designation

Idag är vi mycket glada i Huntington-communityn. Tillkännagivandet från Uniqure att företaget har fått Regenerative Medicine Advanced Therapy (RMAT) "Designation for Investigational Gene Therapy AMT-130 [...]
SOM Biotech slutför rekryteringsprocessen i fas IIb-studien av behandling av chorea vid Huntingtons sjukdom

SOM Biotech, a clinical-stage drug discovery and development company based on a unique proprietary Artificial Intelligence platform (SOMAIPRO®), is pleased to announce that the recruitment of the Phase IIb clinical […]
Prilenia planerar att lämna in ansökan om marknadsgodkännande i EU för pridopidin vid Huntingtons sjukdom

Prilenia announced today that they plan to submit a Marketing Authorization Application in the EU for the use of Pridopidine in the treatment of Huntington’s Disease. According to Dr. Michael […]
Genombrott innebär nytt hopp för HD-patienter

Scientists from the Weizmann Institute in Israel have published the results of an animal study which holds tremendous promise for the treatment of Huntington’s Disease. They have discovered that two […]
uniQure meddelar uppdatering om kliniska fas I/II-studier av AMT-130 genterapi för behandling av Huntingtons sjukdom

~ 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 […]
PTC Therapeutics delar med sig av positiva interimsdata från den kliniska studien PIVOT-HD i patienter med Huntingtons sjukdom

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 […]
uniQure meddelar uppdatering om klinisk fas I/II-studie i USA med genterapin AMT-130 för behandling av Huntingtons sjukdom

~ 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 […]
PRILENIA TILLKÄNNAGER RESULTAT FRÅN PROOF-HD-STUDIEN: LOVANDE, MEN BLANDADE RESULTAT!

Today, April 25th, Prilenia announced results from the PROOF-HD clinical trial for Huntington’s Disease. Some of the participants showed significant benefits from the Pridopidine drug, while others did not benefit at all. This […]
Prilenia uppnår sista patientens sista besök i den kliniska fas 3-studien PROOF-HD för Huntingtons sjukdom

PROOF-HD är den enda studien i sen fas av Huntingtons sjukdom som riktar in sig på klinisk progression; topline-resultat förväntas i början av Q2 2023 NAARDEN, Nederländerna och WALTHAM, 28 mars 2023 - Prilenia Therapeutics B.V., ett [...].