LoQus23 Therapeutics announces £35 million financing to advance a new drug aimed at inhibiting somatic expansion in Huntington’s Disease

Cambridge, UK, 2 October 2024 – LoQus23 Therapeutics Ltd (“LoQus23”), a private biotechnology company investigating small molecule drugs that could stop DNA instability and slow neurodegeneration in Huntington’s Disease, myotonic dystrophy type 1 and similar triplet repeat expansion diseases, today announces Lire la suite...

La Pridopidine de Prilenia pour la maladie de Huntington acceptée pour l'examen de l'autorisation de mise sur le marché européen

Prilenia, a clinical stage biotechnology company focused on the urgent mission to develop novel therapeutics to slow the progression of neurodegenerative diseases and neurodevelopmental disorders, has filed a European Marketing Authorization Application (MAA) with the European Medicines Agency (EMA) for Lire la suite...

L'IROS, Prilenia et l'Association internationale de la maladie de Huntington collaborent à la réalisation du tout premier essai clinique sur la maladie de Huntington (MH) dans la région MENA

Abu Dhabi, UAE; June 19, 2024: IROS, an Abu Dhabi-based contract research organization (part of the M42 group), has partnered with Prilenia Therapeutics, a clinical-stage biotech company, and the International Huntington’s Disease Association (IHA) to plan the first-ever clinical trial Lire la suite...

uniQure annonce des données intermédiaires positives démontrant un ralentissement de la progression de la maladie dans les essais de phase I/II de l'AMT-130 pour la MH

“We are very pleased with these new data demonstrating a statistically significant, dose-dependent slowing of the progression of Huntington’s disease and lowering of NfL in the CSF at 24 months,” stated Walid Abi-Saab, M.D., chief medical officer of uniQure. “We believe Lire la suite...

Wave Life Sciences annonce des résultats positifs de l'essai de phase 1b/2a SELECT-HD avec la première démonstration clinique de l'abaissement sélectif de l'allèle de la huntingtine mutante dans la maladie de Huntington.

Today, Wave Life Sciences announced positive results from SELECT-HD, our Phase 1b/2a placebo-controlled trial evaluating the investigational therapy WVE-003. These results demonstrate that WVE-003 selectively lowers toxic, mutant huntingtin (mHTT) protein and preserves healthy, wild-type huntingtin (wtHTT) protein for individuals Lire la suite...

fr_FRFrench
Aller au contenu principal