PRESS RELEASE published on 04/23/2024 at 07:30, 2 years 1 month ago Theranexus, Diverchim and Inserm awarded EUR 4.7 million in funding under the "Innovations in biotherapies and biomanufacturing" call for proposals from France 2030 to develop a novel antisense oligonucleotide Theranexus, Diverchim, and Inserm's ARNA laboratory receive €4.7 million funding from French Government to develop autophagy activation therapy for rare neurological diseases under the PickASO project in collaboration with France 2030 Theranexus Diverchim Autophagy Activation Therapy Inserm PickASO Project
BRIEF published on 04/18/2024 at 18:05, 2 years 2 months ago Theranexus et BBDF annoncent des résultats positifs pour l'étude de phase 1/2 de Batten-1 Étude Clinique Maladies Rares Theranexus Maladie De Batten CLN3 Batten-1
BRIEF published on 04/18/2024 at 18:05, 2 years 2 months ago Theranexus and BBDF Announce Positive Results for Batten-1 Phase 1/2 Study Clinical Study Rare Diseases Theranexus Batten-1 Batten Disease CLN3
PRESS RELEASE published on 04/18/2024 at 18:00, 2 years 2 months ago Theranexus et BBDF annoncent les données finales et positives de sécurité et d'efficacité de Batten-1 dans l'étude de phase 1/2 Theranexus et la Fondation BBDF annoncent des données positives sur la stabilisation des symptômes moteurs chez les patients jeunes adultes atteints de la maladie de Batten CLN3 après 18 mois de traitement Theranexus Fondation BBDF Maladie De Batten Stabilisation Symptômes Moteurs Traitement Batten-1
PRESS RELEASE published on 04/18/2024 at 18:00, 2 years 2 months ago Theranexus and BBDF announce final and positive safety and efficacy data in the Phase I/II trial testing Batten-1 Theranexus and BBDF announce positive final results after 18-month Phase I/II trial of Batten-1 in juvenile Batten disease (CLN3) patients, showing stabilization of motor symptoms progression in young adults Theranexus Batten-1 BBDF Juvenile Batten Disease Phase I/II Trial
PRESS RELEASE published on 05/10/2023 at 16:59, 3 years 1 month ago Theranexus et BBDF obtiennent l'accord de la FDA sur les critères d'efficacité de l'étude de phase 3 de Batten-1 dans la maladie de Batten CLN3
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