{"id":6211,"date":"2026-02-17T15:37:49","date_gmt":"2026-02-17T12:37:49","guid":{"rendered":"https:\/\/dmdwarrior.com\/?p=6211"},"modified":"2026-02-17T15:39:39","modified_gmt":"2026-02-17T12:39:39","slug":"data-monitoring-committee-recommended-initiating-an-increased-dose-for-group-2-in-entrada-therapeutics-exon-44-skipping-study","status":"publish","type":"post","link":"https:\/\/dmdwarrior.com\/fr\/data-monitoring-committee-recommended-initiating-an-increased-dose-for-group-2-in-entrada-therapeutics-exon-44-skipping-study\/","title":{"rendered":"Le comit\u00e9 de surveillance des donn\u00e9es a recommand\u00e9 l&#039;instauration d&#039;une dose plus \u00e9lev\u00e9e pour le groupe 2 de l&#039;\u00e9tude de saut d&#039;exon 44 du g\u00e8ne Entrada."},"content":{"rendered":"<p class=\"wp-block-paragraph\"><strong>Entrada Therapeutics a annonc\u00e9 qu&#039;un comit\u00e9 ind\u00e9pendant de surveillance des donn\u00e9es (DMC), conform\u00e9ment au protocole de l&#039;\u00e9tude, a examin\u00e9 toutes les donn\u00e9es de s\u00e9curit\u00e9 et de PK disponibles des huit patients qui ont termin\u00e9 le dosage dans la cohorte 1 de la partie \u00e0 double aveugle, contr\u00f4l\u00e9e par placebo et \u00e0 doses multiples croissantes (MAD) de ELEVATE-44-201.<\/strong><\/p>\n\n\n\n<h2 class=\"wp-block-heading\">La recommandation d&#039;une augmentation de la dose est un indicateur de r\u00e9sultats positifs.<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">\u201c Nous sommes heureux qu\u2019apr\u00e8s avoir examin\u00e9 les donn\u00e9es de la cohorte 1 de notre \u00e9tude ELEVATE-44-201, le comit\u00e9 ind\u00e9pendant de surveillance des donn\u00e9es soutienne le lancement de l\u2019administration du dosage \u00e0 la cohorte 2 \u00e0 une dose accrue de 12 mg\/kg \u201d, a d\u00e9clar\u00e9 Natarajan Sethuraman, PhD, pr\u00e9sident de la recherche et du d\u00e9veloppement chez Entrada Therapeutics. <strong>\u201c \u00c9tant donn\u00e9 que tous les programmes neuromusculaires de Entrada exploitent le m\u00eame v\u00e9hicule d&#039;\u00e9chappement endosomal, nous sommes convaincus que la progression de cette \u00e9tude r\u00e9duit consid\u00e9rablement les risques de nos programmes cliniques et marque un tournant clinique important pour notre entreprise. \u00bb.<\/strong> L&#039;\u00e9tablissement de l&#039;innocuit\u00e9 du ENTR-601-44 \u00e0 la dose de 6 mg\/kg constitue une \u00e9tape importante pour le programme. Nous pr\u00e9voyons que les donn\u00e9es de la cohorte 1 \u00e0 6 mg\/kg montreront une production de dystrophine \u00e0 deux chiffres lors de leur publication au deuxi\u00e8me trimestre. En augmentant progressivement la dose jusqu&#039;\u00e0 12 mg\/kg, nous pensons atteindre une restauration de la dystrophine optimale, comme le confirmeront les donn\u00e9es de la cohorte 2 plus tard cette ann\u00e9e.\u201d<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">ELEVATE-44-201 est une \u00e9tude mondiale en deux parties, randomis\u00e9e, en double aveugle, contr\u00f4l\u00e9e par placebo, de phase 1\/2 \u00e9valuant la s\u00e9curit\u00e9, la tol\u00e9rance et l&#039;efficacit\u00e9 de ENTR-601-44 chez les patients ambulatoires atteints de DMD qui sont susceptibles de subir un saut de l&#039;exon 44. <strong>La soci\u00e9t\u00e9 a termin\u00e9 l&#039;administration du traitement \u00e0 dose maximale administr\u00e9e (MAD) pour la cohorte 1, et les participants sont pass\u00e9s \u00e0 la phase 2, en ouvert, comportant 6 doses. La soci\u00e9t\u00e9 pr\u00e9voit de publier les donn\u00e9es de la cohorte 1 (6 mg\/kg) au deuxi\u00e8me trimestre 2026, celles de la cohorte 2 (12 mg\/kg) d&#039;ici la fin de l&#039;ann\u00e9e, et celles de la cohorte 3 (jusqu&#039;\u00e0 18 mg\/kg) ult\u00e9rieurement. <\/strong>La soci\u00e9t\u00e9 pr\u00e9voit \u00e9galement d&#039;ouvrir une cohorte d&#039;expansion plus tard dans l&#039;ann\u00e9e afin d&#039;augmenter le nombre de participants trait\u00e9s dans l&#039;\u00e9tude ELEVATE-44-201, car cette \u00e9tude a \u00e9t\u00e9 con\u00e7ue pour soutenir une approbation acc\u00e9l\u00e9r\u00e9e aux \u00c9tats-Unis. En d\u00e9cembre 2025, la Food and Drug Administration am\u00e9ricaine (FDA) a accord\u00e9 la d\u00e9signation de maladie p\u00e9diatrique rare \u00e0 ENTR-601-44.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Apprendre encore plus<\/strong>:\u00a0<a href=\"https:\/\/dmdwarrior.com\/fr\/upcoming-exon-44-skipping-therapies-for-dmd\/\">Th\u00e9rapies par saut d&#039;exon 44 \u00e0 venir pour le traitement de la maladie de Duchenne<\/a><\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Mutations et d\u00e9l\u00e9tions sensibles aux th\u00e9rapies de saut d&#039;exon 44 pour la dystrophie musculaire de Duchenne<\/h2>\n\n\n\n<figure class=\"wp-block-image size-large\"><img decoding=\"async\" width=\"968\" height=\"1024\" src=\"https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-968x1024.jpg\" alt=\"Mutations et d\u00e9l\u00e9tions sensibles aux th\u00e9rapies de saut d&#039;exon 44 pour la dystrophie musculaire de Duchenne\" class=\"wp-image-5275\" title=\"\" srcset=\"https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-968x1024.jpg 968w, https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-284x300.jpg 284w, https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-768x813.jpg 768w, https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-1452x1536.jpg 1452w, https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-11x12.jpg 11w, https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-397x420.jpg 397w, https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-150x159.jpg 150w, https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-300x317.jpg 300w, https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-696x737.jpg 696w, https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping-1068x1130.jpg 1068w, https:\/\/dmdwarrior.com\/wp-content\/uploads\/2025\/11\/Deletions-Amenable-to-Exon-44-Skipping.jpg 1890w\" sizes=\"(max-width: 968px) 100vw, 968px\" \/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Suivre cette page<\/strong>\u00a0>>>\u00a0<a href=\"https:\/\/dmdwarrior.com\/fr\/dmd-therapies\/\" target=\"_blank\" rel=\"noreferrer noopener\">Tous les essais cliniques pour la dystrophie musculaire de Duchenne<\/a><\/p>","protected":false},"excerpt":{"rendered":"<p>Entrada Therapeutics announced that an independent Data Monitoring Committee (DMC), per study protocol, has reviewed all available safety and PK data from the eight patients who completed dosing in Cohort 1 of the double-blinded, placebo-controlled, multiple ascending dose (MAD) portion of ELEVATE-44-201. Dose increase recommendation is an indicator of positive results \u201cWe are pleased that [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":6213,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[281],"tags":[233,234,141,127,246],"class_list":["post-6211","post","type-post","status-publish","format-standard","has-post-thumbnail","category-press-releases","tag-entrada","tag-entrada-therapeutics","tag-exon-44","tag-exon-44-skipping","tag-exon-44-skipping-therapies"],"subtitle":"Le Comit\u00e9 ind\u00e9pendant de surveillance des donn\u00e9es a recommand\u00e9 le lancement de la cohorte 2 \u00e0 12 mg\/kg, une augmentation de dose par rapport \u00e0 6 mg\/kg dans la cohorte 1. ELEVATE-44-201 est une \u00e9tude clinique MAD de phase 1\/2 de ENTR-601-44 pour le traitement potentiel de la dystrophie musculaire de Duchenne (DMD) chez les patients pr\u00e9sentant une mutation confirm\u00e9e du g\u00e8ne DMD susceptible de b\u00e9n\u00e9ficier d'un saut de l'exon 44.","_links":{"self":[{"href":"https:\/\/dmdwarrior.com\/fr\/wp-json\/wp\/v2\/posts\/6211","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/dmdwarrior.com\/fr\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/dmdwarrior.com\/fr\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/dmdwarrior.com\/fr\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/dmdwarrior.com\/fr\/wp-json\/wp\/v2\/comments?post=6211"}],"version-history":[{"count":0,"href":"https:\/\/dmdwarrior.com\/fr\/wp-json\/wp\/v2\/posts\/6211\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/dmdwarrior.com\/fr\/wp-json\/wp\/v2\/media\/6213"}],"wp:attachment":[{"href":"https:\/\/dmdwarrior.com\/fr\/wp-json\/wp\/v2\/media?parent=6211"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/dmdwarrior.com\/fr\/wp-json\/wp\/v2\/categories?post=6211"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/dmdwarrior.com\/fr\/wp-json\/wp\/v2\/tags?post=6211"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}