{"id":3036,"date":"2024-06-14T22:20:28","date_gmt":"2024-06-14T14:20:28","guid":{"rendered":"https:\/\/flcube.com\/?p=3036"},"modified":"2024-10-18T00:30:49","modified_gmt":"2024-10-17T16:30:49","slug":"pfizers-gene-therapy-for-duchenne-muscular-dystrophy-misses-late-stage-trial-endpoints","status":"publish","type":"post","link":"https:\/\/flcube.com\/?p=3036","title":{"rendered":"Pfizer&#8217;s Gene Therapy for Duchenne Muscular Dystrophy Misses Late-Stage Trial Endpoints"},"content":{"rendered":"\n<p>Pfizer Inc. (<a href=\"https:\/\/www.google.com\/finance\/quote\/PFE:NYSE\">NYSE: PFE<\/a>) has announced that a late-stage clinical trial for its investigational gene therapy, fordadistrogene movaparvovec, in children aged 4 to 7 with Duchenne muscular dystrophy (DMD) failed to meet its primary endpoint of improving motor function. Additionally, secondary endpoints related to motor function showed no significant improvement compared to the placebo group.<\/p>\n\n\n\n<p>This marks the second major setback for the program, as it had already been placed on a dosing pause due to a fatal serious adverse event that occurred in a Phase II study involving children aged 2 to 3 years.<\/p>\n\n\n\n<p>Despite these challenges, Pfizer has indicated that the safety profile of the gene therapy remained manageable throughout the trial.- <a href=\"https:\/\/flcube.com\">Flcube.com<\/a><\/p>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Pfizer Inc. (NYSE: PFE) has announced that a late-stage clinical trial for its investigational gene&#8230;<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"googlesitekit_rrm_CAownpewDA:productID":"","_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[7,11],"tags":[66,863,68,309],"class_list":["post-3036","post","type-post","status-publish","format-standard","hentry","category-company","category-drug","tag-gene-therapy","tag-nyse-pfe","tag-pediatric-drugs","tag-pfizer"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v23.6 (Yoast SEO v27.5) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>Pfizer&#039;s Gene Therapy for Duchenne Muscular Dystrophy Misses Late-Stage Trial Endpoints - Insight, China&#039;s Pharmaceutical Industry<\/title>\n<meta name=\"description\" content=\"Pfizer Inc. (NYSE: PFE) has announced that a late-stage clinical trial for its investigational gene therapy, fordadistrogene movaparvovec, in children aged 4 to 7 with Duchenne muscular dystrophy (DMD) failed to meet its primary endpoint of improving motor function. Additionally, secondary endpoints related to motor function showed no significant improvement compared to the placebo group.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/flcube.com\/?p=3036\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Pfizer&#039;s Gene Therapy for Duchenne Muscular Dystrophy Misses Late-Stage Trial Endpoints\" \/>\n<meta property=\"og:description\" content=\"Navigate the complexities of China\u2019s pharmaceutical industry with precision and clarity. 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