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Satellos Announces Formation of Clinical Advisory Board to Support Advancing SAT-3247 in Clinical Trial Development for Duchenne Muscular Dystrophy

Satellos expects to begin first-in-human clinical trials mid-year for SAT-3247, an oral small molecule drug candidate in development as a novel regenerative medicine approach to treating DMD .

Perry shiehFrancesco muntoniFrank gleesonRonald cohnHanns lochmRichard finkelNicholas johnsonMyology researchSatellos bioscience incJude children research hospitalInstitute of child healthDavid geffen school of medicineDubowitz neuromuscular centreGeorge bliley researchChildren hospital of eastern ontario research instituteSatellos bioscience

Satellos Bioscience Inc Announces Formation of Clinical Advisory Board

Satellos Bioscience Inc. announced the formation of a Clinical Advisory Board comprised of distinguished clinical research leaders and experts in drug development in genetic muscle disorders,.

Richard finkelNicholas johnsonHanns lochmRonald cohnFrancesco muntoniPerry shiehGeorge bliley researchInstitute of child healthSatellos bioscience incMyology researchDubowitz neuromuscular centreHospital of eastern ontario research instituteDavid geffen school of medicineJude children research hospitalSatellos bioscienceClinical advisory board

Genethon: First Clinical Trial Results of Gene Therapy (GNT0004) for Duchenne Muscular Dystrophy Presented at International Myology 2024 Congress

Genethon: First Clinical Trial Results of Gene Therapy (GNT0004) for Duchenne Muscular Dystrophy Presented at International Myology 2024 Congress
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France generalUnited kingdomDennis riedlFrancesco muntoniData monitoring committeeInstitute of myology parisDickson university of londonEuropean medicines agencyProfessor francesco muntoniDuchenne muscular dystrophyDuchenne muscularNorth star ambulatory assessmentWalk testRoyal hollowayAktien sie

Beyond Traditional Placebo Controls in Rare Disease Clinical Trials: New cTAP Evidence Supports Patient-Centric Alternatives

/PRNewswire/ The Collaborative Trajectory Analysis Project (cTAP), a global coalition in rare disease, has announced evidence to support patient-centric.

United kingdomCity ofFrancesco muntoniJames signorovitchPrincipal at analysis groupInstitute of child healthCollaborative trajectory analysis projectDuchenne muscular dystrophyProfessor francesco muntoniPaediatric neurologyOrmond street instituteChild healthGreat ormond street hospitalManaging principalExecutive directorCollaborative trajectory analysis project ctap

Repeated intravenous cardiosphere-derived cell therapy in late-stage Duchenne muscular dystrophy (HOPE-2): a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial

Repeated intravenous cardiosphere-derived cell therapy in late-stage Duchenne muscular dystrophy (HOPE-2): a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial
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Beverly hillsUnited statesUnited kingdomCity ofVeena ramanna capricorEpirium bioCapricor tharapeuticsJ baek sacramentoSam dicksonMallinckrodt pharmaceuticalsRehabilitation researchAtom internationalMallinkrodt pharmaceuticalsTherapy solutionsNational institute on disabilityLogan kowallis pentara corporation