Solid Biosciences Inc. (SLDB)
Solid Biosciences Inc. is an American biotechnology firm dedicated to creating therapeutic solutions for Duchenne Muscular Dystrophy (DMD). Its most advanced experimental drug, SGT-001, is a gene transfer treatment currently in Phase I/II clinical trials, designed to encourage the production of functional dystrophin protein in patients' muscles. The company is also progressing with SGT-003, which represents a next-generation gene transfer therapy intended for DMD. Beyond specific drug candidates, Solid Biosciences is actively developing innovative platform technologies, such as "dual gene expression," a technique that allows for multiple therapeutic genes to be bundled into a single viral vector, and researching new capsid designs. The company maintains a strategic alliance through a collaboration and license agreement with Ultragenyx Pharmaceutical Inc., focusing on the joint development and market introduction of novel gene therapies for Duchenne Muscular Dystrophy. Founded in 2013, Solid Biosciences Inc. conducts its operations from its headquarters in Cambridge, Massachusetts.
Sector: Biological Products, (No Diagnostic Substances)
Industry: Biotechnology
Solid Biosciences Inc.
Trials need funding. See this company's dilution risk and cash position.
- Phase 3Recruiting
A Study of SGT-003 Gene Therapy in Ambulant Males With Duchenne Muscular Dystrophy (IMPACT DUCHENNE)
SGT-003, Placebo
Duchenne Muscular Dystrophy
NCT07160634Enrollment80StartOct 2025Primary CompletionJan 2029est.CompletionJan 2034est. - Phase 1/2Active, not recruiting
Microdystrophin Gene Transfer Study in Adolescents and Children With DMD
SGT-001
Duchenne Muscular Dystrophy
NCT03368742Enrollment12StartDec 2017Primary CompletionNov 2026est.CompletionNov 2026est. - Phase 1/2Recruiting
A Study of SGT-003 Gene Therapy in Duchenne Muscular Dystrophy (INSPIRE DUCHENNE)
SGT-003
Duchenne Muscular Dystrophy
NCT06138639Enrollment60StartMay 2024Primary CompletionMay 2027est.CompletionMay 2031est. - Phase 1Recruiting
A Study of SGT-501 Gene Therapy in Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)
SGT-501
Catecholaminergic Polymorphic Ventricular Tachycardia
NCT07148089Enrollment18StartFeb 2026Primary CompletionJun 2027est.CompletionMay 2031est. - Phase 1Recruiting
A Study of SGT-212 Gene Therapy in Friedreich's Ataxia
SGT-212ORPHAN DRUG
Friedreich's Ataxia (FA)
NCT07180355Enrollment10StartOct 2025Primary CompletionMar 2028est.CompletionFeb 2032est. - ObservationalCompleted
Evaluation of Home Based Assessments on Participants With DMD
Wearable Device, Duchenne Video Assessment (DVA)
Duchenne Muscular Dystrophy
NCT05657938Enrollment17StartOct 2022Primary CompletionApr 2023CompletionApr 2023
| Drug / Therapy | Link | ||
|---|---|---|---|
| Phase 3 | Recruiting | SGT-003, Placebo | NCT07160634 |
| Phase 1/2 | Active, not recruiting | SGT-001 | NCT03368742 |
| Phase 1/2 | Recruiting | SGT-003 | NCT06138639 |
| Phase 1 | Recruiting | SGT-501 | NCT07148089 |
| Phase 1 | Recruiting | SGT-212ORPHAN DRUG | NCT07180355 |
| Observational | Completed | Wearable Device, Duchenne Video Assessment (DVA) | NCT05657938 |