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SLDB US Equity

Solid Biosciences Inc.Health Care · Biological Products, (No Diagnostic Substances) · CIK 1707502 · FY ends Dec 31
$9.08
-0.02 (-0.22%)
USD · as of 2026-08-18 · marketstack
6 registered studies · 5 active

Studies where SLDB is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

5 interventional · 1 observational

Held by 11 tracked-famous managers (CITADEL ADVISORS LLC, Point72 Asset Management, L.P., D. E. Shaw & Co., Inc., Balyasny Asset Management L.P., SUSQUEHANNA INTERNATIONAL GROUP, LLP, +6 more) · FINRA short interest 16.2 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
A Study of SGT-003 Gene Therapy in Ambulant Males With Duchenne Muscular Dystrophy (IMPACT DUCHENNE)NCT07160634Change From Baseline in Time to Rise (TTR) from Supine Velocity (rise/s) at Day 540Randomized · Quadruple-masked · TreatmentPhase 3RecruitingDrug: SGT-003, PlaceboDuchenne Muscular Dystrophy80Jan 2029≤ 896 d2026-08-13
A Study of SGT-212 Gene Therapy in Friedreich's AtaxiaNCT07180355Incidence and Severity of Treatment Emergent Adverse Events (TEAEs)Non-randomized · Open-label · TreatmentPhase 1RecruitingDrug: SGT-212Friedreich's Ataxia (FA)102028-03-21in 580 d2026-08-17
A Study of SGT-501 Gene Therapy in Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)NCT07148089Number of Participants with Treatment-Emergent Adverse Event (TEAEs)s through Day 360Non-randomized · Open-label · TreatmentPhase 1RecruitingDrug: SGT-501Catecholaminergic Polymorphic Ventricular Tachycardia18Jun 2027≤ 315 d2026-08-10
A Study of SGT-003 Gene Therapy in Duchenne Muscular Dystrophy (INSPIRE DUCHENNE)NCT06138639Incidence of treatment-emergent adverse events (AEs)Non-randomized · Open-label · TreatmentPhase 1/2RecruitingGenetic: SGT-003Duchenne Muscular Dystrophy602027-05-06in 260 d2026-07-08
Microdystrophin Gene Transfer Study in Adolescents and Children With DMDNCT03368742Number of Participants with Treatment Emergent Adverse Events (TEAEs)Non-randomized · Open-label · TreatmentPhase 1/2Active, not recruitingGenetic: SGT-001Duchenne Muscular Dystrophy122026-10-15in 57 d2026-08-10
Evaluation of Home Based Assessments on Participants With DMDNCT05657938observationalWearable sensor device complianceCompletedDevice: Wearable Device · Other: Duchenne Video Assessment (DVA)Duchenne Muscular Dystrophy172023-04-04actual2023-08-14

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19