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VRDN US Equity

Viridian Therapeutics, Inc.\DEHealth Care · Pharmaceutical Preparations · CIK 1590750 · FY ends Dec 31
$23.93
+0.84 (+3.64%)
USD · as of 2026-08-18 · marketstack
8 registered studies · 3 active

Studies where VRDN 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.

8 interventional · 4 with posted results

Held by 10 tracked-famous managers (Point72 Asset Management, L.P., Balyasny Asset Management L.P., D. E. Shaw & Co., Inc., Schonfeld Strategic Advisors LLC, RENAISSANCE TECHNOLOGIES LLC, +5 more) · FINRA short interest 11.3 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionUpdated
A Safety and Tolerability Study of VRDN-003 in Participants With Thyroid Eye Disease (TED)NCT06812325Treatment Emergent Adverse Event (TEAE) incidence rate through Week 24Randomized · Triple-masked · TreatmentPhase 3Active, not recruitingDrug: VRDN-003, PlaceboThyroid Eye Disease (TED)3202026-04-22actual2026-05-22
An Efficacy, Safety, and Tolerability Study of VRDN-003 in Participants With Chronic Thyroid Eye Disease (TED)NCT06625398Title: Proptosis Responder Rate in the most proptotic eye as measured by exophtalmometerRandomized · Triple-masked · TreatmentPhase 3Active, not recruitingDrug: VRDN-003, PlaceboThyroid Eye Disease2042026-03-04actual2026-08-18
An Efficacy, Safety, and Tolerability Study of VRDN-003 in Participants With Active Thyroid Eye Disease (TED)NCT06625411Proptosis Responder Rate in the most proptotic eye as measured by exophtalmometerRandomized · Triple-masked · TreatmentPhase 3Active, not recruitingDrug: VRDN-003, PlaceboThyroid Eye Disease1322026-02-12actual2026-08-18
A Safety, Tolerability and Pharmacokinetics Study of VRDN-003 in Participants With Thyroid Eye Disease (TED)NCT07155668Treatment Emergent Adverse Event (TEAE) incidence rateRandomized · Open-label · TreatmentPhase 3CompletedDrug: VRDN-003 · Device: AutoinjectorThyroid Eye Disease872026-05-28actual2026-06-25
A Randomized, Controlled, Safety and Tolerability Study of VRDN-001 in Participants With Thyroid Eye Disease (TED)NCT06384547results2026-08-13Number of Participants With Treatment-emergent Adverse Events (TEAEs) Through Week 15Randomized · Double-masked · TreatmentStudy Protocol · Statistical Analysis PlanPhase 3CompletedDrug: VeligrotugThyroid Eye Disease2312025-05-01actual2026-08-13
An Open-label Study (OLE) for Non-responders of VRDN-001-101 and VRDN-001-301NCT06179875results2026-08-14Proptosis Responder Rate (PRR) in the Most Proptotic Eye as Measured by ExophthalmometerOpen-label · TreatmentStudy Protocol · Statistical Analysis PlanPhase 3CompletedDrug: VeligrotugThyroid Eye Disease1392025-04-25actual2026-08-14
An Efficacy, Safety, and Tolerability Study of Veligrotug (VRDN-001), in Participants With Chronic Thyroid Eye Disease (TED)NCT06021054results2026-08-13Proptosis Responder Rate (PRR) in the Most Proptotic Eye as Measured by ExophthalmometerRandomized · Triple-masked · TreatmentStudy Protocol · Statistical Analysis PlanPhase 3CompletedDrug: Veligrotug, PlaceboThyroid Eye Disease1882024-11-04actual2026-08-13
A Safety, Tolerability, and Efficacy Study of Veligrotug (VRDN 001) in Participants With Thyroid Eye Disease (TED)NCT05176639results2026-08-13Proptosis Responder Rate (PRR) in the Study Eye As Measured by ExophthalmometerRandomized · Triple-masked · TreatmentStudy Protocol · Statistical Analysis PlanPhase 3CompletedDrug: Veligrotug, PlaceboThyroid Eye Disease1132024-07-15actual2026-08-13

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