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NCT05176639: THRIVE

A Safety, Tolerability and Efficacy Study of Veligrotug (VRDN 001) in Healthy Volunteers and Participants With Thyroid Eye Disease (TED) ( THRIVE )

Completed Phase 3 Last updated 18 July 2025
What this trial tests

Phase 3 trial testing VRDN-001 Phase 3 Cohort (THRIVE) in Thyroid Eye Disease in 113 participants. Completed in 27 March 2025.

Timeline
3 December 2021
Primary endpoint
15 July 2024
27 March 2025

Quick facts

Lead sponsorViridian Therapeutics, Inc.
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment113
Start date3 December 2021
Primary completion15 July 2024
Estimated completion27 March 2025
Sites53 locations across France, United Kingdom, Germany, Poland, Australia, United States, Spain

Drugs / interventions tested

Conditions studied

Sponsor

Viridian Therapeutics, Inc. — full company profile →

Who can join

18 and older, any sex, with Thyroid Eye Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The investigational drug, veligrotug (VRDN-001), is a monoclonal antibody that inhibits the activity of a cell surface receptor called insulin-like growth factor-1 receptor (IGF-1R). Inhibition of IGF-1R may help to reduce the inflammation and associated tissue swelling that occurs in patients with thyroid eye disease (TED). The primary objective of this clinical trial is to establish the safety, tolerability, and efficacy of veligrotug, and the pharmacokinetic (PK) and pharmacodynamic (PD) profiles of veligrotug in active TED patients who received 10 mg/kg.

Publications & conference data

8 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Angiogenic signaling pathways and anti-angiogenic therapy for cancer.
    Liu ZL, Chen HH, Zheng LL, Sun LP, et al · · 2023 · cited 808× · PMID 37169756 · DOI 10.1038/s41392-023-01460-1
  2. From geroscience to precision geromedicine: Understanding and managing aging.
    Kroemer G, Maier AB, Cuervo AM, Gladyshev VN, et al · · 2025 · cited 139× · PMID 40250404 · DOI 10.1016/j.cell.2025.03.011
  3. Antibodies to watch in 2025.
    Crescioli S, Kaplon H, Wang L, Visweswaraiah J, et al · · 2025 · cited 87× · PMID 39711140 · DOI 10.1080/19420862.2024.2443538
  4. The changing landscape of thyroid eye disease: current clinical advances and future outlook.
    Moledina M, Damato EM, Lee V. · · 2024 · cited 37× · PMID 38374366 · DOI 10.1038/s41433-024-02967-9
  5. Understanding Pathogenesis Intersects With Effective Treatment for Thyroid Eye Disease.
    Smith TJ. · · 2022 · cited 34× · PMID 36346686 · DOI 10.1210/clinem/dgac328
  6. Angiogenesis and targeted therapy in the tumour microenvironment: From basic to clinical practice.
    Yang S, Fang Y, Ma Y, Wang F, et al · · 2025 · cited 22× · PMID 40268524 · DOI 10.1002/ctm2.70313
  7. A Comprehensive Review of Thyroid Eye Disease Pathogenesis: From Immune Dysregulations to Novel Diagnostic and Therapeutic Approaches.
    Kulbay M, Tanya SM, Tuli N, Dahoud J, et al · · 2024 · cited 18× · PMID 39519180 · DOI 10.3390/ijms252111628
  8. Targeting the Neonatal Fc Receptor in Autoimmune Diseases: Pipeline and Progress.
    Gjølberg TT, Mester S, Calamera G, Telstad JS, et al · · 2025 · cited 10× · PMID 40156757 · DOI 10.1007/s40259-025-00708-2

Verify or expand the search:

Other recruiting trials for Thyroid Eye Disease

Currently open trials in the same condition.

Other Viridian Therapeutics, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05176639.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing