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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 )
Phase 3 trial testing VRDN-001 Phase 3 Cohort (THRIVE) in Thyroid Eye Disease in 113 participants. Completed in 27 March 2025.
15 July 2024
Quick facts
| Lead sponsor | Viridian Therapeutics, Inc. |
|---|---|
| Phase | Phase 3 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | treatment |
| Enrollment | 113 |
| Start date | 3 December 2021 |
| Primary completion | 15 July 2024 |
| Estimated completion | 27 March 2025 |
| Sites | 53 locations across France, United Kingdom, Germany, Poland, Australia, United States, Spain |
Drugs / interventions tested
- VRDN-001 Phase 3 Cohort (THRIVE) — full drug profile →
- VRDN-001 Placebo — full drug profile →
Conditions studied
- Thyroid Eye Disease — all drugs for Thyroid Eye Disease →
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):
-
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 -
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 -
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 -
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 -
Understanding Pathogenesis Intersects With Effective Treatment for Thyroid Eye Disease.
Smith TJ. · · 2022 · cited 34× · PMID 36346686 · DOI 10.1210/clinem/dgac328 -
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 -
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 -
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:
- PubMed search for NCT05176639
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Thyroid Eye Disease
Currently open trials in the same condition.
- NCT07423013 — Evaluating the Efficacy and Safety of Teprotumumab N01 in Patients With Thyroid Eye Disease. · NA · recruiting
- NCT07113262 — A Clinical Study to Evaluate the Efficacy and Safety of IBI311 in Subjects With Inactive Thyroid Eye Disease · Phase 3 · recruiting
- NCT06557850 — A Trial Investigating Lu AG22515 in Adult Participants With Moderate-to-Severe Thyroid Eye Disease · Phase 1 · active not recruiting
- NCT06625411 — An Efficacy, Safety, and Tolerability Study of VRDN-003 in Participants With Active Thyroid Eye Disease (TED) · Phase 3 · active not recruiting
- NCT06625398 — An Efficacy, Safety, and Tolerability Study of VRDN-003 in Participants With Chronic Thyroid Eye Disease (TED) · Phase 3 · active not recruiting
Other Viridian Therapeutics, Inc. trials
Trials by the same sponsor.
- NCT06625411 — An Efficacy, Safety, and Tolerability Study of VRDN-003 in Participants With Active Thyroid Eye Disease (TED) · Phase 3 · active not recruiting
- NCT06625398 — An Efficacy, Safety, and Tolerability Study of VRDN-003 in Participants With Chronic Thyroid Eye Disease (TED) · Phase 3 · active not recruiting
- NCT06384547 — A Randomized, Controlled, Safety and Tolerability Study of VRDN-001 in Participants With Thyroid Eye Disease (TED) · Phase 3 · completed
- NCT06179875 — An Open-label Study (OLE) for Non-responders of VRDN-001-101 and VRDN-001-301 · Phase 3 · completed
- NCT06021054 — An Efficacy, Safety, and Tolerability Study of Veligrotug (VRDN-001), in Participants With Chronic Thyroid Eye Disease ( · Phase 3 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05176639 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Viridian Therapeutics, Inc.
- Last refreshed: 18 July 2025
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