AVE1642 clinical trials
Also written VRDN-001, Veligrotug and AVE1642.
How each study uses AVE1642 is sorted by a rule, right about nine times in ten. Readers can ask us to read every study one by one.Ask us to read each study
Get an email when these change. Save the AVE1642 studies recruiting or about to start — once a week, free: studies that open, close, add sites or post results.
See an example email
Example · made-up studies
Breast cancer · Recruiting: 2 came in, 3 changed
What changed in your saved searches, Oct 31 – Nov 6:
A study of drug A after surgery for early breast cancer
Came in · now Recruiting
Drug B with hormone therapy in advanced breast cancer
Changed
· Sites: 4 added, including Seoul and Busan
· Enrollment: 300 → 450 participants
Exercise during chemotherapy
Now Active, not recruiting
One email a week for all your saved searches. Stop any time.
Approvals
The first approval found in each region, with its record
- United States
- 26 Jun 2026 · LUMVOA · BLA 761530 (FDA, Drugs@FDA)
- European Union
- Not in EMA's list of EU-wide authorisations
From FDA's Drugs@FDA and Purple Book (through openFDA) and the European Medicines Agency, files of Sept 2026 and 27 Oct 2026. National approvals in Europe and other countries are not included. How this is worked out
How studies write it
Studies that test it under each name
Studies by the year they started
7 studies that test it; most in 2024 (2)
| Year | Studies |
|---|---|
| 2006 | 1 |
| 2008 | 1 |
| 2022 | 1 |
| 2023 | 1 |
| 2024 | 2 |
| 2026 | 1 |
By phase
A phase 1/2 study counts in both.
What it is tested for
Each study’s main condition, where its own words name it, so a study counts once.
Who runs them
Industry 7 · Other 0
Coming up
From the study records. Dates are the sponsors’ own estimates and often move.
Reaching primary completion within a year · 1
Studies that test AVE1642.
- Apr 2027An Open-Label Trial of Veligrotug in Participants With Thyroid Eye Disease Who Previously Responded to TeprotumumabPhase 4 · Viridian Therapeutics, Inc.
Studies
Open first, then newest update. How each study uses AVE1642 is read from its arms, and is right about nine times in ten. Ask us to read each study. These are the studies that list it as an intervention; a search of ClinicalTrials.gov also finds studies that mention it only in a description, such as earlier treatment.
Testing it · 7
- An Open-Label Trial of Veligrotug in Participants With Thyroid Eye Disease Who Previously Responded to TeprotumumabNot yet recruitingPhase 4Viridian Therapeutics, Inc.NCT07832136Written as veligrotrug (LUMVOA™)
- An Open-label Study (OLE) for Non-responders of VRDN-001-101 and VRDN-001-301CompletedPhase 3Viridian Therapeutics, Inc.NCT06179875Written as Veligrotug
- A Safety, Tolerability, and Efficacy Study of Veligrotug (VRDN 001) in Participants With Thyroid Eye Disease (TED)CompletedPhase 3Viridian Therapeutics, Inc.NCT05176639Written as Veligrotug
- A Randomized, Controlled, Safety and Tolerability Study of VRDN-001 in Participants With Thyroid Eye Disease (TED)CompletedPhase 3Viridian Therapeutics, Inc.NCT06384547Written as Veligrotug
- An Efficacy, Safety, and Tolerability Study of Veligrotug (VRDN-001), in Participants With Chronic Thyroid Eye Disease (TED)CompletedPhase 3Viridian Therapeutics, Inc.NCT06021054Written as Veligrotug
- Study of AVE1642 (IGF-1R/CD221) in Combination With Fulvestrant (Faslodex®) in Postmenopausal Patients With Advanced Hormono-dependent Breast CancerTerminatedPhase 2SanofiNCT00774878Written as AVE1642
- Study of AVE1642 Anti-IGF1R Monoclonal Antibody in Patients With Advanced Multiple MyelomaCompletedPhase 1SanofiNCT01233895Written as AVE1642
Given beside what is tested · 1 — AVE1642 is usual care or a partner of the new treatment
Codes
What other systems call AVE1642 · ClinicalTrials.gg INT005534
- MeSH (NLM) C545477AVE1642One source NLM
- UNII (FDA) Z9U2SS9ZC8VELIGROTUGConfirmed FDA, NLM
| System | Code | Name there | Checked by |
|---|---|---|---|
| MeSH (NLM) | C545477 | AVE1642 | One source NLM |
| UNII (FDA) | Z9U2SS9ZC8 | VELIGROTUG | Confirmed FDA, NLM |
“Confirmed” means two independent publishers link the code to this drug; “one source”, one does and its name agrees.