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Lumvoa

Veligrotug-vvze
Insulin-like Growth Factor-1 Receptor (IGF-1R) Inhibitors
Injection

Lumvoa is an FDA approved treatment for Thyroid Eye Disease (TED), regardless of disease activity or duration. It is an insulin-like growth factor-1 receptor (IGF-1R) inhibitor that targets the underlying disease pathway involved in orbital inflammation and tissue remodeling associated with TED. As a new therapeutic option in this rare autoimmune condition, Lumvoa has the potential to reshape the treatment landscape for patients with thyroid eye disease. For clinical trial and first-to-file teams, monitoring its market adoption, exclusivity timeline, and availability will be important, as it may emerge as a relevant comparator in ophthalmology and autoimmune disease studies.

Approval Date
26-Jun-26
Data Exclusivity Expiry
26-Jun-30
Market Exclusivity Expiry
26-Jun-38
Commercial snapshot

Market performance & projections

Revenue ($M)
NA
CAGR (%)
NA
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
25
2027
256
2028
532
2029
718
2030
792
2031
874
2032
958
Molecule profile

Details & specifications

Molecule
Veligrotug-vvze
Innovator
VIRIDIAN THERAPEUTICS INC
Dosage Form
Injection
Strength
500 mg/10 mL
Therapeutic Category
Insulin-like Growth Factor-1 Receptor (IGF-1R) Inhibitors
Usage
To treat thyroid eye disease
Good to know

Frequently asked questions

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Intelligence you can file on

Verified regulatory data
Milestones tracked against primary FDA sources and refreshed continuously.
Analyst-built projections
Seven-year sales outlooks modeled by our pharma intelligence team.
First-to-file focus
Exclusivity windows framed around the decisions generics teams actually make.
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