Lumvoa Injection
Product Images NDC 85166-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lumvoa (NDC 85166-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viridian Therapeutics, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Figure (Vel03 0002 01)

A line graph showing the change in proptosis from baseline (in mm) over 15 weeks, comparing Lumvoa (veligrotug) injection versus placebo. The x-axis represents time points (Baseline, Weeks 3, 6, 9, 12, and 15), and the y-axis shows proptosis change from baseline. Lumvoa shows a greater decrease in proptosis over time compared to placebo.*

FDA Label Image

Figure (Vel03 0002 02)

A line graph depicting proptosis change from baseline (in millimeters) over 15 weeks, comparing Lumvoa (veligrotug, 50 mg/mL injection) versus placebo. The y-axis shows proptosis change, and the x-axis shows time points from baseline to week 15. Lumvoa shows a greater decrease in proptosis over time compared to placebo.*

FDA Label Image

Principal Display Panel (500 mg/10 mL Carton Label)

Packaging label for Lumvoa (veligrotug-vvze) injection, 500 mg/10 mL (50 mg/mL), for intravenous use only. The label indicates a 10 mL single-dose vial with instructions to dilute prior to use and discard unused portions. It includes storage instructions to keep refrigerated at 2°C to 8°C and warnings not to freeze or shake. Manufactured by Viridian Therapeutics, Inc., located in Waltham, MA.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.