
*The presence of at least 3 medium drusen (>63 μm and ≤125 μm in diameter), or large drusen (>125 μm in diameter), or non-central geographic atrophy.

Valeda™ PBM LIGHTSITE III clinical trial met the predetermined primary efficacy endpoint at Month 212†
84% of Valeda™ PBM–treated patients improved or maintained vision at ~2 years compared to baseline3,4†
More than 60% of Valeda™ PBM–treated patients experienced ≥1-line vision improvement at about 2 years compared to baseline3,4†
† n=98 subjects and 145 eyes
LIGHTSITE III Pivotal Trial Design
LIGHTSITE III evaluated the efficacy and safety of Valeda™ PBM in a 24-month, double-masked, sham-controlled, parallel design, prospective, randomized, multi-center trial.4,5
98 patients (145 eyes) aged ≥50 years with ETDRS BCVA letter score between 50 and 75 and a diagnosis of dry AMD defined by the presence of drusen and/or nonfoveal center GA were randomized at a 2:1 ratio into 2 treatment groups.4
Primary efficacy endpoint: Mean BCVA change from baseline to Month 13 or Month 21. Primary safety endpoint: Mean change from baseline to Month 13 or Month 24.4
Consistent safety in multiple clinical trials

0 reports of phototoxicity in 3
LIGHTSITE trials2
of patients did not report
eye pain4
Dilation free. Anesthesia free. Speculum free. Injection free.4

Treatment regimen consists of 54 applications administrated in 6 courses over 2 years
Valeda™ PBM applies 3 science-backed wavelengths to upregulate cellular energy production6,7

Increases nitric oxide synthesis and vasodilation which can improve local oxygenation and nutrient delivery6

Promotes O2 binding (CuB), stimulates metabolic activity (ATP), and inhibits inflammation and cell death7

Drives electron transfer (CuA), stimulates metabolic activity (ATP), and inhibits inflammation and cell death7

The retina is rich in mitochondria, and mitochondrial dysfunction is a known cause of vision loss in dry AMD.

Cytochrome c oxidase (CcO) is a key photoacceptor in the mitochondrial electron transport chain.

Valeda™ PBM wavelengths activate CcO, enhancing electron transport and mitochondrial adenosine triphosphate (ATP) production, the cell’s major source of energy.
Valeda™ PBM is the first and only FDA-authorized treatment for early and intermediate dry AMD1
84% of Valeda™ PBM–treated patients improved or maintained vision at ~2 years compared to baseline3,4*
Dilation free, speculum free, anesthesia free, and injection free4
