About Us
NeuroThera
NeuroThera is a medical device company building a multi-indication transcranial photobiomodulation (tPBM) platform for the treatment of neurological and psychiatric conditions. Our core technology delivers near-infrared laser energy non-invasively to targeted regions of the prefrontal cortex — stimulating cellular energy metabolism, improving cerebral blood flow, and restoring neural circuit function without drugs or surgery.
What makes NeuroThera’s approach distinctive is its platform architecture. A single device, a single therapeutic mechanism, and a single regulatory foundation support six neurological indications today — with the extensibility to address additional brain conditions as clinical science advances. As our understanding of photobiomodulation deepens, the addressable patient population grows without requiring a new device or a new platform.
Founded in 2015, NeuroThera is built on the scientific and intellectual property foundation of PhotoThera, Inc., whose team conducted the landmark NEST stroke trials — three studies, 1,410 participants — using the identical 808nm wavelength. NeuroThera’s co-founder and CTO, Luis De Taboada, served as VP of R&D at PhotoThera and is widely recognized as one of the world’s foremost experts in transcranial laser therapy.
Our Mission:
“To build the world’s leading transcranial photobiomodulation platform — making non-invasive, drug-free brain therapy a mainstream treatment option for the most prevalent neurological diseases, and extending that reach to new indications as the science of light-based neuromodulation continues to advance.”
Why NeuroThera
- Multi-indication platform: one device, one mechanism, six validated therapeutic targets — MDD, Alzheimer’s Disease, Parkinson’s Disease, TBI, MCI, and Post-Stroke Recovery
- Designed for extensibility: the same core hardware and regulatory foundation can support new indications as clinical evidence develops
- 22 issued patents (20 US, 2 Japan) and 13+ pending applications protecting the platform across indications and configurations
- Three completed clinical studies with positive results; a fourth underway
- Triple biomarker validation: BOLD fMRI, FDG-PET, and EEG — the only tPBM company with all three neuroimaging modalities confirming mechanism and effect
- Zero serious adverse events across all clinical studies
- Leadership team with deep expertise in FDA regulatory pathways, psychiatric medicine, DoD/VA channels, and payer strategy
