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 software platform supporting six neurological indications, 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. 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
The numbers

Major Depressive Disorder

20,000,000 +
Cases in USA
1 in 10
Americans take antidepressants
14 %
take drugs for 10+ years