Therapeutics

INTELLIGENT MATERIAL
NOVAVERATX · THERAPEUTICS

Generate light
where the disease is.

Intelligent Material converts tissue-penetrating energy into localized light inside or adjacent to diseased tissue, creating a platform for photodynamic therapy, imaging and other energy-driven interventions.

HOW NOVAVERATX WORKS Invisible near-infrared light in. Therapeutic light made at the target. SKIN TISSUE DEEP TISSUE ① 980 nm near-infrared in passes through skin and tissue ② Crystals convert it into visible light, locally ③ Drug activated at tumor photosensitizer switches on
Illustrative. Near-infrared travels deeper into tissue than visible light.
The crystals make the treatment light where it is needed.
Photodynamic therapy works. Light delivery is the problem.

Conventional photodynamic therapy requires visible light to activate a photosensitizer. That makes surface and accessible disease comparatively straightforward, but visible light penetrates tissue poorly. The NovaVeraTx concept changes the geometry: deliver energy that penetrates farther, then convert it into the required light at the target.

This “inside-out” approach is the core of the program. The uploaded platform materials describe both infrared and X-ray activation, with Intelligent Material serving as the local energy-conversion element.

FROM THE ARCHIVE

The PDT story, told by the people who built it.

A Discovery feature with Steve Hahn, Joe Friedberg and Josh Collins traces the early photodynamic-therapy work that led to today’s effort to generate the activating light closer to the disease.

HOW IT WORKS

Energy is delivered from outside.
Light is generated on the inside.

01

Tissue-penetrating trigger

Near-infrared light, X-rays or another selected energy source reaches the target region.

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03

Localized light

Emission is generated at or near the disease instead of relying on surface illumination.

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04

Photosensitizer activation

The emission is matched to the photosensitizer absorption band.

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05

Therapeutic effect

Activated photosensitizer transfers energy to molecular oxygen, generating cytotoxic reactive oxygen species.

Inside-out light generation concept
The central idea: move the light source from outside the body to the target itself by converting penetrating energy locally.
Why combining weak energy matters

Imagine trying to break down a door by throwing a billion loose toothpicks at it, one at a time. Nothing useful happens. Glue three million of those toothpicks together and now you have something that can act like a ram.

The analogy is not literal photon counting, but the idea is similar. Near-infrared light passes through tissue well, yet each infrared photon carries too little energy to activate most photosensitizers. Our rare-earth crystals can absorb several of those lower-energy photons and emit one higher-energy photon locally, creating the wavelength needed inside tissue to activate a photosensitizer, a light-triggered drug, or another photochemical function.

THE PLATFORM

One materials concept.
Multiple activation pathways.

01

Infrared-activated PDT

Rare-earth crystals can absorb near-infrared excitation and emit shorter-wavelength light selected to overlap a photosensitizer. The concept is aimed at moving activation deeper than direct visible illumination.

NIR → visible
02

X-ray-activated PDT

Scintillating or energy-converting materials can convert ionizing radiation into localized optical emission, creating another path to activate photosensitizers at depth.

X-ray → light
03

Biodegradable materials

The program includes biodegradable hafnium-oxide concepts, alongside rare-earth hosts, for applications where the material should perform its function and then clear or degrade.

HfO₂ platform
04

Localized delivery

Potential embodiments include intratumoral delivery, implantable depots, hydrogels, targeted particles, brachytherapy-adjacent systems and fiber-optic or wearable activation hardware.

localize + activate

The uploaded program deck describes intratumoral/implantable localization, degradable embodiments, wearable activation systems and endoscopic/fiber-optic delivery concepts.

ENGINEERING THE RESPONSE

The therapy starts with the crystal.

We can tune the material to the energy source, photosensitizer and delivery route rather than forcing one material into every indication.

Host latticeGadolinium, yttrium, hafnium and other engineered hosts
Rare-earth compositionEr, Yb, Tm, Ho and other activator/sensitizer combinations
Emission spectrumMatch output to the absorption band of the selected photosensitizer
Particle architectureSize, morphology, core/shell design and surface chemistry
Delivery biologyLocalized depots, targeted systems, coatings and biodegradable embodiments
Activation hardwareVCSELs, laser diodes, fiber optics, X-ray systems and implantable sources
SCIENTIFIC LINEAGE

This program did not start yesterday.

2002

Early SPIE work in pleural PDT

Joseph S. Friedberg was a co-author on the SPIE paper The ratio of the spherical and flat detectors at tissue surfaces during pleural photodynamic therapy, part of the early Penn/Jefferson clinical and dosimetry work around pleural PDT.

View the SPIE paper →
2006

Measuring light in human pleural PDT

Friedberg also co-authored the SPIE study Diffuse reflectance spectra measured in vivo in human tissues during Photofrin-mediated pleural photodynamic therapy, extending the focus on understanding and controlling light delivery in patients.

Read the paper →
NOW

Move the light source to the disease

NovaVeraTx builds directly on that progression: clinical PDT and dosimetry, then Sunstones infrared-to-visible activation, then X-ray-to-visible activation, and now a broader Intelligent Material platform engineered around the energy source, material, photosensitizer and delivery system as one integrated therapeutic architecture.

LEGACY PRECLINICAL PROGRAM

A signal worth pursuing.

Program materials supplied by IMS summarize both ex vivo lung-cancer experiments and an in vivo murine mesothelioma study using an infrared/material/photosensitizer combination. These results are preclinical, not evidence of clinical efficacy.

8/10
animals in the treatment group were reported with no palpable tumor at day 18.
80%
reported survival for the complete combination group over the observation period.
Legacy preclinical tumor regression chart
Legacy program summary: murine mesothelioma tumor-volume study.
Legacy preclinical survival chart
Legacy program summary: 90-day survival outcome.

These values are taken from the uploaded program deck.

RESEARCH DIRECTIONS

Where local energy conversion could matter.

Brain / glioblastoma
Head & neck
Lung / esophageal
Liver / pancreatic
Prostate
Melanoma
Closed-space infections
Respiratory disease

These are research targets and platform-expansion concepts described in the supplied materials, not approved indications.

COMMERCIALIZATION

IMS intellectual property.
NovaVeraTx development.

Intelligent Material Solutions develops and owns intellectual property around energy-converting materials. NovaVera Corporation is the commercialization arm for the technology, with NovaVeraTx focused on therapeutics.

The objective is to combine materials science, optical delivery, pharmacology and clinically experienced PDT leadership into one development program.

Discuss a therapeutic program