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Destroying Cancer at the Speed of Light®

Clinical Study Underway (75 of 100 Patients Treated)
Expected to complete enrollment at the end of 2024
Expected to complete study at the end of 2026


Bullboard - Investor Discussion Forum Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  TLTFF

Theralase Technologies Inc. is a Canada-based clinical-stage pharmaceutical company. The Company is engaged in the research and development of light activated compounds and their associated drug formulations. The Company operates through two divisions: Anti-Cancer Therapy (ACT) and Cool Laser Therapy (CLT). The Anti-Cancer Therapy division develops patented, and patent pending drugs, called... see more

TSXV:TLT - Post Discussion

Theralase Technologies Inc. > New Cutting Edge Paper from Dr. McFarland and Colleagues
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Post by Eoganacht on Aug 14, 2023 6:18pm

New Cutting Edge Paper from Dr. McFarland and Colleagues

One of the problems with light activated photosensitizers is that light only provides limited penetration of tissue. The green light used in the current NMIBC trial, for example, can only penetrate to a depth of 1.5 mm but that is all that is needed to treat NMIBC. For other indications new techniques will need to be developed.

X-rays can penetrate tissue much deeper but can activate currently used photosenstizers to only a limited extent. To get around this limitation researchers have proposed the use of nanoscintillators to mediate the X-rays. The McFarland Group, in collaboration with Dr. Lilge and researchers from the University of Alberta have developed a new nanoscintillator along with a new Ruthenium based photosensitizer to facilitate X-PDT.

The following paper by Chinese and American researchers explains why nanoscintillators are required.

Nanoscintillator-Mediated X-Ray Induced Photodynamic Therapy for Deep-Seated Tumors: From Concept to Biomedical Applications

"The energy of X-rays used in clinical Radiation Therapy is in the range of hundreds of keV to MeV. As a result, most traditional photosensitizers used for cancer PDT cannot be effectively activated by X-rays. In this regard, a physical transducer is required to absorb the X-ray irradiation energy and transfer it to photosensitizers to produce the cytotoxic singlet oxygen (1O2) necessary for tumor destruction. In the classical X-PDT model, this energy transfer is achieved by converting the absorbed x-ray energy into optical photons of the appropriate wavelength that can be absorbed effectively by photosensitizers. These transducers are generally called scintillators and exhibit X-ray excited optical luminescence (XEOL). "

Here is a link to the abstract of Dr. McFarland's new paper:

High Quantum Efficiency Ruthenium Coordination Complex Photosensitizer for Improved Radiation-activated Photodynamic Therapy (radioPDT)

"Traditional external light-based Photodynamic Therapy (PDT)'s application is limited to the surface and minimal thickness tumors because of the inefficiency of light in penetrating deep-seated tumors. To address this, the emerging field of radiationactivated PDT (radioPDT) uses X-rays to trigger photosensitizer-containing nanoparticles (NPs). A key consideration in radioPDT is the energy transfer efficiency from X-rays to the photosensitizer for ultimately generating the phototoxic reactive oxygen species (ROS). In this study, we developed a new variant of pegylated poly-lactic-co-glycolic (PEG-PLGA) encapsulated nanoscintillators (NSCs) along with a new, highly efficient ruthenium-based photosensitizer (Ru/radioPDT). Characterization of this NP via transmission electron microscopy, dynamic light scattering, UV-Vis spectroscopy, and inductively coupled plasma mass-spectroscopy showed an NP size of 120 nm, polydispersity index (PDI) of less than 0.25, high NSCs loading efficiency over 90% and in vitro accumulation within the cytosolic structure of endoplasmic reticulum and lysosome. The therapeutic efficacy of Ru/radioPDT was determined using PC3 cell viability and clonogenic assays. Ru/radioPDT exhibited minimal cell toxicity until activated by radiation to induce significant cancer cell kill over radiation alone. Compared to protoporphyrin IX-mediated radioPDT (PPIX/radioPDT), Ru/radioPDT showed higher capacity for singlet oxygen generation, maintaining a comparable cytotoxic effect on PC3 cells."
Comment by james700 on Aug 15, 2023 7:46am
Here's the question, will this advancement by Dr. McFarland be incorporated into the Theralase ACT division or will this be a separate business venture and compete with tld-1433.
Comment by steamfitter on Aug 15, 2023 8:18am
I believe they are at the start of trials. They will be using X-ray and will require maybe years of proof for the fda just my opinion. 
Comment by Legit62 on Aug 15, 2023 8:48am
if its anything like our treatment, they could be waiting 20 years so nothing to worry about, we have a couple years to go before we hit the big time according to the timelines given to us
Comment by made2last on Aug 15, 2023 8:47am
Hi all; The new tech described is ruthenium based and should fall under the many patents held by Theralase. Thanks; made2last  
Comment by skys1 on Aug 15, 2023 9:56am
Exactly made2last, TLT has so many world-wide, strong patents(Roger described them to me), on their ACT/1433, IMO, they would have to give permission and get a piece of the action on anything close.
Comment by Oilminerdeluxe on Aug 15, 2023 10:37am
Maybe we will receive a little nugget or two worth a smile in the next update. Would be wonderful.
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Investor Presentation

The Road to Saving Lives: Clinical Study Underway

  • Clinical Study with 75 of 100 Patients Treated (Enrollment to be completed by end of 2024, with study completed by end of 2026)
     
  • Ground Floor Investment Opportunity in Multi-Billion Dollar Industry
     
  • Best-in-class treatment for NMIBC (according to interim clinical data)
     
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The Road to Saving Lives: Clinical Study Underway

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  • Ground Floor Investment Opportunity in Multi-Billion Dollar Industry
     
  • Best-in-class treatment for NMIBC (according to interim clinical data)
     
  • NMIBC (Non-Muscle-Invasive Bladder Cancer)
     

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