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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. > ASCO Presentation - 28% CR at 450 Days
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Post by Eoganacht on Feb 17, 2023 3:32pm

ASCO Presentation - 28% CR at 450 Days

ASCO GU 2023: A Phase II Clinical Study of Intravesical Photo Dynamic Therapy in Patients with BCG-Unresponsive NMIBC (Interim Analysis)
 
(UroToday.com) On the second day of the American Society for Clinical Oncology (ASCO) Genitourinary Cancer Symposium 2023 focussing on urothelial cancer, the Poster Session B: Prostate Cancer and Urothelial Carcinoma included a presentation from Dr. Girish Kulkarni highlighting interim results assessing of intravesical photo dynamic therapy in patients with BCG-unresponsive non-muscle invasive bladder cancer (NMIBC).
 
There is a significant clinical need for novel treatment approaches in patients with BCG-unresponsive, high risk non-muscle invasive bladder cancer. In this abstract, the authors report interim results of a Phase II Clinical Study of Intravesical Photo Dynamic Therapy (PDT) in patients with BCG-Unresponsive Carcinoma In-Situ (CIS) with or without papillary disease.
 
In this trial with a target planned sample size of 125 patients, 42 patients have been enrolled and treated with two Study Treatments (Day 0 and Day 180) consisting of an intravesical instillation of the photosensitizer TLD-1433 (0.70 mg/cm2) followed by activation with a 520 nm intravesical laser under general anesthesia (Study Device TLC-3200) to a total of 90 J/cm2 of laser light (NCT03945162). The primary study outcome assessed was an efficacy endpoint of Complete Response (CR), at any point in time. The secondary outcome was duration of CR at 12 months following an initial CR. Finally, the authors assessed safety as a tertiary endpoint, evaluated by the incidence and severity of Adverse Events, Grade 4 or higher that do not resolve within 450 days post treatment. Patients with a negative cystoscopy and positive cytology were defined as having an indeterminate response (IR), as these patients remain under investigation for lower and upper tract urothelial carcinoma.
 
As of this interim analysis, the authors evaluated the first 42 patients, along with 3 patients treated in a preceding Phase Ib NMIBC clinical study assessing the safety of TLD-1433 PDT, treated using the same parameters, for a total of 45 patients.
 
The interim clinical data demonstrates a 90 day CR of 53% and a duration of response at 360 and 450 days of 29% and 28%, respectively.

Response table.jpg
At this interim evaluation, there have been eight Serious Adverse Events (SAE) identified 2 Grade II (tachycardia, hematuria), 3 Grade III (acute kidney injury, cellulitis), 2 Grade IV (urosepsis, depression/anxiety) and 1 Grade V]. None of the SAEs were deemed to be directly related to the study treatment.
 
Thus, the authors concluded that these interim data support Photo Dynamic Therapy as a viable treatment option for patients with BCG unresponsive CIS (+/- papillary disease) with an acceptable safety profile.
 
Presented by: Girish S. Kulkarni, MD, PhD | Division of Urology, Princess Margaret Cancer Center, University Health Network, University of Toronto
Written by: Christopher J.D. Wallis, University of Toronto Twitter: @WallisCJD during the American Society for Clinical Oncology (ASCO) Genitourinary Cancer Symposium 2023, February 16, 2023 – February 18, 2023.
Comment by DJDawg on Feb 17, 2023 3:59pm
My read is that this was written based off the abstract. I hope the poster has a bit more granularity.
Comment by Eoganacht on Feb 17, 2023 4:35pm
UroToday has more recent data than the abstract.
Comment by DJDawg on Feb 17, 2023 4:42pm
ah yes. my mistake. Glad that they were allowed to present the Nov 29 data.
Comment by Tapps21 on Feb 17, 2023 5:24pm
So please Eog, can you enlighten us as to where this could/may lead us? I appreciate your insight.
Comment by Eoganacht on Feb 17, 2023 6:01pm
Two months ago Ferring Pharmaceuticals received FDA approval for Adstiladrin for high-risk, BCG-unresponsive NMIBC based on a CR rate at 12 months of 23.5%. Today Theralase announced to a symposium of genitourinary oncologists a CR rate at 15 months of 28% for the same indication. TLD1433 pdt has higher efficacy, a more enduring response, and better results are likely on the way. On May ...more  
Comment by Tapps21 on Feb 17, 2023 6:14pm
Thanks . Always a pleasure to read your I depth, positive post. 
Comment by BlueFranky on Feb 17, 2023 6:14pm
Thanks Eog! that sure paints a favorable picture ;-)
Comment by 99942Apophis on Feb 17, 2023 6:15pm
Very true Eoganacht not only that it wasn't part of the for Urologist conversations but pretty well anyone outside of shareholders for this stock.  I see here a strong effort by this company to let health care people associated with NMIBC cancer treatment that Theralase is the new friendly kid on the block! After the May AUA presentation I think news will be released to local and ...more  
Comment by Rumpl3StiltSkin on Feb 18, 2023 10:44am
Nice Eoga, I wish Ferrin was publicly traded so we could all see the effect on their SP of FDA approval. TLT's 1433 should be a bit cheaper, is less toxic, is standalone, and requires fewer treatments that are less invasive... :-)
Comment by CancerSlayer on Feb 20, 2023 2:40am
  To add....viral-vector gene therapies are certainly not harmless & they come with a hefty monetary & physical price....in the Adstiladrin trial, 34% of patients had interruptions in their treatments due to adverse reactions.  It is also a drug that should not be taken by those who are immunosuppressed.   I believe their reported 23.5% durable response (DR) does ...more  
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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)
     
  • NMIBC (Non-Muscle-Invasive Bladder Cancer)
     

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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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