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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. > J&J is in the metastatic bladder indication
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Post by ScienceFirst on Jun 06, 2023 8:54pm

J&J is in the metastatic bladder indication

J&J could see an opportunity to jv with us to increase its market shares in the bladder indication.


ASCO: Johnson & Johnson's Balversa tops chemotherapy in bladder cancer trial

By Kevin Dunleavy
Jun 5, 2023 02:39pm

In a confirmatory trial win for Johnson & Johnson's Balversa, which was approved in 2019 on an accelerated basis, the treatment outdid chemotherapy in certain bladder cancer patients. (JNJ)

Johnson & Johnson’s Balversa can keep some metastatic bladder cancer patients alive longer than chemotherapy, according to a study of 266 who have fibroblast growth factor receptor (FGFR) gene mutations and had already received checkpoint inhibitors.

In the phase 3 THOR trial, Balversa cut the risk of death by 36% to accomplish its primary objective. It helped extend lives by an average of 12.1 months versus a 7.8-month average for patients on chemotherapy.

The interim results were from cohort 1 of the confirmatory study and were presented Monday at the American Society of Clinical Oncology's (ASCO's) annual meeting in Chicago.

The use of Balversa in this setting supports recommendations for FGFR testing in all patients with metastatic urothelial cancer,” Yohann Loriot, M.D., Ph.D., of the University of Paris-Saclay in France and the principal study investigator, said in a release.

Balversa was approved on an accelerated basis in 2019, becoming the first FGFR inhibitor on the market and prompting then-CEO Alex Gorsky to declare it a potential blockbuster. The daily, oral treatment also was the first approved for bladder cancer that was aimed at a specific genetic biomarker.

FGFR2 and FGFR3 mutations account for roughly 20% of metastatic urothelial carcinomas, which are the most common form of bladder cancer, according to J&J.

J&J did not release results from cohort 2 of the THOR trial, which tested Balversa versus Merck’s Keytruda in patients who have been treated but not with checkpoint inhibitors.

Also at ASCO, J&J also showed final results of the NORSE phase 2 trial that measured Balversa as a solo agent versus a combination of Balversa and J&J’s investigational checkpoint inhibitor cetrelimab as a first-line treatment for patients with metastatic urothelial carcinoma who were ineligible for chemotherapy and had FGFR mutations.

While Balversa alone shrunk tumors in 44.2% of patients, the combo had a 54.5% success rate. Median progression-free survival in the combo arm came in at 11 months versus 5.6 months for Balversa alone. The results were consistent with what J&J showed from the trial two years ago.

Comment by N0taP00p on Jun 06, 2023 10:05pm
So it could take upto 3 years AFTER accelerated approval to get a full approval.  This got an AA in  2019.  I wonder if they were able to charge for it to recover costs over the last 3 years
Comment by ScienceFirst on Jun 06, 2023 11:58pm
The rules clearly stipulate that AA allows one to charge for the treatment to cover costs.  We have no reason to doubt that J&J was not entitled to.
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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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The Road to Saving Lives: Clinical Study Underway

  • Clinical Study with 72 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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Address:
41 Hollinger Road
Toronto, ON M4B 3G4
Canada

Toll Free:
1-866-THE-LASE (843-5273)
Local Phone:
416-699-LASE (5273)

Email:
info@theralase.com

Fax:
416-699-5250