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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 Photo Dynamic Compounds (PDCs) and activates them with patent pending laser technology to destroy specifically targeted cancers, bacteria and viruses. The CLT division is responsible for the Company’s medical laser business. The Cool Laser Therapy division designs, develops, manufactures and markets super-pulsed laser technology indicated for the healing of chronic knee pain. The technology has been used off-label for healing numerous nerve, muscle and joint conditions. The Company develops products both internally and using the assistance of specialist external resources.


TSXV:TLT - Post by User

Post by Eoganachton Jan 15, 2023 9:28pm
551 Views
Post# 35224665

FDA to rule on BLA for N-803 + BCG for NMIBC by May 23, 2023

FDA to rule on BLA for N-803 + BCG for NMIBC by May 23, 2023If the FDA rules favourably for ImmunityBio's BLA in May what will this mean for TLD1433 pdt? The following quote about the combination N-803 + BCG trial results is from: https://www.precisionvaccinations.com/vaccines/n-803-plus-bcg-vaccine-therapy

"On December 27, 2022, an editorial from urological cancer experts from Memorial Sloan Kettering Cancer Center stated: "The efficacy and minimal toxicity of this combination represents a major advance for the care of patients with BCG-unresponsive NMIBC, and the authors should be congratulated. In addition, this promising combination offers a potential alternative to cystectomy and may allow us to move beyond single-arm studies toward randomized phase 3 trials against other novel therapies.""

How do the results of our current trials compare? ImmunityBio's Trial has been divided into 3 cohorts - Cohorts A, B and C. The results of Cohorts A and C can be directly compared to our trial, as Cohort A represents CIS with Ta/T1papillary disease and Cohort C represents CIS without Ta/T1 papillary disease. Our trial is for CIS with or without Ta/T1 papillary disease, so our trial is directly comparable to the results of Cohorts A & C taken together.

In Cohort A 37 of 82 evaluable patients, or 45% attained a CR at 12 months
In Cohort A 27 of 82 evaluable patients, or 32% attained a CR at 18 months

Cohort B didn't do so well. Evaluation of these10 patients was discontinued at 6 months as only one patient had attained a CR. But to do a proper comparison with our trial the 10 unresponsive patients should be taken into account.

In the combination of Cohorts A & B 37 of 92 patients, or 40% attained a CR at 12 months.
In the combination of Cohorts A & B 27 of 92 patients, or 29% attained a CR at 18 months.

So far, with 12 undertreated patients out of 26 evaluated Theralase has achieved a 28% CR rate at 12 months. This number should improve dramatically as the trial continues.

Also of note is how quickly the CR rate of N-803 + BCG dropped between 12 and 18 months - a drop of 11%. TLD1433 pdt patients are much more likely to maintain their CR over time.

Also, as many have mentioned, TLD1433 is a standalone treatment, and N-803 is dependent on BCG, which is in short supply. TLD1433 is also extremely safe and only requires 2 treatments. N803/BCG has the same safety issues as BCG and requires 6 treatments.

https://evidence.nejm.org/doi/full/10.1056/EVIDoa2200167
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