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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

Comment by ScienceFirston Nov 30, 2022 8:33pm
309 Views
Post# 35141623

RE:Possible TR @450-days of 70%+

RE:Possible TR @450-days of 70%+I found this interesting statement in ImmunityBio's news release on their BCG-Unresponsive trial.


ImmunityBio Announces Over 24 Months Median Duration of Complete Remission, with 100% NMIBC CIS Patient Survival, Setting a New ‘Magnitude of Benefit’ in Patients with BCG Unresponsive Bladder Cancer

...

In addition, for patients with papillary disease, a disease-free survival rate at 18 months of 53%, which more than doubles the 25% rate published by the International Bladder Cancer Group as clinically meaningful


So fair to assume that we already reach this IBCG target of 25%.  And that we could surpass the "53%" of ImmunityBio.  N-803 is used in combo with BCG.  And its treatment is much complicated than ours:


Drug: N-803 and BCG (Phase 2)
BCG and N-803 will be mixed together (with saline) and administered via intravesical instillation weekly for 6 consecutive weeks (induction). After the first disease assessment, eligible patients will receive either a 3-week maintenance course or a 6-week re-induction course (second treatment period) at Month 3. Eligible patients will continue to receive maintenance treatment in the third treatment period at Months 6, 9, 12, and 18. Eligible patients have the option to receive maintenance treatment in the fourth treatment period at Months 24, 30, and 36.



Dr. Lerner went on to present results from the recent QUILT 3032 trial, where patients with NMIBC were randomized to 50 mgBCG plus 40 ug N-803 intravesically weekly x 6 induction or re-induction x6 with up to 2 years maintenance, with an option to extend. The 12 and 24 month durable complete remission in cohort A (CIS) was 60% and 52%, respectively.

Note that our MSAB is Dr. Kamat.  He's also the founder of IBCG. ... ;-)

In addition, for patients with papillary disease, a disease-free survival rate at 18 months of 53%, which more than doubles the 25% rate published by the International Bladder Cancer Group as clinically meaningful
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