Join today and have your say! It’s FREE!

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.
Please Try Again
{{ error }}
By providing my email, I consent to receiving investment related electronic messages from Stockhouse.

or

Sign In

Please Try Again
{{ error }}
Password Hint : {{passwordHint}}
Forgot Password?

or

Please Try Again {{ error }}

Send my password

SUCCESS
An email was sent with password retrieval instructions. Please go to the link in the email message to retrieve your password.

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.
Quote  |  Bullboard  |  News  |  Opinion  |  Profile  |  Peers  |  Filings  |  Financials  |  Options  |  Price History  |  Ratios  |  Ownership  |  Insiders  |  Valuation

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 ScienceFirston May 10, 2022 8:03pm
377 Views
Post# 34672446

BCG + Keytruda

BCG + KeytrudaQuite amazing how BCG can still be allowed, despite so high rate of recurences!

I wouldn't be surprized if TLD-1433 become the new "BCG" in terms of usage, given our much higher efficacy, lower number of doses, low toxicity.

Below, Merck is using 2 of its own product;  BCG and Keytruda.  They have nothing to lose.  But just imagine the cost of this treatment.  It can only help us set a price close to this combo.

MP54-02: Two-Year Efficacy Follow-Up of a Phase I trial of Intravesical Bacillus Calmette-Gurin (BCG) Combined with Intravenous Pembrolizumab (Keytruda) in Recurrent or Persistent High-Grade Non-Muscle-Invasive Bladder Cancer after Previous Bacillus Calmette-Gurin (BCG) Treat

Monday, May 16, 2022 8:45 AM to 10:00 AM

Information Authors: Shaheen Alanee, Detroit, MI, Jazzmyne Montgomery*, Springfield, IL, Sherjeel Sana, Milwaukee, WI, Ahmed El-Zawahry, Toledo, OH, James Peabody, Tiffany Pearce, Nicole Adams, Mustafa Deebajah, Detroit, MI, Danuta Dynda, Kara Babaian, Jane Crabtree, Kristin Delfino, Springfield, IL, Kevin McVary, Maywood, IL, Kathy Robinson, Krishna Rao, Springfield, IL   

Introduction:

We conducted the first phase I dose-escalation trial (NCT02324582) of intravesical Bacillus Calmette-Gurin (BCG) in combination with systemic pembrolizumab in patients with high-grade non-muscle-invasive bladder cancer (HGNMIBC) who had persistent or recurrent disease after prior intravesical therapy with BCG. To assess disease-free survival (DFS) and overall survival (OS), patients from this phase I trial NCT02324582 were followed for approximately 2 years. 

Methods:

Eighteen patients were consented for the study, five of whom were screen failures. Six doses of pembrolizumab were administered every 3 weeks over 16 weeks concurrently with six weekly doses of BCG beginning at week 7. Patient safety was evaluated from the time of consent through 30 days following pembrolizumab treatment and was reported previously. Clinical activity was determined using cystoscopy and cytology with biopsy of suspicious lesions. 

Results:

At the updated data cutoff (10/10/2021), the median age of the 13 patients treated was 73 years, 11 were males. Most patients were Caucasians (92.3%). Initial bladder cancer pathology was pT1 in 9 (69.2%), pTa in 3 (23.1%), and carcinoma in situ (CIS) in 1 (7.7%). The pathologic disease stage immediately prior to enrollment (after restaging transurethral resection) was pTa in 6 (46.2%), CIS in 6 (46.2%), and pT1 in 1 (7.7%). At 12 months, the DFS and OS were 69.23%, and 92.31% respectively. At 24 months, the DFS and OS were 38.46% and 92.31% respectively. The attached graph depicts disease free survival rate in our patient population. 

Conclusions:

We have now established safety and present 2 year response data on our group of subjects treated with BCG combined with intravenous pembrolizumab in patients with recurrent or persistent HGNMIBC. A phase III trial is currently recruiting subjects to test the efficacy of this combination in HGNMIBC (KEYNOTE-676). 

Source of Funding: Merck

<< Previous
Bullboard Posts
Next >>