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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. > Dr. Chamie Interview - Quilt 3.032 study (N-803 + BCG)
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Post by Eoganacht on Apr 20, 2023 1:11pm

Dr. Chamie Interview - Quilt 3.032 study (N-803 + BCG)

It turns out that this treatment achieved a 2 year CR rate of 35%.

I believe TLD1433 will demonstrate. a considerably better durable CR when we have more data.

The N-803 + BCG CR rate of 71% at any time was achieved by retreating patients who normally would have been removed from the trial. By doing this they added another 16% to the CR rate. Without the retreatment their CR at any time would have been 55%.

You can listen to the interview with Dr. Karim Chamie at:

How Bladder Cancer Immunostimulant N-803 May Shake Things Up

For the transcript you need to do a free registration with Medscape. Here are some interesting quotes from it:

"Probably the most important thing that I've learned from this study is that the data look really promising. We had a 71% complete response, and the median durability is about 2 years. You say, "Okay, 2 years later, 35% of the patients are still disease-free, but that means that 65% of the patients either failed initially or failed ultimately." The lesson that we've learned from this is that only about 15% of patients went on to get a cystectomy. I think what we're learning is that maybe these patients' cancers are not as aggressive as we originally thought. The classic teaching during residency and fellowship is that in someone who has BCG-unresponsive bladder cancer — at least based on Harry Herr's study data — you've got to do that cystectomy because their outcomes are significantly better. What we're seeing is that at least in the KEYNOTE-057 study and in this study, most patients didn't have a cystectomy, and they're still alive and doing well. We're becoming a lot more comfortable in our own skin managing patients who failed some of these advanced options. So, I think that's the biggest lesson I've learned from this study."........................

...................."This is a single-arm study, but we did deviate in the sense that in most studies if a patient had a recurrence of bladder cancer, despite an induction course of a study drug, they were deemed ineligible to receive any additional drug. They basically were eliminated from the trial or excluded from pursuing additional treatment in the study. What we felt was that we were truly looking at patients with BCG-unresponsive disease, and these were patients who absolutely refused a cystectomy. So, we thought, "What if we actually allow patients who maybe had a partial response and see if we can keep them on the study and reinduce them?" Or if they've got low-grade disease, just keep them on the study and continue treatment as though they didn't have a recurrence. There were some modifications in patients who had carcinoma in situ (CIS). Maybe the CIS got a little smaller visibly, even though that's an artificial definition that we were allowed to pursue in the study.
 
What we found was that most of the complete responses occurred after the induction course. About 55% of patients who received an induction course had a complete response. But that meant that 45% of the people didn't, so they failed the study. What we did was give some of those patients a second shot of an induction course. We found we were able to get an additional 16% of patients to have a complete response. That's how we came up with 71%. We were able to get 55% plus 16%, and that got us to 71% of patients as complete responders."

Dr. Chamie also talked about the QUILT 2.005 study for BCG-naive patients which involves using N-803+BCG as a first line treatment and comparing with the use of BCG by itself. This trial has been put on hold because of the shortage of BCG.
Comment by ScienceFirst on Apr 20, 2023 1:18pm
Eoganacht ... Amazing perspectives.  Thanks for sharing the finding and transcript.
Comment by ScienceFirst on Apr 20, 2023 1:42pm
A Jan. 10 2023 article on ImmunityBio ... Some interesting insights and numbers in yellow ...     ImmunityBio (IBRX) Stock: Relief For Bladder Cancer Not Assured   The standard of care for non-muscle invasive bladder cancer (NMIBC) following unsuccessful therapy with Merck’s (MRK) Bacillus Calmette-Gurin (“BCG”) is surgery, namely cystectomy. In patients who are unfit ...more  
Comment by ScienceFirst on Apr 20, 2023 1:58pm
With Eoganacht's new interview where InmunityBio mentions that they initially had a CR of 55%, before retreating, this means we already equal them, even with our latest data that contains 12 undertreated patients out of 25 patients (so 48% of our pool of patients),  where we got 53% of CR. With only 2 treatments over the many for the N-803+BCG(see below), and not having to rely on BCG, ...more  
Comment by DJDawg on Apr 20, 2023 1:45pm
Interesting find! I'm confused about the protocol. "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 ...more  
Comment by ScienceFirst on Apr 20, 2023 2:02pm
DJDawg ... You have the proper reading.
Comment by Eoganacht on Apr 20, 2023 2:05pm
Yes that makes sense. It seems that 29% of patients didn't respond, 55% did respond and 16% more  responded if you kept treating them after recurrence. When you hit 24 months 35% of patients still had a CR, but who knows how long that CR would last without additonal treatments.
Comment by ScienceFirst on Apr 20, 2023 2:17pm
Exact Eoganacht.  ImmunityBio is doing the same thing they did we BCG. Repeating over and over the treatment, over a very long period of time.  Our Ph. 1B confirmed that, when we saw how many times our 6 ph. 1b patients had been treated with BCG (9, 11, 24, 24,12,18 times) prior to being declared BCG-Unresponsive and another chance with our treatment. Number of prior BCG instills https ...more  
Comment by DJDawg on Apr 20, 2023 2:28pm
I feel that this picture tells a better story. https://twitter.com/NEJMEvidence/status/1608100507368968194/photo/1 Note that the asco poster for TLD-1433 is similar format in some ways except for ASCO they included all the 3 month Non responders whereas the N-803 display just shows the 58 responder.
Comment by Eoganacht on Apr 20, 2023 2:40pm
Thanks for that. So 28 out of 82 patients were still CR at 24 months - 34%  7 of those 28 are no longer in the trial (for whatever reason) so they won't know how long they will maintain their CR. 21 CR patients - 26% - will continue being assessed and will presumably continue getting treatments as it is deemed appropriate.
Comment by ScienceFirst on Apr 20, 2023 3:23pm
DJDawg ... Nice observation regarding the sowing of only responders (n=58).
Comment by Eoganacht on Apr 20, 2023 3:58pm
From the chart DJDawg found we can see that not many of the 13 out of 82 patients (16%) who brought the CR at any time rate up from 55% to 71%, by being retreated after recurrence, benefited much from the exercise. 8 of the 13 eventually experienced high-grade recurrences and 1 was lost to follow up either through death or withdrawal from the trial for another reason. Only 4 of these ...more  
Comment by Rumpl3StiltSkin on Apr 20, 2023 4:13pm
Hmm, Yes I can see this also working against TLT in NMIBC. We are talking an older more fragile population that might have other health issues.
Comment by O12009 on Apr 21, 2023 8:19am
Great post. I was wondering Is this 24 months after their first treatment or 24 months after the last treatment. A very big difference. If it is after the first treatment, they may have only had their last treatment 30 days before 24 months was up. What was our % after 30 days?
Comment by Eoganacht on Apr 20, 2023 2:24pm
It's hard to keep track of how many treatments the patients that are CR at 2 years have had (maybe 24?) and how many they may yet have to get (9?). With Ruvidar it's 2 treatments period. It's far more convenient. It's cheaper. Safety is better. Durable complete response is very likely better. And there is no dependence on BCG, which is in short supply.
Comment by Rumpl3StiltSkin on Apr 20, 2023 2:50pm
Not gonna disagree Eoga, Though I also think that NMIBC dosimetry here is inprecise. So IF the treatment doesn't 'take' for some reason after 2? No reason to stop there...
Comment by Eoganacht on Apr 20, 2023 3:20pm
I wasn't suggesting that TLD1433 PDT should necessarily stop at 2 treatments. If there is a chance to benefit patients who have recurred after 2 treatments I don't see why they shouldn't try again. ImmunityBio got 16% more CRs by retreating, maybe this would also work for Theralase. And with Theralase there may be a better chance the CR would be durable.
Comment by Rumpl3StiltSkin on Apr 20, 2023 3:37pm
Right Eoga, I think TLT has a chance to prove that it can get the CRs % quite high IF they could keep on treating these NMIBC patients. Probably way more than the 16% improvement of this other study. Though with some future cancer indications TLT might not have that much % room for improving on the orig 2 treatments. :-)
Comment by N0taP00p on Apr 20, 2023 4:23pm
Eoganacht, I was curious about the assumption that Theralase can potentially continue treatments beyond the first two.  Wouldn't that fall outside the treatment protocol filed with the FDA for phase 2b?
Comment by Eoganacht on Apr 20, 2023 4:37pm
I don't think they could do it in the current trial. But maybe they could do it in the future given the demonstrated safety and tolerability of the treatment.
Comment by ScienceFirst on Apr 20, 2023 4:40pm
NP ... he was talking outside the current Ph. 2.   Kind of off-label.
Comment by Rumpl3StiltSkin on Apr 20, 2023 6:25pm
Yep Poop, I was just spit ballin'. Not part of our current Phase 2. Just trying to compare TLT potential vs that other company study.
Comment by CancerSlayer on Apr 20, 2023 10:07pm
  Off-label use is actually pretty common in the medical field, especially in oncology when existing approved therapies often fail individually to meet the demands of cancer patients.  This off-label approach is precisely what is currently being employed by many urologists/medical centers for the treatment of high-risk NMIBC (both pre BCG & post BCG treatment failure...& being ...more  
Comment by ScienceFirst on Apr 20, 2023 10:16pm
CancerSlayer ... Great and accurate posts.  And good link too.
Comment by BlueFranky on Apr 20, 2023 10:43pm
Slayer - I for one am grateful for your contribution to this board - thank you!
Comment by Rumpl3StiltSkin on Apr 20, 2023 2:19pm
IF, TLT is also allowed this leeway, to keep treating patients after recurrance, How large of a total CR% will they eventually get?  I think after 5-6 treatments the CR % data could get to the 90s... Though with less overall cost, way less toxicity, way fewer overall treatments... :-)
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The Road to Saving Lives: Clinical Study Underway

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