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therefore INCREASING THE STRICK PRICE
WARRANTS TRADE IN OPEN MARKET
Their burn rate is slow they are good for about a year.
LAST NINE MONTH BUR N RATE WAS .375mil PER QUARTER!
Interesting company but a few concerns, quote:
For the nine-month period ended September 30, 2021, the Company had a net loss of $ 3,129,731 (2020 -
$4,715,771), an accumulated deficit of $51,810,968 (December 31, 2020 - $48,506,467) and has historically
used net cash in operations. These conditions indicate the existence of material uncertainties that casts
substantial doubt about the Company’s ability to continue as a going concern. The Company's ability t o
continue as a going concern is dependent upon achieving a profitable level of operations and obtaining
additional financing, neither of which is assured. The Company has been able to raise capital to continue to
market its products and continues to develop sales opportunities that could result in additional sales of its
products in the future. These condensed interim consolidated financial statements do not give effect to any adjustments which may be necessary should the Company be unable to continue as a going concern and be
required to realize its assets and discharge its liabilities in other than the normal course of business and at
amounts different from those reflected in the accompanying condensed interim consolidated financial
statements. These adjustments could be material.
The Company’s objective is to maintain a sufficient capital base to support future research, development and
strategic business initiatives allowing the Company to invest in its future and maintain investor, creditor and
market confidence. Sales of the TLC-2000, the Company’s existing product line have not met expectations and
have not been sufficient in and of themselves to enable the Company to fund all its continuing development
and commercialization efforts and, accordingly, management is pursuing alternate financing sources to fund
the Company’s development and commercialization efforts. The Company has successfully raised capital
through equity offerings in 2019 however, there is no guarantee that the Company will be able to raise
additional capital on terms and conditions agreeable to the Company.
https://theralase.com/wp-content/uploads/2021/11/Q321-Financial-Statements-Final-3.pdf
That doesn't sound to good to me, not much cash left and sales of TLC-2000 not going well.
I am thinking about buying a small position but above statements worries me.
I guess the bladder cancer laser treatment is the hope for this company for survival and big earnings.
$TLTFF 07 .14 .28 .35 What's next in your pattern?
$TLTFF
12OCT20 TO PRESENT .076-.3775
$IBRX
12OCT20 TO PRESENT 8.38 - 6.18
$SESN
12OCT20 TO PRESENT 1.09 - .5811 .
07 .14 .28 .35 What's next in your pattern?
$TLTFF Consolidating into uptrend! The best CR rates!!!
And the FDA know it. that's why the BTD and AA are in play now.
They are not making pot brownies here.
When in doubt zoom out..
Look to the big picture.
Solid science solid results
No smoke and mirror numbers.
That was just steady all day accumulation.
Perhaps the market wants 2b having this stock? TLTFF
Who's PIVOTAL PH2B NMIBC NONRESPONSE FDA DARLING?!?!?!?!?!
Almost like the FDA was saying 2b or not 2b...
call me call me anytime call me..
No new patient updates since nov 29 2021.
I do tricks for chili dogs..
After 3 I roll over and play dead...
Some excitement happening today. Is it indigestion or the feeling that the story is too good to be true?
Puppies love chillidogs!
When Theral-ACES HIGH hits the next gears..
We hear about it after they have talked with the FDA.. YES???
Go check it out .... maybe im wrong?? naw... i don't think so....
vroom vroom...
TLTFF LONG AND STRONG ON SOLID SCIENCE!!!
If Theralase has toppling data current/material news. The may take that data to date to the FDA. Sometime Theralase cannot report due to regulatory restrictions.
Competitors will know this and report during the assessment period trying to inspire impatience.
Here is why I am considering this scenario...
They normally report
Cancer research updates and Cutting edge covid research updates in the quarterly.
However this time around they have PR the covid research
Theralase® Demonstrates Proof-of-Concept for Canadian-Made COVID-19 Vaccine
Toronto, Ontario – February 7, 2022
Ok then look to the insider buying...
The Corporate presentation is of no interest to the FDA.
The Company newsletter is of no interest to the FDA.
The FDA is interested in the data to date.
May 19, 2020Shawn Shirazi went on to say, "In a 3Q2019 conference call with the FDA, it was discussed and agreed between the FDA and the Company,
post receipt of the FDA IND authorization, based on the clinical study data collected to date.
It was further discussed and agreed that Theralase would potentially be eligible for Breakthrough Therapy Designation ("BTD") and/or Accelerated Approval (AA)
if Theralase can demonstrate clinically significant results (high safety profile and high efficacy response), similar to the safety and efficacy results observed in the Phase Ib NMIBC study (high safety profile and 67% CR) at an interim analysis of approximately 20 to 25 patients enrolled and successfully treated."
This is the link to the quarterly newsletters... Currently the public only has information on this study up to NOV 28 2021.
Link to TLTFF NEWSLETTERS
TLTFF long.
Interesting Science for sure..
The company website shows the depth of research going into TLD-1433.
https://theralase.com/anti-cancer-therapy/research-publications/
GLTA
$TLTFF Darling... CAN WE JUST TALK??.. CAN WE JUST TALK??
THINK ABOUT WHERE XRAY IS GOING??
Theralase® Granted United States Patent to Destroy Cancer Cells with X-Ray Activated Photo Dynamic Compounds March 4, 2019
I just found it interesting back when they released the above release that they included bladder cancer.
Back in the day they were publishing info on solid tumor work.
New lab and they are getting things done for sure!
Did ya'll see that fund mangers face when they were asking Shawn if lil ol therylase could get to standard of care for NMIBC...hahhahhhha golden moment...hhshshshshshs
Shawn stonewalled them alll....hahahhahahaha
Cool a$$ a freakin ice cube baby.... hahahahha
Shawn knows....
Hey... check into patient 4 from study one.. yeah dig into that about the rules the FDA had to change/clarify/set up for this study. Yeah Theralse almost hit 100 percent there...
Bullish baby bullish... Let's go!
TLTFF the science is strong in this one!
Look to the cost expense/number of treatments for alternatives. BCG is in short supplly. A treatment like that using scare resources will always be expensive.
.
Alternative treatments are very cost prohibative
and will have a very very very difficult time competing with Theralase.
JMO Time for a coffee.
While others are giving their numbers a nice massage.
Theralase dialed things back on this freakin beast for cation then after they let the kids drive the care with dad well they are ready to drive it for themselfs..... YES Baby YES.....
Full doses and full throttle!!
TLTFF for NMIBC NONRESPONSE!!
FEB 7 COPR PREZ BASED OFF NOV 29 2021 DATA
Latest Coprate presentation FEB 7 2022 based of NOV 29 2021 data.
30 patients treated to date in the Phase II NMIBC clinical study
3 patients treated in the
Phase Ib NMIBC clinical
study
Total population of 33
patients patietheralase.com/wp-content/up...nts 5 clinical study sites open in Canada and 7 in United States
Feb 7 2022 copr prez 33 total patients treated (3 from phase one) NO NEW REPORTING FROM 29 NOV 2021!!!
https://theralase.com/wp-content/uploads/2022/02/Corporate-PPT-020722.pdf
Note 32 Theralase® Press Release - Theralase Releases 3Q21 Financial Statements and Newsletter – November 29, 2021 32 Theralase® Press Release -
From the last quarterly newsletter. 3Q2021 | NOVEMBER 2021
Study II Status:
Theralase® has enrolled and treated 30 patients in a Phase II Non-Muscle Invasive Bladder Cancer ("NMIBC") Clinical Study ("Study II") (including three patients from the Phase Ib NMIBC clinical study (“Study”) treated at the Therapeutic Dose) for a total of 33 patients.
last quarterly newsletter
https://theralase.com/wp-content/uploads/2021/11/3Q-2021-Newsletter.pdf
July 30, 2020, Of the 4 patients that were removed from Study II, the clinical protocol in effect at the time stated in the patient withdrawal criteria that “Patients found to have at Day 90 new T1 high-grade disease, with or without CIS” and “Patients found to have unchanged or worsening CIS at 3 months” will be removed from Study II.
Of the 4 patients removed from the Study, they presented with “unchanged CIS at 3 months”.
This was an oversight on behalf of the Company and the clinical protocol has since been updated to remove these two specific patient withdrawal criteria, maintaining the key patient withdrawal criteria of NMIBC progression,
______________________________________
Looks like 8 of the First 12 from phase 2 are up for the 2nd treatment at full dose!
67% CR @ 18 months. Patients removed after 24 moths from the study.
Only the doc knows about the 24 mo results from the phase 2 but.... but he diald back the first dozen to lower dose levels....
Before 409 was on the market it was 410 but it was so strong they had to dial it back. just sayin.
TLTFF GOLD STANDARD FOR NMIBC NONRESPONSE
___________________________________________
Looks like 8 of the First 12 from phase 2 are up for the 2nd treatment at full dose!
67% CR @ 18 months. Patients removed after 24 moths from the study.
Only the doc knows about the 24 mo results from the phase 2 but.... but he diald back the first dozen to lower dose levels....
Before 409 was on the market it was 410 but it was so strong they had to dial it back. just sayin.
TLTFF GOLD STANDARD FOR NMIBC NONRESPONSE
________________________________________________
Picked up more Good CR from 1 of 2.
12 -4=8-2=6 patients to get second dose full.
maybe we get 3 of 6 back from our first dozen. yep yep
Note: There are 2 patients that received an unoptimized primary Study II Treatment and were diagnosed as non-responsive; however, they then received an optimized maintenance Study II Treatment. Analyzing these 2 patients, 1 remained non-responsive and 1 achieved a CR at 270 days and PR at 360 and 450 days, respectively.
As of November 29, 2021
BTD Dr Vera is probably expecting news soon and a continued date change of the BTD as based on the most currently data in 2022 not 2021.
Its really a whole new year now. And i think its gonna be a good one.
1/28/2020 Roger John Dumoulin-White Director Buy 34,000 C$0.30 C$10,030.00 6,686,687
https://www.marketbeat.com/stocks/CVE/TLT/insider-trades/Theralase insider buying
They can't buy in face of material news.
Did he buy in jan of last year.
Speculation... news is about to drop.
They are trying to rattle with data from 29 nov 2021
I'm on the floor rolling.
of course new data will be rollin in 2022!!
$TLTFF
The time line of 2022 for BTD is currently based off data backlocking from NOV 29 2021.
And that latest corprate prezzy is based off that data.
Shall the market expect new data may affect the timetable?
Well yes, it already has.. Look at the timetable in the corp prezzy the quarter back.
Yep that copr prezzy date is moving closer to us with the new data releases.
And of course that data is only up till nov 29 2021.
We will get some data updaates in 2022 also.
Yep prolly more data and no quarterly newsletters anymore.
Hell i dont' know im just a hick doin oil changes... LOL
Keep up the good work ..123414
Who know why stocks fluctuate so... me thinks there is a a big shake going on.. Besides the stock was up big over the last month..
TLTFF is seeking a firm stepping up point.
Phase II news will be the answer...
Why are we down nearly 10% on volume?
$TLTFF XRAY ATIVATION AND A NEW LAB.
About NMIBC
In 2016, an estimated 79,030 adults (60,490 men and 18,540 women) were diagnosed with bladder cancer in the United States. Among men, bladder cancer is the fourth most common cancer. It is estimated that 16,870 deaths (12,240 men and 4,630 women) from this disease will occur in 2016. Among men, bladder cancer is eighth most common cause of cancer death.
About GBM
There are an estimated 24,000 new cases of malignant gliomas diagnosed in the US annually, with more than 14,000 deaths. In the majority of cases, they recur following initial treatment, especially for GBM, the most common and lethal form of brain cancer. Most patients do not survive beyond 2 years, post diagnosis.
About NSCLC
Lung cancer is by far the leading cause of cancer death among both men and women. Out of all types of lung cancer, NSCLC accounts for 80 to 85% of cases. The American Cancer Society's estimates for lung cancer in the United States for 2018 are:
· About 234,030 new cases of lung cancer (121,680 in men and 112,350 in women)
· About 154,050 deaths from lung cancer (83,550 in men and 70,500 in women)
About Theralase® Technologies Inc.
https://www.accesswire.com/537731/Theralase-Granted-United-States-Patent-to-Destroy-Cancer-Cells-with-X-Ray-Activated-Photo-Dynamic-Compounds
$TLTFF The Gold Standard for NMIBC NON-RESPONSE!!
The science is solid.
Who's First in Class?? Little ol TLTFF?
Who ran from .37 to SIX DOLLARS A SHARE?? SESN TILL THE FDA BACKBURNER!
With SESN safety violations the FDA told them to sit in the corner. (DONW DONW DONW DOWN DA DOOBY DOWN DOWN DOWN DOWN DOWN.... OWCH OWOCH OWWWWOCH OWWWWOWO OCUCH...
You bad boy!!
SESN WAS FIRST IN CLASS BUT THAT CAR BLEW A ROD IN THE RACE
sesn has to push it back to the shop and pull the engine!!
The engine of their NMIBC NON-RESPONSE HAS BLOWN.
Their major catalyst has failed.
So do we have a new first in class new reporter guys??
Who is going to get scooped in the news world???
Yeah.. Who will be the last to know?
When that sesn engine was blowing black smoke those lubby pros knew what to look for.
Them special mechanic were like "Dang boys that aint good ... the engine is gonna blow!!
The average popcorn eating sports fan is so happy to eat popcorn they dont care about engine??
Guys and Galls sports fans of all ages Lets post the question.
Who is First in Class for NMIBC-NONRESPONSE??
Whos on Full Throttle in race for NMIBC-NORESPONSE??
$TLTFF Demonstrates Proof-of-Concept COVID-19 Vaccine
Theralase® Demonstrates Proof-of-Concept for Canadian-Made COVID-19 Vaccine
Toronto, Ontario – February 7, 2022, Theralase® Technologies Inc. (“Theralase®” or the “Company”) (TSXV: TLT) (OTCQB: TLTFF), a clinical stage pharmaceutical company focused on the research and development of light activated Photo Dynamic Compounds1 (“PDC”) and their associated drug formulations intended for the safe and effective destruction of various cancers, bacteria and viruses, has demonstrated proof-of-concept for the development of a Canadian-made SARS-CoV-2 (“COVID-19”) vaccine.
In August 2020, Theralase® reported that it had executed a Sponsored Research Agreement (“SRA”) with the University of Manitoba (“UM”) medical microbiology department to commence research and development of a Canadian-made vaccine, utilizing Theralase®’s patented and proprietary PDC, TLD-1433.
In November 2020, Theralase® reported that, UM was able to demonstrate that TLD-1433 was effective in the rapid destruction of various viruses, including: H1N1 Influenza, Zika and a Biological Safety Level (“BSL”)-2 coronavirus at low nanomolar (“nM”) concentrations.
All these enveloped viruses are similar in structure to SARS-CoV-2 virus (BSL-3), which is responsible for COVID-19. These initial results strongly suggested that Theralase®’s PDC technology may be used to develop an inactivated virus vaccine2 that may be effective against COVID-19 and hence warranted further preclinical evaluation.
Further research by UM also identified that the spike protein responsible for the transmission of a coronavirus into a host cell, remained intact after light-activated TLD-1433 inactivation, suggesting that the vaccine developed by this technology could potentially stimulate a protective antibody immune response in a mammalian host.
In April 2021, Theralase® reported that it had executed a Collaborative Research Agreement (“CRA”) with the Public Health Agency of Canada’s (“PHAC”) National Microbiology Laboratory to further expand upon the research and development achieved at UM, by researching and developing a Canadian-based COVID-19 vaccine.
Under the terms of the agreement, Theralase® and PHAC are collaborating on the research, development and optimization of a COVID-19 vaccine by inactivating the SARS-CoV-2 virus with Theralase®’s light-activated PDC, TLD-1433.
Theralase® is pleased to be able to report today that PHAC has demonstrated that light-activated TLD-1433, was effective in rapidly inactivating the SARS-CoV-2 virus by up to 99.99%, compared to control in an in vitro study. Further research is required to confirm these findings.
These results have now laid the groundwork for the next phase of the CRA, which is evaluating the Theralase® COVID-19 vaccine in the ability to prevent animals from contracting COVID-19, when exposed to the virus.
Darwyn Kobasa, Ph.D., Head, High Containment Respiratory Virus Group, Special Pathogens, PHAC, stated “My team’s initial results indicate that, when activated by light, TLD-1433 is very effective in inactivating the COVID-19 virus at low concentrations, thus demonstrating proof-of-concept in the development of a Canadian-made COVID-19 vaccine.”
Kevin Coombs, Ph.D., Professor, Department of Medical Microbiology at UM, stated, “The work conducted at my lab and the work conducted by PHAC’s National Microbiology Laboratory, has demonstrated that a large range of enveloped viruses can be successfully inactivated by light-activated TLD-1433 at low concentrations. I am delighted that Theralase®’s and my initial preclinical research has proven to be effective in COVID-19.
Dr. Arkady Mandel, M.D., Ph.D., D.Sc., Interim Chief Executive Officer and Chief Scientific Officer, Theralase® stated, “The latest preliminary results by Dr. Kobasa and Dr. Coombs, demonstrates that the Theralase® vaccine may potentially be effective as a Canadian-made wholly-inactivated vaccine to prevent individuals from contracting COVID-19 in the future and warrants further research to confirm the findings. The research also demonstrates that the Theralase® platform is extremely versatile, with an ability to be applicable to a wide range of enveloped viruses. This would allow the Company to tailor the vaccine to be potentially effective against contracting various viruses (existing and/or new) and their associated variants. Based on this encouraging data, the Company intends to move forward in the research, development and commercialization of the Theralase® COVID-19 vaccine, subject to the required regulatory approval.”
PDCs are Light sensitive compounds that when activated by light at a particular wavelength can produce reactive oxygen species that can cause inactivation of cells or viruses through oxidative stress.
The Company does not claim or profess that they have the ability to treat, cure or prevent the contraction of the COVID-19 coronavirus.
About TLD-1433
TLD-1433 is a patented PDC with over 10 years of published peer reviewed preclinical research and is currently under investigation in a Phase II Non-Muscle Invasive Bladder Cancer (“NMIBC”) clinical study for Bacillus Calmette-Gurin (“BCG”)-Unresponsive patients at 5 Canadian Clinical Study Sites (“CSS”) and 7 US-based CSS.
Theralase® Demonstrates Proof-of-Concept for Canadian-Made COVID-19 Vaccine – Theralase Technologies
https://theralase.com/theralase-demonstrates-proof-of-concept-for-canadian-made-covid-19-vaccine/
LINK TO OTHER NEWS
https://theralase.com/press-releases/
$TLTFF Theralase -Collaborative Research with PHAC
April 9, 2021, Theralase® Technologies Inc. (“Theralase” or the “Company”) (TSXV: TLT) (OTCQB: TLTFF), a clinical stage pharmaceutical company focused on the research and development of light activated Photo Dynamic Compounds (“PDC”) and their associated drug formulations to safely and effectively destroy various cancers, bacteria and viruses, announced today that it has executed a Collaborative Research Agreement (“CRA”) with the National Microbiology Laboratory, Public Health Agency of Canada (“PHAC”) for the research and development of a Canadian-based SARS-CoV-2 (“COVID-19”) vaccine.
Under the terms of the agreement, Theralase® and PHAC are collaborating on the development and optimization of a COVID-19 vaccine by treating the SARS-CoV-2 virus grown on cell lines with Theralase®’s patented PDC and then light activating it with Theralase®’s proprietary TLC-3000A light technology to inactivate the virus and create the fundamental building blocks of a COVID-19 vaccine. This inactivated virus would then be purified and used to inoculate naive animals followed by challenge with the SARS-CoV-2 virus, to ascertain the efficacy of the vaccine. The project is entitled, “Photo Dynamic Compound Inactivation of SARS-CoV-2 Vaccine” and is expected to commence in mid-April 2021.
PHAC is a world leader in vaccine creation and has a long history of vaccine development. PHAC scientists developed the world’s first approved Ebola vaccine (Ervebo), which the Government of Canada donated to the World Health Organization (“WHO”) during the height of the 2014-16 Ebola outbreak and in the process helped to save countless lives in Africa.
Darwyn Kobasa, Ph.D., Head, High Containment Respiratory Virus Group, Special Pathogens, PHAC/NML, stated “Our research expertise will help assist Theralase® to research and develop an effective COVID-19 vaccine that is robust enough to vaccinate against the main phenotype of the disease and its emerging variants. NML has unique capacity to conduct preclinical research in animal models, that must occur in high containment laboratory space, which is essential to the development of an effective COVID-19 vaccine. I am delighted for having the opportunity of testing the Theralase® anti-viral platform technology at PHAC. The in-vitro data I have reviewed demonstrates that Theralase®’s PDCs have a very high log kill of various Biological Safety Laboratory (“BSL”)-2 viruses at nanomolar concentrations. The focus of our CRA is to demonstrate these same results using the SARS-CoV-2 virus, which is a BSL-3 virus. The tested efficacy in BSL-2 virus destruction, reported by Dr. Kevin Coombs of the University of Manitoba, shows that the Theralase® PDC is comparable to, or better than, many other anti-virals that my lab has tested. I look forward to working with Dr. Arkady Mandel and the Theralase® team in the development of this exciting technology.”
Dr. Kevin Coombs, Ph.D., Professor, Department of Medical Microbiology at University Manitoba, stated, “I am delighted to see that Theralase®’s and my initial in-vitro research into BSL-2 virus inactivation has successfully advanced to the next stage of evaluation against BSL-3 viruses and if proven successful, on to preclinical vaccine manufacture and vaccination of animals against the SARS-CoV-2 virus in a challenge model at PHAC.”
Dr. Arkady Mandel, M.D., Ph.D., D.Sc., Chief Scientific Officer, Theralase® stated, “In line with ongoing global efforts to combat the pandemic, the Company continues to move forward with the development of a safe and effective vaccine to inoculate individuals against COVID-19 and its variants. This new CRA enables Theralase the ability to collaborate with esteemed scientists at PHAC, who have the same mandate of developing new and improved vaccines for COVID-19 and its variants. This research and development will provide new opportunities for the Company; specifically, in the development of new anti-viral vaccination solutions, contributing to our growing platform of PDC-based technology applications. If proven successful, the Theralase® COVID-19 vaccine will support our healthcare professionals in safely and effectively combatting any new viral outbreaks, such as the one recently witnessed, with the global spread of COVID-19”.
The Company does not claim or profess that they have the ability to treat, cure or prevent the contraction of the COVID-19 coronavirus.
About Theralase® Technologies Inc.
Theralase® is a clinical stage pharmaceutical company dedicated to the research and development of light activated Photo Dynamic Compounds and their associated drug formulations intended to safely and effectively destroy various cancers, bacteria and viruses.
Theralase Commences Collaborative Research with National Microbiology Laboratory for Development of Coronavirus Vaccine – Theralase Technologies
$TLTFF MONTHEY CHART FROM MARCH2019-PRESENT.
The time period shows market confidence collapse and rebuild. After the stellar results from ph1. The company had to change gears. They pushed the clutch in changed gears and are now back on the throttle for the NMIBC NONRESPONSE RACE!!
Who is leading the pack?? Investors in the know go with the strongest!
It's a chart of beautiful symmetry.
With solid science and systematic progress for support.
The support for the company and
for the unmet medical need is very strong.
TLFFF FULL THROTTLE ON THE NMIBC NONRESPONSE.
TLTFF FULL THROTTLE ON CUTTING EDGE COVID RESEARCH.
$TLTFF THE BRIGHTTESTED LIGHT ON THE DARKEST NIGHT!
TLTFF Millions in the back and a tiny tiny tiny burnrate.
The SESN COMPETITOR FDA BACKBURNER WAS THE BURNER.
.37 TO SEX BUCKS. SESN WAS NOT THE STRONGEST.
SESN - got hit by the backburner. All those safety violations...
Go sit in the corner you bad boy!
TLTFF 67% CR @ 18 MONTHS PHASE1 FROM ONE TREATMENT
With patients released from the study at 18 months.
Only the doctor and the patient know the 24 month results.
But then the PI set the dosage back for the PH2 PIVITOL
at about a 70 percent dose for some of the for some of the first 12 patients treated in PH2 PIVITOL. Ph2 PIVITOL HAS TWO TREATMENTS. lol
What's up Doc?? Maybe you were concerned for overtreating patients and gave them the full dose on the next 6 month treatment as a mop up?
$TLTFF The market is aware of you!!
Here in the U.S.! In Canada maybe all of 6.618.
$TLTFF Forces are getting stronger and more bullish.
$TLTFF Fancy like Applebees on date night$$!!.
NMIBC NONRESPONSE FIRST IN CLASS
Theralase® Demonstrates Proof-of-Concept for Canadian-Made COVID-19 Vaccine February 7, 2022
The three month chart showS current market expectations.
SESN run from .37 to over 6 DOLLARS US
SESN BACKBURER FROM THE FDA ON THEIR NMIBC STUDY WAS THE BURNER.
jmo
TLTFF The data and science and time appear to be in strong favor of
$TLTFF
TLTFF Long
Down for the day sounds funny.
Letting a little steam off makes sense. And the price is down.
Share price is down 6/10,000 of a penny... or .0006 cents.
No one is letting go after the Covid news and looming Phase II updates. The only people buying are people who either stumble onto Theralase or investors who know people who talk about their research.
That makes about 1.103 people.. just a guess.
MM's are working to make sure there is no further gains to be added from yesterday's volume. They just wait for some of the air to go out of the balloon, and then start throwing out low volume trades to curb the sp appreciation. As long as "someone" is willing to sell below the Ask, at a ridiculously low share prices, then only higher volumes/demand can absorb those trades/shares and move up the sp. Just like yesterday.
It's the volume and demand for shares that requires the MM's to get out of the way of the Ask. Like yesterday. Meaning - they understood yesterdays volume and accumulation. So they didn't throw (much) lower priced shares out to curb the sp appreciation, or they would have been run over with no suppressed sp effect. IMO.
It's all psychological trading. The sky's not falling, and the trend and momentum has been established with the recent company progress.
Soon there will be even more eyes viewing this company's progress and attract more purchases and higher volume.
MM's and shorters are trying to do the same on the Canadian exchange.
A cure/therapy for cancer for $.35-$.50 a share? It's all about the DD and details.
Good luck to all. Regards,BK.
$TLTFF Demonstrates Proof-of-Concept for Canadian-Made COVID-19 Vaccine
Toronto, Ontario – February 7, 2022, Theralase® Technologies Inc. (“Theralase®” or the “Company”) (TSXV: TLT) (OTCQB: TLTFF), a clinical stage pharmaceutical company focused on the research and development of light activated Photo Dynamic Compounds1 (“PDC”) and their associated drug formulations intended for the safe and effective destruction of various cancers, bacteria and viruses, has demonstrated proof-of-concept for the development of a Canadian-made SARS-CoV-2 (“COVID-19”) vaccine.
In August 2020, Theralase® reported that it had executed a Sponsored Research Agreement (“SRA”) with the University of Manitoba (“UM”) medical microbiology department to commence research and development of a Canadian-made vaccine, utilizing Theralase®’s patented and proprietary PDC, TLD-1433.
In November 2020, Theralase® reported that, UM was able to demonstrate that TLD-1433 was effective in the rapid destruction of various viruses, including: H1N1 Influenza, Zika and a Biological Safety Level (“BSL”)-2 coronavirus at low nanomolar (“nM”) concentrations.
All these enveloped viruses are similar in structure to SARS-CoV-2 virus (BSL-3), which is responsible for COVID-19. These initial results strongly suggested that Theralase®’s PDC technology may be used to develop an inactivated virus vaccine2 that may be effective against COVID-19 and hence warranted further preclinical evaluation.
Further research by UM also identified that the spike protein responsible for the transmission of a coronavirus into a host cell, remained intact after light-activated TLD-1433 inactivation, suggesting that the vaccine developed by this technology could potentially stimulate a protective antibody immune response in a mammalian host.
In April 2021, Theralase® reported that it had executed a Collaborative Research Agreement (“CRA”) with the Public Health Agency of Canada’s (“PHAC”) National Microbiology Laboratory to further expand upon the research and development achieved at UM, by researching and developing a Canadian-based COVID-19 vaccine.
Under the terms of the agreement, Theralase® and PHAC are collaborating on the research, development and optimization of a COVID-19 vaccine by inactivating the SARS-CoV-2 virus with Theralase®’s light-activated PDC, TLD-1433.
Theralase® is pleased to be able to report today that PHAC has demonstrated that light-activated TLD-1433, was effective in rapidly inactivating the SARS-CoV-2 virus by up to 99.99%, compared to control in an in vitro study. Further research is required to confirm these findings.
These results have now laid the groundwork for the next phase of the CRA, which is evaluating the Theralase® COVID-19 vaccine in the ability to prevent animals from contracting COVID-19, when exposed to the virus.
Darwyn Kobasa, Ph.D., Head, High Containment Respiratory Virus Group, Special Pathogens, PHAC, stated “My team’s initial results indicate that, when activated by light, TLD-1433 is very effective in inactivating the COVID-19 virus at low concentrations, thus demonstrating proof-of-concept in the development of a Canadian-made COVID-19 vaccine.”
Kevin Coombs, Ph.D., Professor, Department of Medical Microbiology at UM, stated, “The work conducted at my lab and the work conducted by PHAC’s National Microbiology Laboratory, has demonstrated that a large range of enveloped viruses can be successfully inactivated by light-activated TLD-1433 at low concentrations. I am delighted that Theralase®’s and my initial preclinical research has proven to be effective in COVID-19.
Dr. Arkady Mandel, M.D., Ph.D., D.Sc., Interim Chief Executive Officer and Chief Scientific Officer, Theralase® stated, “The latest preliminary results by Dr. Kobasa and Dr. Coombs, demonstrates that the Theralase® vaccine may potentially be effective as a Canadian-made wholly-inactivated vaccine to prevent individuals from contracting COVID-19 in the future and warrants further research to confirm the findings. The research also demonstrates that the Theralase® platform is extremely versatile, with an ability to be applicable to a wide range of enveloped viruses. This would allow the Company to tailor the vaccine to be potentially effective against contracting various viruses (existing and/or new) and their associated variants. Based on this encouraging data, the Company intends to move forward in the research, development and commercialization of the Theralase® COVID-19 vaccine, subject to the required regulatory approval.”
PDCs are Light sensitive compounds that when activated by light at a particular wavelength can produce reactive oxygen species that can cause inactivation of cells or viruses through oxidative stress.
The Company does not claim or profess that they have the ability to treat, cure or prevent the contraction of the COVID-19 coronavirus.
About TLD-1433
TLD-1433 is a patented PDC with over 10 years of published peer reviewed preclinical research and is currently under investigation in a Phase II Non-Muscle Invasive Bladder Cancer (“NMIBC”) clinical study for Bacillus Calmette-Gurin (“BCG”)-Unresponsive patients at 5 Canadian Clinical Study Sites (“CSS”) and 7 US-based CSS.
About Theralase® Technologies Inc.
Theralase® is a clinical stage pharmaceutical company dedicated to the research and development of innovative Anti-Cancer Therapy (“ACT”) technologies intended to safely and effectively destroy various cancers, bacteria and viruses, while preserving patient Quality of Life (“QOL”).
https://theralase.com/theralase-demonstrates-proof-of-concept-for-canadian-made-covid-19-vaccine/
if ya feel like digging through old PR you will find they already have preliminary research on several other cancers
.https://theralase.com/press-releases/
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They have their own lab now and are really going at it...
It is good to do DD on this company.
$TLTFF 67% CR ON ONE TREATMENT FULL DOSE
Little Duece Coup
The little deuce coup of NMIBC non response.
$TLTFF Continues to validate the science and processes.
GOLD STANDARD FOR NMIBC NONRESPONCE.
$TLTFF The market is seeing the value. Validation continues
$TLTFF Covid research progressing nicely. Agreements with the Canadian Government.
Covid News was unexpected..
Good Bladder Cancer news and we will be trading over a dollar.
Just guessing.
That news is expected soon according to 123414..
California here I come..
You and the two or three others of us! Unbelievable.
The news explains the pps rising...
Glad to be watching the story unfold.
$TLTFF Nice progress guys!! With ORF and the Canadian Gov backing the play we are on our way. Millions in the bank and a tiny tiny tiny burnrate because they have so much support.
Good Job on the Covid research guys. We know you will keep up the good work!!
They were excited for NMIBC at SESN First in class? NOT!!!
The Company was looking at a major catalyst in 2021, the approval of Vicineum, a potential best-in-class therapeutic for the treatment of non-muscle invasive bladder cancer (NMIBC) in the U.S. Sesen has submitted the MAA for Vicineum to the EMA in March 2021, and anticipates an EU approval in 2022. aviseanalytics.com/4-biotec...