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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 Aug 28, 2023 7:44pm
195 Views
Post# 35609007

RE:Ph. 3 study ends early after 'dramatic' benefits

RE:Ph. 3 study ends early after 'dramatic' benefits

A repeat of Ph. 1B is also possible even in a pivotal Ph. 2 or Ph. 3.

Cabometyx Ph.3 study ends early after researchers see 'dramatic' benefits in neuroendocrine tumors, Exelixis says | Fierce Pharma

 

A bit like our Ph. 1b but for a pivotal Ph. 3 for an advanced pancreatic indication.
 
That would be interesting if the same would happen with our NMIBC Ph. 2.
 

Cabometyx Ph. 3 study ends early after researchers see 'dramatic' benefits in neuroendocrine tumors, Exelixis says

 

It's not always a good thing when a drug developer stops a cancer trial. But in a recent case for Exelixis, a Cabometyx trial ended early because of an undeniable efficacy showing.

 
 

In this study, the company’s Ipsen-partnered tyrosine kinase inhibitor Cabometyx (cabozantinib) was studied in patients with advanced pancreatic or extra-pancreatic neuroendocrine tumors who progressed after prior systemic therapy. In the phase 3 Cabinet trial, the drug showed a “dramatic improvement” compared with placebo in prolonging the time without disease progression or death, the company said.

The trial's Independent Data and Safety Monitoring Board (DSMB) unanimously recommended to unblind and end the study, allowing the patients on placebo to switch over to Cabometyx. Now, in the wake of that decision, Exelixis plans to discuss the results with the FDA.

“We are pleased to see that cabozantinib improved outcomes for two additional patient populations living with advanced, difficult-to-treat cancers,” the company’s senior vice president of medical affairs, Will Berg, M.D., said in a statement.

Analysts with William Blair were “pleasantly surprised” by the win, the team wrote to clients. An FDA review in this disease setting will likely take about a year, the team said.


https://www.fiercepharma.com/pharma/exelixis-cabometyx-trial-wraps-early-after-proving-dramatic-improvement-pancreatic-tumors
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