Post by
gonefishing2022 on Aug 12, 2024 7:56pm
SO IM MISSING THE GOOD NEWS
Can Anyone explain what this exciting news is and the share price goes down and I don't have pie in the sky evaluation. I don't see this going 2 dollars anytime soon. Also I don't really see a change until 2026..
Go Tell Me I'm wrong
Comment by
Beano349 on Aug 12, 2024 8:10pm
The good news was the new 450 CR tracking of over 40%. 1 treatment, and a CR over 40 over 1 year later. That's a big deal, but we still need approval...
Comment by
Oden6570 on Aug 13, 2024 7:02am
As well only 1 or 2 treatments as an outpatient
Comment by
Lesalpes29 on Aug 13, 2024 7:31am
Good results (we have already) + money for at least one year and I will be on the buy side. GL
Comment by
menoalittle on Aug 13, 2024 5:00pm
After all... look at the stats for colon cancer: Colorectal cancer is the third most common cancer worldwide, accounting for approximately 10% of all cancer cases and is the second leading cause of cancer-related deaths worldwide
Comment by
DJDawg on Aug 13, 2024 10:13pm
This would require IV therapy with rutherrin which is a different compount. So ruvidar, approved, can't jump from bladder med to IV med. Good thought. The big plan would be to show efficacy at gbm and nsclc and then at that point you could tally up approvals for just about any cancer that likes iron (they all do, especially solid ones).
Comment by
bigkagan on Aug 13, 2024 10:18pm
I wonder if somebody from the company got cancer would he use rutherrin with x-rays on himself even without any permits
Comment by
Tarbaby on Aug 14, 2024 10:09am
Very good point...using xray pdt. That is likely the most valuable asset TLT.v has. Its a sleeping giant that should be out there curing cancer. If I had incurable cancer I would try using other pdt compounds combined with xrays. There are a few such compounds I believe.
Comment by
Eoganacht on Aug 14, 2024 9:27pm
I have a hunch we're going to see the DOR format from now on. It"s the way all of our competition presents their data. Maybe this was a suggestion from the biostatistics organization which is helping with the BTD application.
Comment by
Donein25 on Aug 15, 2024 7:48am
From what you are saying; it sounds like in approximately 9 months time we will have about 60 folks evaluable at 2 years?
Comment by
Donein25 on Aug 15, 2024 10:32am
I see where you are going with this Dawg. It sort of ties in to what I said earlier about the significance of "75 patients". Roger stated this week that we have already met all 3 endpoints. So the 2 year data and 75 patients really is not about BTD, its beyond that. (Immuno got BTD in 2019 just by hitting its first endpoint)
Comment by
Lesalpes29 on Aug 15, 2024 7:56am
The act is safe, with good or very good results. FDA will give us pre-BTD and BTD this year (it's my bet). The real 2024 Christmas gift could be AA, we can dream. GL