I need an update on this.
The company hasn't released any new info yet but based on what the CEO said in his last update I think we COULD be about 3 months away from the trial starting. In his last update the CEO said that the disaster with the cell company he was trying to work with delayed things by about 6 months. Since that trial was supposed to start BY December 2019 that means that he COULD be able to start a trial by roughly June of 2020. After all, 6 months from December 1, 2019 is June 1, 2020.
I’ll believe it when I see it. Don’t trust anything this CEO says anymore.
Exactly. There's literally nothing else for them to do. With Tsuji we don't even know if they are still researching ways to improve their technology. They should've been in human trials by now, but we haven't heard anything. At least here we know that the research is done by Tissuse, and J Hewitt is solely responsible for carrying out trials and commercializing it. Since it's in J Hewitt's hands already we know that the next obstacle is just the logistics of carrying out the first trial. They will get it done one way or another, it's just taking longer than hoped.
Tsuji and TissUse will take at least 5 years to come to market if they start their trials today. Neither have conducted a Proof of Concept or Phase 1 trial. You need to finish Phase 2 to commercialise
You need a life. Wait for tsuji. He will get ya one for sure.You need help.
"It is five years since Japan passed laws regulating stem-cell clinics; in that time, some 3,700 treatments have received the green light. From Hokkaido to the islands of Okinawa, companies in Japan can extract stem cells from skin biopsies and use them in injections for complex conditions such as heart disease.
But the vast majority of these therapies have not passed a randomized, controlled, double-blind clinical trial, the global standard to prove that interventions are safe and effective, and the foundation for most medical regulation. Instead, Japan’s 2014 Act on the Safety of Regenerative Medicine and a second law, the 2014 Pharmaceutical and Medical Device Act, provide a fast track to market approval."
https://www.nature.com/articles/d41586-019-02844-6
A recently approved stem cell treatment approved before trial data was even published:
"The clinical trials that demonstrated efficacy were based on only 13 participants. There was no control group and the trial data remain unpublished."
https://www.nature.com/articles/d41586-019-00332-5
In a recent email I've been able to see, TissUse said they still expect to have trials conducted this year and that the procedure will reach "market maturity" within a few years. Market maturity is when sales begin to grow at a decreasing rate. If that's really what they expect, then I interpret that as they expect to commercialize it very quickly after the first trials are completed (if successful). They also hinted at pursuing trials and commercialization in Europe again.
They may have meant something else by “market maturity”. I find it hard to believe that sales would already be declining a couple years from now.
Probably. Don't know what, though. Sloppy, unclear words as usual.
Still, though, if trials are done this calendar year, and the results are satisfactory and a company or companies want to sell it publicly, there's really no reason it couldn't be available next year. How long wait times are is another story.
What do you mean?Seems like SHISEIDO has so much faith to stop cell company’s working with J hewitt
What do you mean?
Shhhhhhh shut up insect!.It's OK to be a cocksucker.
Don't keep it in, sister.
Come out of the closet.
You'll find a beautiful man, settle down and have a big family in the suburbs...