Gordon Stein, CFO of CleanTech Lithium, explains why CTL acquired the 23 Laguna Verde licenses. Watch the video here.
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bull *****ers are better being called out than ignored!
Maybe he will purchase the 21 shares he was allocated in the placing?
Maybe he is sick of your constant deramping here Seb? Just a thought.....
I very much doubt that anyone reading his posts will be influenced in anyway Simmo. Maybe he will influence them to filter him though. I'm sure he is the most filtered poster on this board.
I'm having a nightmare here...forgive me its pre beer.
should be a full stop after "convinced". Treatments will be required,
Hi org....the market for SGN001 lives long past Covid 19 ....
ie COPD, asthma and other viral lung infections....along with Covid mutations.....
What Covid 19 has done for SGN001 is to accelerate the testing process to market...
GLA
Great "posts" Tams fat thumbs
Great post here folks , just back from a walk in the Dales Yockenthwaite whilst thinking about the next few months SP and vaccines.
One of the folks who won the Nobel prize this year for Physiology or Medicine for Hep B ID and research, in an interview the journalist (I paraphrase)mentioned that no Hep C vaccine has been found after 30 years work. However there are some very successful Treatment regimes that work against Hep C viral infection. The point I make is that vaccines may be ultimate cure but Covid 19 is a very tricky one and I'm not convinced , treatments will be required.
Hi Org, this is my very humble opinion and nothing more scientific.... an “ideal” vaccine would still take a very long time to roll out, a year maybe? Even RM is hoping this whole trial will be completed in two months, I can’t see it impacting the trial. Then hoping we do get an effective vaccine, we will still need treatments for the young, the old and the immune compromised. That’s me being positive about a vaccine.
In reality, I don’t think we will get a highly effective vaccine and even if we do many people won’t take it. Just review the board discussion this morning For people saying they won’t take it. The people on Here are very well educated and intelligent, if even these rational analytical people don’t want it, I can’t see the general take up being very high.
In my very personal view, I would take an experimental/new treatment if I needed it in hospital. I would not take a new vaccine when I’m otherwise healthy And no one knows the long term effects and long covid in particular. As I say personal view, nothing more.
Why would a vaccine have an effect on the SNG018 trial?
You are not going to vaccinate people who are in hospital that are in desperate need of some form of treatment now are you.
I believe that interim results can be looked by the independent committee after 100 patients in each arm. Can anyone confirm that?
If so, we could be looking at 5 patients in each of the 20 countries. Surely that could be filled in day(s)?
Calvert, we will have to wait and see!
Everybody will want to see interim results as soon as possible.
There may be some delay in setting up the trials in 20 countries, but then the cases should flow. 900 patients is only 45 per country. The UK admitted 1139 Patients to hospital yesterday, there must be a fair number at Osci level 4. We have legislation to shift a treatment fast if the UK regulator wants to.
I don’t think we can plan for it, we will know How fast they can do it until the RNS lands.
Is it practical, in all the current and near term prospective circumstances to plan for interim analysis of available results from a SNG Phase III trial by Christmas or 1 Jan?
Org I agree this a great board and fantastic posts. I’m not sure I agree about derampers. If you watch just before and during a share price dip, negative posters will turn up with really predictable “questions” or concerns. They clock off about 4.30. Just look at their posting history and it’s either A low number or a series of innocent negative questions.
Also I try to answer concerns where I have done some research because new PI’s do come here for more info. I have visited boards for new investments and well researched response can really help. It may not shift the share price, but it helps genuine PI’s, Not to mention the people new to investing.
Much more to come.
The company is run by some very smart people who know this industry inside out. Everything is being done for a reason.
The discussions with the FDA and other agencies/government bodies, at home trial, fundraising for phase 3, production of 100,000 treatments and discussions with partners - there is method behind all of these decisions.
There’s £6m set aside in the placing RNS appendix that has only been broadly explained.
“The Company is also discussing with a number of other research organisations and trial delivery groups in the UK and internationally as to how it could either commence trials of SNG001 or otherwise integrate SNG001 with existing trials.
C. £6m
“Generating further data to support SNG001 clinical development, manufacturing processes and regulatory activities”
MUCH more to come here!
I was actually just reading over the RNS on Placing and Open Offer again.
Even though it was only released just under 2 weeks ago, given what is happening in the world now with cases rising again, it's well worth re-reading.
The references to the FDA,EMA and NIHR make it clear that everyone who matters is aware of this trial and the potential implications.
"On 14 October 2020 the Company was informed by the National Institute for Health Research (NIHR) that the Phase III trial has been badged in the UK as Urgent Public Health and will be recognised as a National Priority study. Notwithstanding this, the commencement of the trial will still be subject to normal regulatory and ethical approvals."
I suspect there will be a lot happening in November and December. Everyone wants and needs this to be a success.
Also worth noting that although the IND to FDA usually takes 30 days,this can be shortened.
"Upon receipt of an IND application, FDA will notify the sponsor of the date it receives the application through an IND acknowledgment letter.
An IND application may go into effect:
30 days after FDA receives the application, unless FDA notifies the sponsor that the investigations described in the application are subject to a Clinical Hold; or
on earlier notification by FDA that the clinical investigations in the IND may begin. "
I'm the same WPA.
I don't expect there to be a lot of movement on the SP until there is more news to be announced. We may move 10-20% or so either way of the current SP but news could drop at anytime and then anything could happen. I wouldn't want to be sitting with nothing if/when the SP takes off.
"next" update
... is a first for me with any share and, if Ishould need any reassurance it's a quick look back at the daily, after hours buys , day after day that 'keeps it real' for me. Looking forward to seeing my full share 'allowance' being added , digesting the presentation update and seeing this start its inevitable climb. Roll on end of the week and into November, and beyond. Tick tock.