Member Info for Nolupus

Splodge,

Dbv should get approval once the FDA have been reassured about the adherence of the patch ... The EMA have no problems with the efficacy of the adherence so we will see what happens in the very near future ...

I am sure most sufferers would prefer to just get a vaccine jab if one was available but the timeframe involved from the preclinical to the end of a P3 is at least 5 years IMO and would have to have HUGE money invested

Best of luck to all

Dallo,

Anything could happen but as you know well, IMM has a history of making lots of promises yet have never delivered on anything , IMO
Great story but rarely a happy ending is my view but one never knows ....

https://otp.tools.investis.com/Utilities/PDFDownload.aspx?Newsid=1463693

Breaching 80p

Chill. =. Sit back and wait :-)

Only after breaching will I put the champagne in the fridge and won’t open it until we get past 150

That’s called patience

Icarus42,

The market is the market and the SP is where it’s at because of shareholder lassitude of delays and NO proper communication or trust in management , imo

That could all change with one decent RNS but shareholder patience is well and truly tested

Dallo,

A buy out whilst a possibility is imo wishful thinking at this stage ...

IMM needs to advance it’s pipeline and FAST , imo

This radio silence is deafening....

Brh moving up nicely since yesterday

Took a punt this morning ....

Let’s wait and see

Brh is worth watching , ready for news , imo

Will we get some news or not ?

BRH. Idem ....

64—-70—-??

207....

Needs another leg up so I can sell with my punt margin :-)

Let’s wait and see

Supermobileman ,

If one considers that a clinical trial is just about the treatment period well so be it ....

I consider that a clinical trial is split into multiple categories and not just first patient treated , last patient treatment ....
1 ) administrative , Designing of the trial , requesting and gaining regulatory approvals
Recruiting clinical sites/ hospitals / etc

The recruitment of patients
Treatment time
Follow up and statistic readout
Top line results
Full readout of results and submission of results to the regulatory authorities....

Some may wish to ignore the process and focus on just the treatment timetable , but that is not my focus

Riseup,

Here is the latest news

https://valneva.com/press-release/valneva-initiates-phase-3-clinical-trial-for-its-inactivated-adjuvanted-covid-19-vaccine-candidate-vla2001/

https://www.clinicaltrials.gov/ct2/show/NCT02504645?term=Immupharma&draw=2&rank=2

June 2015. To April 2019.

Let you count the number of months

Easy to say BS but when you’re asked to put up or shut up .... again only BS ...

If you really wanted the truth and not just doing your usual personal attacks you would find the information on the clinical trial website ....

Super mobile man,

Why don’t you tell us how long it took Imm to do the last P3 trial if you know so much ??

Pff ,

Don’t you just love it when the newbies know more than anyone else ....

Well , when you go and do your own research , please come back and enlighten us ....

Tils , is heavily manipulated imo
Just take a look at the closing today :-)

At this SP , I would be a heavy buyer but everyone to their own views ....

85 p at the close today