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CUV, CLINUVEL PHARMACEUTICALS LIMITED
waz
post Posted: Today, 09:19 PM
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In Reply To: FarmaZutical's post @ Today, 07:34 PM

This leads directly into the description of the recently granted patent where it states the compounds in particular benefit immunocompromised patients (in addition to the general public).

This was a Phase II trial. Would not be surprised therefore that at some stage, hopefully soon, results will be released. There are surely other trials where information was never released - this has been going on for 13 years. Dr Dennis Wtight key person in CUV1647 study.
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FarmaZutical
post Posted: Today, 07:34 PM
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One of the clinical trials that I have been most
interested in throughout the years is
CUV011 with 200 participants aimed to evaluate
Scenesse in AK/SCC in organ transplant recipients.

https://clinicaltrials.gov/ct2/show/NCT00829192

It had an end date in 2012 but results were never reported.
I’ve wondered for a long time if it was classic Clinuvel behavior
burying bad results or if there was indeed a strategic reason
for not reporting.

The principal investigator was / is Günther Hofbauer and in this article from
December, 2014 he states, that “studies are currently underway,” suggesting that
the trial was ongoing at that time.

https://serval.unil.ch/resource/serval:BIB_...87D78D.P001/REF

With the renewed focus on DNA repair and general protection against skin
cancers the AK/SCC OTR trial could be a centerpiece, I think.

Was it a failure, was it a success, was it still ongoing in 2014, is it still ongoing
today, was it finished and just waiting to be published at the right moment ?
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Said 'Thanks' for this post: PortugueseMan  IntiRaymi  waz  PunkassDerm  
 
the near future
post Posted: Today, 05:48 PM
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In Reply To: garthyd's post @ Today, 04:58 PM

As you said, it can not last

SP is a joke at the moment, very cheap

Big new investor might join the party soon





Said 'Thanks' for this post: waz  
 
garthyd
post Posted: Today, 04:58 PM
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In Reply To: the near future's post @ Today, 04:36 PM

In only a month, our 12 month low will be $21......which its pretty unfathomable to think we could be at 12 month lows after FDA approval......It can't last.

 
the near future
post Posted: Today, 04:36 PM
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In Reply To: garthyd's post @ Today, 03:16 PM

Nobody is selling, rather people are buying at this low sp price

the short sellers seems that they sold most of their shares, waiting to buy back

I hope we bottomed now, and short squeese will happen with any upcoming news





Said 'Thanks' for this post: waz  
 
garthyd
post Posted: Today, 03:16 PM
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Gotta be one of our lowest volume trading days in months?

 

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Fortescue Bullro...
post Posted: Today, 11:55 AM
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Just ordered 2k at market. Very encouraged by all I am reading the last few days, and LHFUD receding in the rear view mirror. Thanks sharelooker, waz and all here.
Got them at 26.038.


Said 'Thanks' for this post: the near future  Alaaf  waz  
 
trisail
post Posted: Today, 11:48 AM
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Friday 6th Dec on the ASX only 50,530 of the total volume of 164,852 shares sold were short sales. Some profit taking maybe?

 
waz
post Posted: Today, 10:16 AM
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New director buying shares on market - bought at $27.43. Would be good to see more director buying on-market. Don't stop now.


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waz
post Posted: Today, 09:03 AM
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In Reply To: IntiRaymi's post @ Today, 06:14 AM

My read is that CUV has in recent months sought to update and finalise this patent and a separate XP related patent. There appears to be some finalisation of the compound description in particular plus refinement over claims.

There is wide coverage in application and while these patents have been in progress some time this all seems to be a precursor to CUV getting cracking on the wider application of afamelanotide now that FDA approval is in place.

Finer points in PW's AGM and other recent monologues indicate the real action with the compound is now moving ahead. I am expecting this to occur on all fronts - Vitiligo, VP, XP and in particular DNA repair, where once ethics approval is obtained from the FDA the 20 person clinical trial can be agreed upon, populated and commence. I believe CUV already know the answer but obviously need the programmed clinical evidence to obtain the further approval needed for DNA repair compounds in treatment and prevention of skin cancers.


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