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***OFFICIAL CYDY/Leronlimab Thread*** (2 Viewers)

adonis said:
Some news that they’ll start enrolling folks in the UK for the s/c phase 3 trial that’s ongoing, apparently as part of their “fast track approval” request there.  
 

Also requesting BLA for HIV in the Uk within 4 weeks.

Oh, and they indicate they’ve submitted written questions to FDA for their type A meeting which will now be done in writing and responded to by Sept 4th rather than teleconference.
Click to expand...
So relatively good news which means a drop in the stonk. Otis will have to buy a LEGO polaris

 
Last edited by a moderator:
adonis said:
Some news that they’ll start enrolling folks in the UK for the s/c phase 3 trial that’s ongoing, apparently as part of their “fast track approval” request there.  
 

Also requesting BLA for HIV in the Uk within 4 weeks.

Oh, and they indicate they’ve submitted written questions to FDA for their type A meeting which will now be done in writing and responded to by Sept 4th rather than teleconference.
Click to expand...
Where you getting this? We get another video?

 
After Several Months of Providing Requested Information About Manufacturing and Safety of Leronlimab, U.K.’s MHRA Accepts CytoDyn’s Request to Enroll in its Current Phase 3 Trial for COVID-19 Patients with Severe-to-Critical Symptoms

:lmao:  that PR headline is amazing. Guess the new pro hasn’t started yet. 

 
Capella said:
After Several Months of Providing Requested Information About Manufacturing and Safety of Leronlimab, U.K.’s MHRA Accepts CytoDyn’s Request to Enroll in its Current Phase 3 Trial for COVID-19 Patients with Severe-to-Critical Symptoms

:lmao:  that PR headline is amazing. Guess the new pro hasn’t started yet. 
Click to expand...
Do they ever have a press release that doesn’t somehow make them sound incompetent? 

 
Capella said:
After Several Months of Providing Requested Information About Manufacturing and Safety of Leronlimab, U.K.’s MHRA Accepts CytoDyn’s Request to Enroll in its Current Phase 3 Trial for COVID-19 Patients with Severe-to-Critical Symptoms

:lmao:  that PR headline is amazing. Guess the new pro hasn’t started yet. 
Click to expand...
Should have taken out everything before the comma.

 
Capella said:
After Several Months of Providing Requested Information About Manufacturing and Safety of Leronlimab, U.K.’s MHRA Accepts CytoDyn’s Request to Enroll in its Current Phase 3 Trial for COVID-19 Patients with Severe-to-Critical Symptoms

:lmao:  that PR headline is amazing. Guess the new pro hasn’t started yet. 
Click to expand...
After being captured on security cameras sighing "I'm so tired of these ####ers, just push this through", U.K.’s MHRA Accepts CytoDyn’s Request to Enroll in its Current Phase 3 Trial for COVID-19 Patients with Severe-to-Critical Symptoms

 
Getzlaf15 said:
what was exactly said about this?

That FB post was taken down the other day because author didnt provide link/source
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For some reason when I quote I can’t paste via my iPhone, this board needs a RANTES bath. It was said that they are in comms with ows which is also very good news aka down 10%

 
Bluto Blutarsky said:
Dr P said they have been in touch and that both he and Cytodyn have been in email contact.  
 

no idea what it means because I have no idea what ows is 
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I believe I read that all biotech companies that were working on something related to covid had received some letter. Not sure where I saw that or how true it even is but not really exciting imo. 

 
  1. Dr Yo is solid.  If he could lose some of the immature things he does like the Ranties not Panties, he'd be on his way to getting a lot of respect.  Of course, he does need a bigger audience too but he's very smart and I believe he is a good career in front of him.
 
Dr. P’s paper got delayed originally because there was no control group, his answer to that was perfect. He said how can we give them a control when they are so sick and actually need treatment, it would be unethical to not treat them. This wasn’t pushed by the FDA but by the journals.

 
CGRdrJoe said:
Dr. P’s paper got delayed originally because there was no control group, his answer to that was perfect. He said how can we give them a control when they are so sick and actually need treatment, it would be unethical to not treat them. This wasn’t pushed by the FDA but by the journals.
Click to expand...
Much better explanation than the last time he just said it was “political”. 
 

Dr. Drew has seen the revised version and said if there’s an issue with that, someone needs to talk to the journals ethics committee. Drew actually seemed very impressed with what is in it. 

 
CGRdrJoe said:
Dr. P’s paper got delayed originally because there was no control group, his answer to that was perfect. He said how can we give them a control when they are so sick and actually need treatment, it would be unethical to not treat them. This wasn’t pushed by the FDA but by the journals.
Click to expand...
Sounds like they got their control group that will be published.  In the end, this should be a good thing and hopefully will bolster his theory and get some traction on it.

I still believe good things are coming for leronlimab/Cytodyn/IncellDX.  Its easy to get down on it right now as it's definitely stuck at the present moment, but this game is not over.

 
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