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Stock Thread (9 Viewers)

SFY into the green.  Just placed a 1% trailing stop loss to lock in those profits for the day.

 
Depends on whether you bought and how many
I was gonna bump my $4.9 to $5... 

At the open, I was on the grill making some serious breakfast sammies for the fam, opened it we were $5.5 heading south quick and I thought $4.65 was going to be where it was bought.

Nonetheless, call was absolutely on point and I’m a greedy idiot!

 
I was gonna bump my $4.9 to $5... 

At the open, I was on the grill making some serious breakfast sammies for the fam, opened it we were $5.5 heading south quick and I thought $4.65 was going to be where it was bought.

Nonetheless, call was absolutely on point and I’m a greedy idiot!
I increased my position 12% on the downward slide. Avg. price about 5.44

 
Scary that they can dump shares like that and cause a $1.25 drop...... but the fact that it snap rebounded is a relief
Still down 7% on a day where they release pretty good news for a drug that can be used to treat the worlds most pressing disease right now.  

 
I don’t know how I could day trade without being retired. Some of this stuff moves so much during the day. I’m good with the shares I have. Not going to get greedy unless I see it fall later.
Most of the movement happens, with CYDY, within the first 30 minutes of opening, and then in the last couple hours.  From what I hear, that's true of much of the market...first couple hours, and last couple hours generally.

 
noob question... 

CYDY

im using ameritrade i have around 2k shares. i want to sell some but am unsure on when the funds will be 'cleared' so i can buy again?

last time i tried this i got a nasty email saying i cannot use uncleared funds more than a few times per X amount of months

 
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Still down 7% on a day where they release pretty good news for a drug that can be used to treat the worlds most pressing disease right now.  
Happens after running from $2.70 last week and being up 15-16% yesterday. While good news, not the full set of data so still risk.

 
Can it? 
 

The release said the drug won’t harm you... that’s it
That's not it.

It reduced the SAE's overall, and the SAE's that remained were said to not be related to leronlimab.

So not only does it not increase SAE's like remdesivir, it decreases them overall and doesn't add any on its own.

In order to decrease SAE's versus placebo, how do you think that happens without efficacy in reducing the severity of the disease?  The question is how efficacious is it, not whether it is or not.

 
I'll be doing the same.  I suspect there will be a sharp pullback and choppy trading today.  I'm sure the shorts are primed to pounce.


sigh. I'm counting on the typical investor being a bit more skilled in interpreting these results.


I'm hoping there is weakness shown, as I would love to buy more. 

But I am afraid $8 will be the closest we see to weakness today


I think it open around 8. I think it goes beyond, but many variables besides the stock's value can impact that, including but not limited to: press reaction, short sellers, FED printing money and many others.

These result warrant a minimum of a 20% bump and as crazy positive as the market has been to positive COVID news it could go significantly higher.
I guess the typical investor wasn't more skilled.....

 
That's not it.

It reduced the SAE's overall, and the SAE's that remained were said to not be related to leronlimab.

So not only does it not increase SAE's like remdesivir, it decreases them overall and doesn't add any on its own.

In order to decrease SAE's versus placebo, how do you think that happens without efficacy in reducing the severity of the disease?  The question is how efficacious is it, not whether it is or not.
We know there is a benefit, very likely substantial to the only approved treatment, this stuff takes time. I’m comfortable in my position.

 
That's not it.

It reduced the SAE's overall, and the SAE's that remained were said to not be related to leronlimab.

So not only does it not increase SAE's like remdesivir, it decreases them overall and doesn't add any on its own.

In order to decrease SAE's versus placebo, how do you think that happens without efficacy in reducing the severity of the disease?  The question is how efficacious is it, not whether it is or not.
IMO it's not a large enough sample size that the SAEs mean diddly.  The efficacy better be through the roof or we are looking at another trial that will take months to fill.  In the mean time big Pharma will get their treatments approved and we'll be talking about hope for cancer.

 
That's not it.

It reduced the SAE's overall, and the SAE's that remained were said to not be related to leronlimab.

So not only does it not increase SAE's like remdesivir, it decreases them overall and doesn't add any on its own.

In order to decrease SAE's versus placebo, how do you think that happens without efficacy in reducing the severity of the disease?  The question is how efficacious is it, not whether it is or not.
We know there is a benefit, very likely substantial to the only approved treatment, this stuff takes time. I’m comfortable in my position.
If it gets people out of the hospital faster than remdesivir, and it's safer, its' a home run.

 
Adam Feuerstein is a despicable human:
I think the lack of efficacy data is a fair criticism. My bigger issue is he seems to move the goalposts depending on who he is writing about. If it's about GILD, he'll pump it up on positive data from one hospital. Similar with MRNA, nobody put them under a microscope. 

 
In the meantime....Blmn ran to $10.70 (I stop lossed at 10.54) and is not back down to 10.35 for those looking for an entry point.

 
I think the lack of efficacy data is a fair criticism. My bigger issue is he seems to move the goalposts depending on who he is writing about. If it's about GILD, he'll pump it up on positive data from one hospital. Similar with MRNA, nobody put them under a microscope. 
Yes, he’s a paid shill, we know this. His writings become meaningless over time. He’s gotta go find a new ticker where the strong hands aren’t as familiar with him.

 
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IMO it's not a large enough sample size that the SAEs mean diddly.  The efficacy better be through the roof or we are looking at another trial that will take months to fill.  In the mean time big Pharma will get their treatments approved and we'll be talking about hope for cancer.
Not a large enough sample size based on what?  

If you set the experiments up correctly, you can get meaningful data with smaller populations.  This was a quality study and the results are quite good.  Statistical analysis will be used to determine what differences in population can be attributed to randomness, vs the effect of the drug.  

 
Efficacy doesn't need to be through the roof, it needs to be statistically significant. If it comes in with a p-value of 0.01 or better, and with good safety, the medical community will love it. If it comes in say around 0.04 or so, that is still significant but will have a few looking for more data still. To me the way they are dripping out the info is not ideal, but they almost had to because of how they've been teasing results for so long (and occasionally missing some soft "deadlines" they set for themselves). I'd personally prefer they not release anything else until they have the analysis done on both the primary AND secondary endpoints. Then you can release it all at once and tell a complete story - good, bad, or mixed. 

That being said, I think that the interpretation that the SAEs are positive in their own right and hinting at efficacy is sound - but we can't know for sure until we see the rest of it. 

 
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Efficacy doesn't need to be through the roof, it needs to be statistically significant. If it comes in with a p-value of 0.01 or better, and with good safety, the medical community will love it. If it comes in say around 0.04 or so, that is still significant but will have a few looking for more data still. To me they way they are dripping out the info is not ideal, but they almost had to because of how they've been teasing results for so long (and occasionally missing some soft "deadlines" they set for themselves). I'd personally prefer they not release anything else until they have the analysis done on both the primary AND secondary endpoints. Then you can release it all at once and tell a complete story - good, bad, or mixed. 

That being said, I think that the interpretation that the SAEs are positive in their own right and hinting at efficacy is sound - but we can't know for sure until we see the rest of it. 
Good posting.  Agree it would have been better if NP would have been able to release all endpoint data.  But anyone who knows or has (painfully) followed NP's interviews and PRs, understands he means well but sometimes can't keep his foot out of his mouth.  Consciously or not, he says things that are interpreted as promises and many end up not coming to fruition.  I think the safety data are good and does, in turn, hint to positive efficacy data.  But we'll have to wait and see.  

 

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