rosemountbomber
2 weeks ago
Well, now that we have surpassed and made a new 52 week high, we can attack the 104 week high at just under $12.50.
As always seems to be the case for me, I worry that just at this starts moving north, the overall market in some sectors is so overvalued that some are
talking about some sizable profit-taking for the market as a whole. Hope it doesn't affect us here or some other stocks that I have that I consider undervalued.
Big volume yesterday, hopefully continues today.
Whalatane
4 weeks ago
Thx Jess but I think Lupy is still seen as " when all else fails ...try Lupkynis "
This is primarily because of its pricing and the road blocks insurers put up to try and avoid paying for it .
Benny is significantly cheaper , is a sub Q , does not allow as fast a steroid taper as Lupy ...but because its some much cheaper insurers often want patients to try that first
The drug ( Lupkynis ) faces competition from GSK’s Benlysta (belimumab), which received FDA approval slightly earlier in December 2020 and EMA approval in May 2021. Despite Benlysta being a subcutaneous treatment, it is projected to outpace Lupkynis in sales by 2030. According to GlobalData’s Pharma Intelligence Center, Lupkynis is expected to reach $447m in sales by 2030 while Benlysta is forecasted to generate $1.76bn.
AUPH has slashed payroll so major cost saving there and Tang is probably trying to get the Co ready for a sale
Good luck
Kiwi
Whalatane
1 month ago
Well Jess you can review all my posts on Ihub ....boards posted on etc ...and review my positions on APP, RZLT , SWAV , SLNO etc .
APP and RZLT I still hold .
SWAV was bt out and selling SLNO ( up about 7X at time of sale ) was a huge mistake ( as I've noted )
Re AUPH , KZR , UNCY and ARDX
I'm not negative on AUPH . I think I responded to a post from Cosa some time that if I owned it I probably wouldn't be selling it .
However I'm not super positive on it and think theres limited upside .
Re KZR vs AUPH ...the early data on KZR IMHO looked better . But Co ran into mgt / BOD issues and eventually adverse events torpedoed the stock .
I posted long ago why I was exiting KZR
UNCY and ARDX
CMS appears determined to sink any opportunity for dialysis patients to be prescribed these new serum pho lowering drugs .
Yes they may have access to them , but the way the dialysis bundle works ( providers get to keep any $ left over between what CMS pays per dialysis ...about $273 .. and what they spend ) essentially means that dialysis providers won't prescribe the new Brand pho lowering drugs because of the expense of these new drugs .... and will push the low cost generics instead .
This will change if the Kidney Patient Act pass's
I expected UNCY to rally on FDA approval of its NDA ...Instead the mkt sold the news .
So I was very wrong on that
Kiwi
rosemountbomber
1 month ago
A Fierce Pharma article dated today about the restructuring, (As a side note, I didn't know that sales were flat from 2Q to 3Q so I will have to go back and look at that again):
https://www.amazon.com/YOGINGO-Pack-Christmas-Stockings-Personalized/dp/B0D86JV9ZQ/ref=sr_1_41?crid=1M8FRWGP1DKNR&dib=eyJ2IjoiMSJ9.P8XAFzm46Eai6mU0rxi3J657M6xzme7YFrtWeGO8Ahf5iEyxaa59x5UEfo2Pv8ou-RabXdTMjVcejZZbdETKHNdygdyXHKxl3FfdVnbe37_D9DIhEzbXxH_Y_3X2D3yhJ8hB3G35XqSNC8s-KwqGY0-YtcJAX61IcWZ3f5CCGjV6NMH9Q2hRVb2_YkHUwdBtFjDswLBWzLX37K9qkZGoRXr1XFshtSY2Jebev6a2fHYA77wocgoYlpiDeLzCMls71OzOwlD96yOHCo95Z26K0puFLkBiC_h6ptHEKLvSwUQ.AF18_HCbKa0FQd125MB3rir03ZFnegC_Hx0_-2CkKvI&dib_tag=se&keywords=christmas%2Bstockings&qid=1731015416&sprefix=christmas%2Bstocking%2Caps%2C191&sr=8-41&th=1
"After an activist investor revolted against the leadership team at Aurinia Pharmaceuticals, the CEO in question is resorting to restructuring.
Aurinia on Thursday unveiled a strategic overhaul that will slash 45% of the Canadian biotech’s entire workforce.
Aurinia expects the trimming will save it more than $40 million in annual operating expenses. The move will allow the company to focus on the commercialization of its lupus nephritis drug Lupkynis and the development of AUR200, an autoimmune disease candidate that Aurinia recently salvaged from its garbage can.
The cost savings will strengthen Aurinia’s financial position and “provide more flexibility to engage in future business building activities,” CEO Peter Greenleaf said on an investor call Thursday.
This marks the second round of layoffs at Aurinia in less than a year. Back in February, following a fruitless search for a potential buyer, Aurinia decided to reduce its headcount by about 25%.
At that time, Aurinia had decided to discontinue AUR200 but later revived the APRIL/BAFF inhibitor. Now, CEO Greenleaf in a Thursday statement said the organizational overhaul will help Aurinia accelerate the development of AUR200, an “important pipeline product.”
Greenleaf’s leadership at Aurinia was put into serious question when he and three other Aurinia board directors lost majority stockholder support during the company’s annual meeting. The company’s proposed executive pay packages also failed to garner majority investor backing.
As required by Aurinia’s company policy, the four directors submitted their resignations. But the board, while accepting the resignations of the other three members, argued that “there are exceptional circumstances that warrant the rejection of Mr. Greenleaf’s conditional resignation,” it said in a September securities filing. As a result, Greenleaf stayed on.
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Investor activism resurfaces at Aurinia after CEO’s board role, exec pay lost majority support
Amid broader investor disapproval of Aurinia’s leadership team, an activist shareholder who owned 2.2% of the company’s stock in August called for board and management changes, blasting them for “unchecked spending, ineffective leadership, and a clear lack of strategic direction.”
Lupkynis is currently Aurinia’s single commercial product, with third-quarter sales of $55.5 million. The number represents 36% year-over-year growth but is flat compared with $55 million in the second quarter. The number of patients on the therapy has grown about 25% to 2,422 as of the end of September, Greenleaf told investors on a call Thursday.
“This significant year-over-year growth was driven by patients restarting Lupkynis after being off therapy for an extended period of time, as well as hospital fills and maintaining high persistency rates year over year,” he said.
With total product revenue of $158.6 million in the first nine months of this year, Aurinia has kept its full-year guidance range of $210 million to $220 million.
As to AUR200, the company in September dosed the first participant in a phase 1 single-ascending dose study, with data expected in the first half of 2025. Aurinia has not disclosed the indications that it plans to develop AUR200 in. "