Hows the Chicago DM & Coherus to work for?

Discussion in 'Coherus BioSciences' started by anonymous, May 18, 2020 at 11:35 AM.

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  1. anonymous

    anonymous Guest

    Hi guys, any feedback would be appreciated ASAP. I've been in biotech for twenty years & now going through a downsizing---being recruited to Coherus. On a scale of 1-10, 10 being best, how would you rate Udenyca and Coherus to work for . THANK YOU.
     

  2. anonymous

    anonymous Guest

    It’s a contracted product, essentially a generic. All based on your payer coverage and what your current customer base is. This is not a salesman’s drug. The Chicago dm is a dolt but harmless. It will not help your oncology resume as biosims are not looked upon highly but if you’re looking to land it’s a simple job.
     
  3. anonymous

    anonymous Guest

    Run
     
  4. anonymous

    anonymous Guest

    This post is 2 years old. This poor bastard walks among us now and regrets every minute of it. Come join the resistance imbecile!
     
  5. anonymous

    anonymous Guest

    Why is the stock tanking with such a good pipeline?
     
  6. anonymous

    anonymous Guest

    Shitty management.
     
  7. anonymous

    anonymous Guest

    The stock is reacting to the
    (i) overall mkt selloffs (ytd: <-10%) due to Fed Fund Rate expected march to 2% from 50bps, by EOY;
    (ii) smart money rotating into value vs 'growtie' stock; and
    (iii) [specifically to this co] udenyca sales plumetted from >US400m (2020) to ~US320m (FY2021) mostly from price decline.

    Pipeline legit, but market being erratic assigning low probability for the successful commercialisaton of
    (i) FDA approved Humira-biosimilar (Exp:yearly sales >2023 US1bn, 10% mkt share, with potential to scale production up to 30%); and
    (ii) Udenyca-OBI/AI - Potentially capture ~50% Nuelasta-pro mkt (value: US0.5bn p.a.).

    If you share this insight then by. If not find another co and/ or exit position.

    May the force of evolution be w you.
     
  8. anonymous

    anonymous Guest


    Pipeline? You mean Yusimry? There are already 6 other humiras approved...this drug was stillborn from the moment the fda approved it, even though we refuse to admit it. Maybe you mean our lucenta biosim? Fun fact...nobody uses lucenta anymore bc its more invasive. What would the conversion of the miniscule market lucenta still commands do for us? Zero. Our only salvation is the on-body inj, and at best that gets us to maybe 30-35% of the neulasta market total for12-18 months...until theres a 3rd devise in the market. We are left with just biosims now & that business model has already been proven to be commercially unviable. Need proof? Novartis is dumping sandoz. The only hope for a future here was based upon a successful pivot into the pd1 market...already a long shot at best even with FDA approval being there are 6 others in the space. Now thats over. Nobody overcomes an fda crl, and if we do, itll be years down the road when nobody cares. We effectively need to rerun all our trials across all tumor types. Our stock peaked two years ago like others have said on here. Start looking.
     
  9. anonymous

    anonymous Guest


    You're right. This seems to be heading into a potential US50m - US150m cash crunch by Q1/Q2 2022, due to the fast declining Udenyca sales and high expenses.

    Even with the tranche C (req. FDA's approval for Toripalimab for drawdown) and D (req. FDA's approval for lucentis biosimilar for drawdown) from the new debt facility, there would likely be a significant shortfall (US50m).

    The new IB fella appointed to the board might be partly to 'conjure' up some financing. If that failed, Coherus might need to resort to right-size, and we all know what happened last time.

    For the time being, all facts point to shitville.
     
  10. anonymous

    anonymous Guest

    How about a strawberry flavored Yusimry?
     
  11. anonymous

    anonymous Guest


    Well said, well thought out. It’s incredible how fast cash flow is bleeding
     
  12. anonymous

    anonymous Guest

    Maybe it will help if Reider shaves his head more.
     
  13. anonymous

    anonymous Guest

    Folks stock hit Another all time low…red
    Flag warning, really is time to look out for one another - we took a chance and it failed, that’s ok.
     
  14. anonymous

    anonymous Guest

    I’m still waiting for that Reider head shaving thing to pay dividends.
     
  15. anonymous

    anonymous Guest

    Quick! Toss us more worthless equity to keep us. Hahah
     
  16. anonymous

    anonymous Guest

    We are just like Clovis and Puma now
     
  17. anonymous

    anonymous Guest

    No. Clovis and puma failed to gain approval of cutting edge drugs with totally new mechanisms of action. They took a chance to define markets. We failed to bring to market a 7th place pd1 retread that could be replicated by anyone with an IQ higher than their age. Big difference.
     
  18. anonymous

    anonymous Guest


    Such a doucher
     
  19. anonymous

    anonymous Guest

    "Dummy Lanfear is a process & manufacturing expert. It's what he did at Amgen, and look at that success. He is a saint!" Steve-o

    Apparently the FDA believes otherwise...
     
  20. anonymous

    anonymous Guest

    Denny save us? I hope it's not because of his motivational speeches. He speaks on stage like an ADHD addled Corky Thatcher. Guy could'nt get a rise out of Ron Jeremy with one of his pep talks. The spawn of of a cross between Neville Chamberlain and PT Barnum would be more trustworthy and believable.