anonymous
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anonymous
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Asked to leave ? A possibility especially if the CRL means approval after 2019. Did you hear if the plans is to offer at least 1 month severance ?
Settle down guys. No CRL yet but chance is high given the woes in Hayward. Blame TA in Hayward for fucking it all up as it was too late for TH and his cronies even with big pharma pedigrees to fix the absolute incompetences. Heard that TA having zero experience or vision tried to scale up prototype manual fill finish.
Sit back with some wine and bong hits cos it's gonna be ugly with well deserved heads rolling all over if we get the dreaded CRL.
Is this the reason for the hold up in hiring? I was contacted four months ago by a recruiter for a regional reimbursement director role. I had three interviews, completed the survey and....wait for it...nothing. In the meantime I just accepted another offer.
I'm sure this might be a good role and a great company but I've moved on!
Shit I'm worried because its impossible to get a straight answer out of these f*cks. Different story from the Hayweird rumor.
Is this the reason for the hold up in hiring? I was contacted four months ago by a recruiter for a regional reimbursement director role. I had three interviews, completed the survey and....wait for it...nothing. In the meantime I just accepted another offer.
I'm sure this might be a good role and a great company but I've moved on!
Good for you pal. That said any job in Intarcia is shitty and concerns are growing bout botched launch with no clear pathway and strategy from payers POV. At best MCOs will wait, demand more data not to mention rock bottom price in par with other pens and use Teva's generic exenatide (same as ITCA) to squeeze more out of GLP-1 purveyors.
Hello, late night calls. Hello, no shows. Hello, 1 claim and the malpractice insurance premium sky rocket. Hello, known and well documented nasty nausea side effects. Hello, pts demanding to remove foreign sticks from their tummy ASAP and conundrum of who will pay for the procedure with docs likely hung out to dry. Not worth it!I get it. Everyone thinks the payers will be the gatekeepers. Yes, provided primary care docs are willing to do the procedure to insert the device. I don't know any PCPs that routinely make sterile incisions on their patients. And yet everyone is convinced that by certifying a doc that they'll be doing these ten times a day. Perfectly, no less!
Hello, complications. Hello, botched jobs. Hello, liability insurance. Hello, infections. Hello, removals. Hello, prior authorization denials. Hello, claims appeals. Hello, hello? Anybody home on the 13th floor?
I'm outta here!
EXSCEL: No CV Benefit, but No Harm With Bydureon in Diabetes
Lisa Nainggolan
May 25, 2017
The Exenatide Study of Cardiovascular Event Lowering (EXSCEL) trial involved 14,000 people with type 2 diabetes at a wide range of cardiovascular risk, from 35 countries, and randomized them to once-weekly exenatide (2 mg subcutaneously) or placebo on top of usual care. Exenatide met the goal of cardiovascular safety but failed to show any cardiovascular benefit.
"Fewer cardiovascular events were observed in the Bydureon arm of the trial; however, the efficacy objective of a superior reduction in major adverse cardiovascular events did not reach statistical significance," AstraZeneca said.It adds that the full results of EXSCEL will be reported on September 14, at the European Association for the Study of Diabetes meeting in Lisbon, Portugal.
Showing CV Benefit Is the New Norm in Type 2 Diabetes
Therefore, the fact that EXSCEL has failed to show any cardiovascular benefit with exenatide when other trials of GLP-1 agonists have shown this to be the case will be viewed as somewhat disappointing. This failure is likely to reduce the use of exenatide for the treatment of diabetes.
Relax skippy. We are disruptive. We are all keyed up. We solve compliance.
Wait for our oral ! Oh yeah it's just a year away
Novo is working on a longer-acting product the company reported positive results from the Phase 3 SUSTAIN 7 study showing two doses of its once-weekly candidate semaglutide significantly outperformed Trulicity in lowering glycosylated hemoglobin levels. The company submitted a New Drug Application for subcutaneous semaglutide in December and is currently conducting a late-stage study for an oral version slated to complete next summer.
So forget calling me back. Yes it was fun waiting and waiting to hear. Thank God I stayed put.
Just proves that Intarcia is disruptive - to the stupid investors who have been sold a pile of shit
The greatest perils for Intarcia are within with nasty mean spirited politics and complete lack of trust in every levels. Never seen such dysfunction, angst, chaos and back-stabbing in a company. Most employees are just in it for the paychecks while looking to leave. Even very well paid army of consultants are looking for exists.
Wow your intelligence and piss poor spelling really shines thru chump and may I sat typical losers hired by Intarcia dumb ass.You are all jealous and mean. We are lucky to be a part of a new kind of biotech that is saving lives. Did you ever stop long enougnh to apreciate how much this means to be in on a whole new way to treat deseases. Please stop with the whining and complaining about something that you must be to stupid to unnerstand.