CamPath 1H in MS


Anonymous

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Lemtrada???? What the hell kind of name is that???? Campath has a long history, dating back to the 80's @ CAMbridge PATHology and Dr. Herman Waldmann. MS was one of the first disease states that CamPath was investigated in and was the first commercially available humanized monoclonal antibody. Genzyme came onboard many years later when the proof of concept was already established in MS and has been trying to kill off the drug in CLL since it aquired it from Bayer. Patient advocacy groups in MS are up in arms about your intended manipulation of Campath and the huge price increase that you intend to put on it. Shame on you Genzyme.

Dec. 20 (Bloomberg) -- Genzyme Corp., the target of a hostile takeover by Paris-based Sanofi-Aventis SA, is spending more than $2 million a week to develop alemtuzumab for multiple sclerosis, Chief Executive Officer Henri Termeer said today.

Currently approved as a therapy for blood cancer and sold under the name Campath, alemtuzumab produced revenue of less than $150 million last year, according to Cambridge, Massachusetts-based Genzyme. The company predicts sales of $3 billion to $3.5 billion by 2017 with an added use in multiple sclerosis, and expects to see the first results in six months from the final stage of clinical trials. Mark Schoenebaum, an analyst with ISI Group Inc. in New York, estimates peak sales of $2.3 billion.

Sanofi on Dec. 13 extended the deadline for Genzyme’s investors to tender stock at $69 a share, or about $18.5 billion, to Jan. 21, 2011, from Dec. 10. The French drugmaker took its offer to shareholders on Oct. 4, after Termeer spurned the bid as too low, in part because it failed to consider alemtuzumab’s future value. Sanofi cites analysts’ estimates for peak sales of the drug from multiple sclerosis of $700 million.

“Alemtuzumab for MS is probably the largest single program we’ve ever undertaken,” Termeer said today at a meeting with shareholders in New York. “We’ve been investing more than $2 million a week to get to where we are today.”

Genzyme declined 14 cents to $69.65 at 4 p.m. New York time in Nasdaq Stock Market composite trading.

New Name

The company said today the medicine will be marketed for MS as Lemtrada, a combination of alemtuzumab and the Spanish word for “entrance.”

Genzyme and Sanofi have discussed a clause known as a contingent value right, or CVR, structured around Lemtrada, under which Genzyme stockholders would receive more money from the French drugmaker if sales goals are reached.

“CVRs are useful because people take different views,” Termeer told reporters today after the presentation. “Shareholders have been very supportive of the CVR idea.”

Jean-Marc Podvin, a spokesman for Sanofi, declined to comment.

Termeer estimated about a quarter of Genzyme’s current shareholders are short-term investors who bought the stock after Sanofi made its offer.

“Most bought at $71 or $72 a share,” Termeer said. “They don’t want to sell at $69.”
 

This is not shame on Genzyme. The market dictates the price. If the new therapies from Acorda and Novarits can get the $$ and do half as much as Campath, why would the market not allow Genzyme to do just as well?

What is a shame is that Americans are getting screwed by paying the highest prices in the world for the same therapies that others pay a fraction. We vote for it because we don't understand the reality of how the system works. There is no shame on Genzyme, how about shame on American ignorance for allowing a corrupt system.
 
Quit smoking that pipe, campath is a 3rd line agent, no one's using it right now, how big is the patient population anyway....you Bayer rep also believe that the leukine market was going to turn around too.....from 0 percent to 2 percent market share
 
Quit smoking that pipe, campath is a 3rd line agent, no one's using it right now, how big is the patient population anyway....you Bayer rep also believe that the leukine market was going to turn around too.....from 0 percent to 2 percent market share
and Clolar and Mozibil are blowing the doors off??
 
what patients? You're chasing down 17p deletion patients?....and docs are afraid of cmv
Everyone seems to forget that Campath has a front line indication and CMV is rare in those patients. The real shame here is that Genzyme has been planning Campath's demise in CLL since 2007 so it could rape MS patients. That's why Genzyme has never promoted it in the frontline setting. Another thought-Bayer Schering holds the rights to Campath in Solid Organ Transplant and is moving ahead in that area with no intention on changing it's name.
 
Everyone seems to forget that Campath has a front line indication and CMV is rare in those patients. The real shame here is that Genzyme has been planning Campath's demise in CLL since 2007 so it could rape MS patients. That's why Genzyme has never promoted it in the frontline setting. Another thought-Bayer Schering holds the rights to Campath in Solid Organ Transplant and is moving ahead in that area with no intention on changing it's name.

planning campath demise? Bayer sold it through 2009 and did not manage cmv side effects...oh yea that pesky virus and the tests associated with it, really rare? OK

remember the IV vs sq story, and label is what again? and you were pushing sq with no data......

3rd line my amigo with newer drugs coming in

raping ms patients? heard of a once a year dose?

solid organ and campath? really, heard of delayed organ rejection?

you've been drinking the bayer cool aid my friend......it's time to move on before they can your ass
 
planning campath demise? Bayer sold it through 2009 and did not manage cmv side effects...oh yea that pesky virus and the tests associated with it, really rare? OK

remember the IV vs sq story, and label is what again? and you were pushing sq with no data......

3rd line my amigo with newer drugs coming in

raping ms patients? heard of a once a year dose?

solid organ and campath? really, heard of delayed organ rejection?

you've been drinking the bayer cool aid my friend......it's time to move on before they can your ass
Bayer and Genzyme began negotiations for Campath in 2007. At that time the plan was to pull it back in anticipation of a MS indication. Frontline CMV viremia reactivation was 16%, easily treatable with oral gancyclovir. CMV test is a simple blood test. If you look at Rituxan, you could have HepC reactivation, and even worse, PML. I'de take the CMV. SubQ is the accepted way of giving Campath, so what's your point? Campath has indication of frontline through refractory, not 3rd line. MS dosing looks like it will be 15mg/day for 5 consecutive days/year. Campath has been used since the 80's in SOT with acute rejection rate of 15%, which is similar to ATG. Literature search of Campath and "delayed organ rejection" came up with nothing, I think you pulled this one out of your ass. I don't know who's koolaid you've been drinking, but you've had way too much. Do us all a favor and know what you're talking about before posting.
 
Bayer and Genzyme began negotiations for Campath in 2007. At that time the plan was to pull it back in anticipation of a MS indication. Frontline CMV viremia reactivation was 16%, easily treatable with oral gancyclovir. CMV test is a simple blood test. If you look at Rituxan, you could have HepC reactivation, and even worse, PML. I'de take the CMV. SubQ is the accepted way of giving Campath, so what's your point? Campath has indication of frontline through refractory, not 3rd line. MS dosing looks like it will be 15mg/day for 5 consecutive days/year. Campath has been used since the 80's in SOT with acute rejection rate of 15%, which is similar to ATG. Literature search of Campath and "delayed organ rejection" came up with nothing, I think you pulled this one out of your ass. I don't know who's koolaid you've been drinking, but you've had way too much. Do us all a favor and know what you're talking about before posting.

Easily treated yet the oncologists aren't using it.........you don't have data for sq if you did it would label.......what's the uptake of campath in SOT?.....another leukine story...have label for aml but no one's using it..........do you know how to use pubmed? Transplantation. 2007 Oct 15;84(7):821-8.
Alemtuzumab induction in deceased donor kidney transplantation.
 
Easily treated yet the oncologists aren't using it.........you don't have data for sq if you did it would label.......what's the uptake of campath in SOT?.....another leukine story...have label for aml but no one's using it..........do you know how to use pubmed? Transplantation. 2007 Oct 15;84(7):821-8.
Alemtuzumab induction in deceased donor kidney transplantation.
To PP-I'm reading this and saying to myself that you are either the competition or a disgruntled ex-employee, because no matter what anyone says you are going to rebute it. CMV is easily treatable, a simple straightforward statement that can't be denied. Same is true with sub q administration; considered the preferred path of administration by the medical community and payed for by the insurance providers w/o exception. I use Pubmed everyday and couldn't find the term delayed organ rejection and Campath in a single citation; I think you need to work on your terminology skills. ACUTE REJECTION was addressed by someone yesterday. Here's the take away message from the article you cited - "Alemtuzumab recipients receiving FK or CSA, MMF, and steroids had increased graft and rejection-free survival over 24 months compared to no CNI, MMF, and steroids. Conclusions. Despite reduced early rejection, acute rejection rates at 6 months and 1 year with alemtuzumab induction exceeded other forms of induction therapy."
 
To PP-I'm reading this and saying to myself that you are either the competition or a disgruntled ex-employee, because no matter what anyone says you are going to rebute it. CMV is easily treatable, a simple straightforward statement that can't be denied. Same is true with sub q administration; considered the preferred path of administration by the medical community and payed for by the insurance providers w/o exception. I use Pubmed everyday and couldn't find the term delayed organ rejection and Campath in a single citation; I think you need to work on your terminology skills. ACUTE REJECTION was addressed by someone yesterday. Here's the take away message from the article you cited - "Alemtuzumab recipients receiving FK or CSA, MMF, and steroids had increased graft and rejection-free survival over 24 months compared to no CNI, MMF, and steroids. Conclusions. Despite reduced early rejection, acute rejection rates at 6 months and 1 year with alemtuzumab induction exceeded other forms of induction therapy."


Author's conclusion -Despite reduced early rejection, acute rejection rates at 6 months and 1 year with alemtuzumab induction exceeded other forms of induction therapy.

campath kills kidneys
 


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