It, has been over a year now that the compassionate drug use Ipilimumab was terminated due to production problems. As a chemist working in the field of biologics, I know it only takes about 3 months to generate Human Monoclonal antibodies. So why is it taking so long? I know you are trying different production protocols, but patients are loosing hope and their lives waiting for this drug. Will the compassionate use be reinstated soon? You say in your mission statement that:
“What sets us apart? We believe it's our commitment to patients with serious diseases, our focus on finding innovative medicines that combat those diseases, and our dedication to extending and enhancing human life.”
We need you Help Now!!!
Response:
Dear Mr. Breitfeller,
Thank you for your email.
As you are aware, Bristol-Myers Squibb and Medarex had to suspend enrollment of new patients into the compassionate use program and single patient exemptions to ensure treatment is not interrupted for patients currently receiving ipilimumab and to provide supply for ongoing clinical studies.
The manufacturing cycle time and testing of a biologic such as ipilimumab is complex. However, we are working through this process and continue to carefully manage the supply to enable the potential re-opening of compassionate use at the earliest possible time and when continuous supply is available. The companies recognize the great unmet medical need for patients with metastatic melanoma and remain committed to the development of ipilimumab.
Regards,
Bristol-Myers Squibb
Something doesn't seem right here. There is something going on. A year to get your Protocol in place that was already in place.
It doesn't smell right!!!!
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I bet you it has something to do with the string of Pearls!!!!!!!!
Take Care,
Jimmy B
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Jimmy - I am interested in hearing your position on the Plexxikon/Roche drug Plx4032 that has made quite the headlines this week. Is it too early to get excited? To me, since they even state that this is not a cure, seems more like an palliative treatment for end stage cases. A sort of last resort treatment for those that qualify. Please provide your insight.
ReplyDeleteI find it curious that they follow up their announcement of the Avastin failure with Melanoma, which yielded $5 billion for last year with this new data on Plx4032. Just maybe it was timed in a way for them to soften the blow.
Mike Brockey
sMelanoma.com
Mike, To the Melanoma Patients that have this BRAF mutation, a 70% response rate is great news. While it is not a cure, it will prolong your live, and that may give enough time to find another therapy that works even better. My one question is will this therapy disqualify me from other therapies that I may wamt to pursue in the future.
ReplyDeleteAnother question is, will the Melanoma be able to mutate and find a way around this pathway. Will I have a reoccuence? Only time will tell.
Jimmy B