› Forums › General Melanoma Community › FDA priority review for nivolumab
- This topic has 6 replies, 2 voices, and was last updated 11 years, 2 months ago by
mary1233.
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- September 27, 2014 at 2:43 am
As expected, the FDA today committed to a six-month priority review with BMS for nivolumab ("Opdivo"), following a similar process as that done with Merck for pembrolizumab ("Keytruda"):
http://www.reuters.com/article/2014/09/26/us-bristol-myers-fda-idUSKCN0HL2EH20140926
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- September 27, 2014 at 3:15 pm
Thanks, hopefully it will be approved as a first line treatment withut too many restrictions.
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- September 27, 2014 at 3:15 pm
Thanks, hopefully it will be approved as a first line treatment withut too many restrictions.
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- September 27, 2014 at 3:15 pm
Thanks, hopefully it will be approved as a first line treatment withut too many restrictions.
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- September 28, 2014 at 4:56 pm
I hope that they do not require people to fail with ipi the way they did with the merck drug. The rate of success with ipi is fairly low, and yet with Keytruda the FDA requires that huge expense before the next huge expense. I do not understand our medical system.
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- September 28, 2014 at 4:56 pm
I hope that they do not require people to fail with ipi the way they did with the merck drug. The rate of success with ipi is fairly low, and yet with Keytruda the FDA requires that huge expense before the next huge expense. I do not understand our medical system.
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- September 28, 2014 at 4:56 pm
I hope that they do not require people to fail with ipi the way they did with the merck drug. The rate of success with ipi is fairly low, and yet with Keytruda the FDA requires that huge expense before the next huge expense. I do not understand our medical system.
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