› Forums › General Melanoma Community › Adjuvant Tx Stage III-IV
- This topic has 6 replies, 2 voices, and was last updated 12 years, 1 month ago by
SBeattie.
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- October 31, 2013 at 7:17 pm
Just wondering if anyone has any idea re: if/when PD-1 and combo with ipi is FDA approved, it will be indicated for Stage III and IV 'resected' patients? I elected to watch/wait (the latter category) instead of enroll in the ipi 3mg or interferon trial, fearful of getting interferon (I know, if one doesn't try, then one will NEVER know) and fear of messing up getting into ipi-PD-1 trial if…more likely when, I may need it…unsights?
Thank you all…
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- October 31, 2013 at 7:22 pm
Your best bet would be to look at the current Phase III clinical trials for the drug or combo. If they are doing phase III clinical trials for adjuvant therapy, the drugs will probably be approved for such (that is if trials show benefit in an adjuvant setting). But if all the trials are for people with active disease, it's more likely that the drug will have the same constraints when it is approved. The trials are a pretty good indication of after market approval.
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- October 31, 2013 at 7:22 pm
Your best bet would be to look at the current Phase III clinical trials for the drug or combo. If they are doing phase III clinical trials for adjuvant therapy, the drugs will probably be approved for such (that is if trials show benefit in an adjuvant setting). But if all the trials are for people with active disease, it's more likely that the drug will have the same constraints when it is approved. The trials are a pretty good indication of after market approval.
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- October 31, 2013 at 7:22 pm
Your best bet would be to look at the current Phase III clinical trials for the drug or combo. If they are doing phase III clinical trials for adjuvant therapy, the drugs will probably be approved for such (that is if trials show benefit in an adjuvant setting). But if all the trials are for people with active disease, it's more likely that the drug will have the same constraints when it is approved. The trials are a pretty good indication of after market approval.
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