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manibiotech

07/03/25 9:08 PM

#774112 RE: GPha #774111

Yes the problem is they will need patient level data from external control arm also for FDA, not just the patients in compassionate use arm. 
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ATLnsider

07/03/25 9:11 PM

#774114 RE: GPha #774111

I agree GPha, I also believe that NWBio will be able to use RWD from treating other solid tumor cancers from Compassionate Use, Specials Program and Expanded Access.

This RWD could be used to help support label expansion beyond just treating malignant glioma patients, to include all or most solid tumor cancers.
Bullish
Bullish