Good stuff!
It's only a Phase 1 study, so dosing and safety will be the key focus. In itself, that's not likely to have a significant impact, as efficacy is the big brass ring. That will come later.
A fairly quick trial process, only 26 weeks from start to finish for the patient group. I shouldn't think it will be difficult to recruit Melanoma patients in Qld. Should see trial endpoint result by 4th Qtr 2016.
Ann: Prima unveils Phase I combination study of IMP321, page-4
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