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Re: To infinity and beyond! post# 144438

Wednesday, 04/06/2016 1:44:01 PM

Wednesday, April 06, 2016 1:44:01 PM

Post# of 403091
In case you forgot, here are the secondary endpoints of the Prurisol trial:

Secondary Outcome Measures:
-The Secondary efficacy endpoints are the percentage of subjects in each treatment group with:≥ 2 point improvement in IGA at 28 days [ Time Frame: 28 days ] [ Designated as safety issue: No ]
-The Secondary efficacy endpoints are the percentage of subjects in each treatment group with: ≥ 2 point improvement in IGA at 56 days [ Time Frame: 56 Days ] [ Designated as safety issue: No ]
-The Secondary efficacy endpoints are the percentage of subjects in each treatment group with: ≥1 point improvement in Scaling Score of Target Lesion at 28 days [ Time Frame: 28 Days ] [ Designated as safety issue: No ]
-The Secondary efficacy endpoints are the percentage of subjects in each treatment group with: ≥1 point improvement in Scaling Score of Target Lesion at 56 days [ Time Frame: 56 Days ] [ Designated as safety issue: No ]
-The Secondary efficacy endpoints are the percentage of subjects in each treatment group with: ≥1 point improvement in Scaling Score of Target Lesion at 84 days [ Time Frame: 84 Days ] [ Designated as safety issue: No ]

https://clinicaltrials.gov/ct2/show/NCT02494479?term=cellceutix&rank=2



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