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XBiotech Says The Primary Endpoint For The Phase 2 Study Was To Assess The Safety And Tolerability Of Natrunix When Used With The ON+5FU+LV Combination, There Were Fewer Adverse Events Of Any Kind During The 24-Week Treatment Period For The Natrunix...

XBiotech Says The Primary Endpoint For The Phase 2 Study Was To Assess The Safety And Tolerability Of Natrunix When Used With The ON+5FU+LV Combination, There Were Fewer Adverse Events Of Any Kind During The 24-Week Treatment Period For The Natrunix...

Xbiotech表示,第2期研究的主要終點是評估當Natrunix與ON+5FU+LV組合使用時的安全性和耐受性,在24周的治療期間,Natrunix的任何種類的不良事件更少。
Benzinga ·  06/18 11:49

XBiotech Says The Primary Endpoint For The Phase 2 Study Was To Assess The Safety And Tolerability Of Natrunix When Used With The ON+5FU+LV Combination, There Were Fewer Adverse Events Of Any Kind During The 24-Week Treatment Period For The Natrunix Arm Compared To Placebo, With Markedly Fewer Events In Specific Categories Of Adverse Events During That Time

xBiotech表示,2期研究的主要終點是評估Natrunix的安全性和耐受性,當與ON+5FU+LV組合使用時,與安慰劑相比,Natrunix組在24周治療期內發生的任何不良事件都更少,在此期間,特定類別的不良事件明顯減少

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