Ipsen Phase Iii Napoli 3 Trial Of Onivyde Regimen Meets Primary Endpoint Demonstrating Statistically Significant Improvement In Os In Previously Untreated Mpdac
Ipsen phase III NAPOLI 3 trial of Onivyde regimen meets primary endpoint demonstrating statistically significant improvement in OS in previously untreated mPDAC
Ipsen announced the phase III NAPOLI 3 trial of Onivyde (irinotecan liposome injection) plus 5 fluorouracil/leucovorin and oxaliplatin (Nalirifox regimen) met its primary endpoint demonstrating clinically meaningful and statistically significant improvement in overall survival compared to nab-paclitaxel plus gemcitabine in 770 previously untreated patients with metastatic pancreatic ductal adenocarcinoma (mPDAC) and key secondary efficacy outcome of progression-free survival (PFS) also showed significant improvement over the comparator arm. The safety profile of Onivyde in the NAPOLI 3 trial was consistent with those observed in the previous phase I/II mPDAC study.
Ipsen intends to file a supplemental New Drug Application with the US Food and Drug Administration for Onivyde in combination with oxaliplatin plus 5- fluorouracil/leucovorin for the treatment of patients with previously untreated mPDAC following the Fast Track Designation granted in 2020. The clinical trial results will be presented at an upcoming medical conference.
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