Looks like pretty impressive interim data to me
new positive data for DEP® irinotecan in the platinum-resistant ovarian cancer patient cohort, where the objective response rate (ORR2) in patients dosed every 2 weeks (Q2W) has increased from the previously reported 29% to 43%. In addition to this impressive efficacy, the duration of responses to DEP® irinotecan treatment in these heavily pre-treated ovarian cancer patients, with tumour shrinkage of up to 60%, now have durations of up to 45 weeks, compared with 36 weeks reported previously
DEP® irinotecan’s impressive ORR of 43% in these heavily pre-treated patients compares very favourably to standard-of-care single-agent therapies for platinum-resistant ovarian cancer, including paclitaxel (Taxol®), topotecan (Hycamtin®), gemcitabine (Gemzar®) or pegylated liposomal doxorubicin (Caelyx®), which report ORRs ranging from ~9 to 16%
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- Ann: DEP irinotecan clinical data presented at AACR meeting
Ann: DEP irinotecan clinical data presented at AACR meeting, page-9
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