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A Prospective Trial Evaluating the Safety of a Shortened Infusion of Ramucirumab in Patients with Gastrointestinal Cancer
Advertisement Advertisement Naoya Hashimotoa, Seiichiro Mitanib, Hiroya Taniguchi (h.taniguchi{at}aichi-cc.jp)*,b, Yukiya Naritab, Kyoko Katob, Toshiki Masuishib, Shigenori Kadowakib, Sachiyo Onishic, Masahiro Tajikac, Shinji Takahashia, Kazuhiro Shimomuraa, Chihoko Takahatad, Eri Hottad, Makiko Kobarad and Kei Murob a Department of Pharmacy, Aichi Cancer Center Hospital, Nagoya, Japan b Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan c Department of Endoscopy,...
A Prospective Trial Evaluating the Safety of a Shortened Infusion of Ramucirumab in Patients with Gastrointestinal Cancer
Ramucirumab is usually administered over 60 minutes, during which it is unlikely to cause infusion‐related reactions (IRRs). This prospective study evaluated the safety of a shortened infusion of ramucirumab. Patients who received their first dose of ramucirumab in a 60‐minute infusion without developing IRRs were eligible and received their second ramucirumab dose for 20 minutes.
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