Recombinant Vaccinia Virus Administered Intravenously in Patients With Metastatic, Refractory Colorectal Carcinoma

第1/2相 完了 NCT01394939

概要

The purpose of this study is to evaluate the safety, tolerability, and efficacy of JX-594 (Pexa-Vec) administered intravenously either alone or in combination with Irinotecan in colorectal carcinoma patients who are refractory to or intolerant to standard therapy.

Determine Radiographic Response Rate of Patients Enrolled in the Phase 2a Portion of the Study

Scans every 8 weeks until progression, assessed up to 25 months · Participants

BENITIONS で見る ClinicalTrials.gov の原文を見る

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すべての治験