BENITIONSClinical Trial Intelligence

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

Phase 1/2 Completed NCT01394939

ConditionColorectal Carcinoma, CRC
PhasePhase 1/2
SponsorJennerex Biotherapeutics
StatusCompleted
Enrollment52 participants
InterventionsJX-594, Irinotecan
Start dateJan, 2012
Completion dateJun, 2015
Results postedJan 8, 2021

Summary

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

Single Agent_ Cohort 10 Participants
Single Agent_Cohort 20 Participants
Combination_Cohort 30 Participants
Combination_Cohort 41 Participants
Single Agent_ Cohort 10 Participants
Single Agent_Cohort 20 Participants

Open in BENITIONS View on ClinicalTrials.gov

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