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

2014-07-23 22:00:34 | BioPortfolio

Summary

The purpose of this pilot safety study is to evaluate the safety and tolerability of JX-594 (Pexa-Vec) administered intravenously every 2 weeks in colorectal carcinoma patients who are refractory to or intolerant of oxaliplatin, irinotecan, and Erbitux treatments.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Carcinoma, Colorectal

Intervention

Recombinant Vaccinia GM-CSF; RAC VAC GM-CSF (JX-594)

Location

Samsung Medical Center
Seoul
Korea, Republic of

Status

Active, not recruiting

Source

Jennerex Biotherapeutics

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-23T22:00:34-0400

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