Phase I Study to Evaluate the Safety and Efficacy of Telomelysin (OBP-301) in Patients With Hepatocellular Carcinoma

PHASE1UnknownINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

October 31, 2014

Primary Completion Date

April 30, 2019

Study Completion Date

April 30, 2021

Conditions
Carcinoma, Hepatocellular
Interventions
BIOLOGICAL

OBP-301

A range of dose levels is investigated and the starting dose is 1x1010 VP/tumor. Dose administration will be conducted through a dose-escalating scheme from 1x1010 VP/tumor to 1x1011 VP/tumor, 1x1012 VP/tumor, 3x1011 VP/tumor and 3x1012 VP/tumor.

Trial Locations (2)

10002

RECRUITING

National Taiwan University Hospital, Taipei

602-739

RECRUITING

Pusan National University Hospital, Busan

Sponsors
All Listed Sponsors
collaborator

Medigen Biotechnology Corporation

INDUSTRY

lead

Oncolys BioPharma Inc

INDUSTRY