Dose-escalation Study to Evaluate the Safety and Tolerability of GX-I7 in Patients With Glioblastoma

PHASE1CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

June 20, 2018

Primary Completion Date

September 25, 2020

Study Completion Date

September 25, 2020

Conditions
Newly Diagnosed Glioblastoma
Interventions
DRUG

GX-I7

During Treatment Period, patients will receive the assigned dose of GX-I7 intramuscular injection every 4\~12 weeks per cycle up to 6 cycles in the absence of unacceptable toxicity or clinically compelling evidence of disease progression.

Trial Locations (1)

06591

The Catholic University of Korea Seoul St. Mary's Hospital, Seoul

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Genexine, Inc.

INDUSTRY

NCT03619239 - Dose-escalation Study to Evaluate the Safety and Tolerability of GX-I7 in Patients With Glioblastoma | Biotech Hunter | Biotech Hunter