Phase I Study of Safety and Immunogenicity of ADU-623

PHASE1CompletedINTERVENTIONAL
Enrollment

11

Participants

Timeline

Start Date

January 8, 2014

Primary Completion Date

June 18, 2018

Study Completion Date

August 15, 2018

Conditions
Astrocytic TumorsGlioblastoma MultiformeAnaplastic AstrocytomaBrain Tumor
Interventions
BIOLOGICAL

Cohort 1

Four doses of IV ADU-623 at a dose of 3 x 10\^7cfu

BIOLOGICAL

Cohort 2

Four doses of IV ADU-623 at a dose of 3 x 10\^8cfu

BIOLOGICAL

Cohort 3

Four doses of IV ADU-623 at a dose of 3 x 10\^9cfu

DRUG

Antibiotics

A 3-day course of oral amoxicillin (500 mg three times per day) or trimethoprim/sulfamethoxazole in penicillin-allergic patients (160 mg trimethoprim / 800mg sulfamethoxazole at 12 hour intervals) will be initiated for each patient 3 days following each dose of ADU-623. Patients will receive a 7-day course of antibiotics starting at the end of treatment visit.

Trial Locations (1)

97213

Providence Cancer Center, Portland

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Aduro Biotech, Inc.

INDUSTRY

lead

Providence Health & Services

OTHER

NCT01967758 - Phase I Study of Safety and Immunogenicity of ADU-623 | Biotech Hunter | Biotech Hunter