Neoepitope-based Personalized DNA Vaccine Approach in Pediatric Patients With Recurrent Brain Tumors

PHASE1RecruitingINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

October 2, 2024

Primary Completion Date

March 31, 2029

Study Completion Date

February 28, 2031

Conditions
Pediatric Recurrent Brain Tumor
Interventions
BIOLOGICAL

Personalized neoantigen DNA vaccine

At each vaccination time point, patients will receive one injection of the neoantigen DNA vaccine, one injection into the vastus lateralis.

DEVICE

Papivax Biotech TDS-IM v2.0

All study injections will be given intramuscularly using an integrated electroporation device (TDS-IM v2.0 device - Papivax Biotech).

PROCEDURE

Peripheral blood draw

-After trial enrollment and up to 7 days after the first vaccine dose (baseline); no more than 2 weeks after the 3rd vaccine dose; no more than 2 weeks after the 6th vaccine dose; two weeks after the last dose; time of progression or discontinuation (optional)

Trial Locations (1)

63110

RECRUITING

Washington University School of Medicine, St Louis

All Listed Sponsors
collaborator

Children's Discovery Institute

OTHER

lead

Washington University School of Medicine

OTHER