drugset / Trial / NCT03491683

INO-5401 and INO-9012 Delivered by Electroporation (EP) in Combination With Cemiplimab (REGN2810) in Newly-Diagnosed Glioblastoma (GBM)

NCT03491683

Phase 1/2 Active not recruiting 52 enrolled Inovio Pharmaceuticals
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Phase 1/2 trial to evaluate safety, immunogenicity and preliminary efficacy of INO-5401 and INO-9012 in combination with cemiplimab (REGN2810), with radiation and chemotherapy, in subjects with newly-diagnosed glioblastoma (GBM).

Timeline

Start
2018-05-31
Primary completion
2026-12-31
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Cemiplimab Monoclonal antibody 350 mg Intravenous
Subject INO-5401 Other / unclassified 3 mg Intramuscular
Subject Rocakinogene Sifuplasmid Vaccine 1 mg Intramuscular
Background Temozolomide Small molecule 75 mg/m2

Indications