drugset / Trial / NCT04006119

Study of Ad-RTS-hIL-12 + Veledimex in Combination With Cemiplimab in Subjects With Recurrent or Progressive Glioblastoma

NCT04006119

Phase 2 Terminated 40 enrolled Alaunos Therapeutics
NaSingle-groupOpen-labelTreatment

Summary

This research study involves an investigational product: Ad-RTS-hIL-12 given with veledimex for production of human IL-12. IL-12 is a protein that can improve the body's natural response to disease by enhancing the ability of the immune system to kill tumor cells and may interfere with blood flow to the tumor. Cemiplimab-rwlc (Libtayo) is an antibody (a kind of human protein) that is being tested to see if it will allow the body's immune system to work against glioblastoma tumors. Libtayo (cemiplimab-rwlc) is currently FDA approved in the United States for metastatic cutaneous cell carcinoma (CSCC), but is not approved in glioblastoma. Cemiplimab-rwlc may help your immune system detect and attack cancer cells. Ad-RTS-hIL-12 and veledimex will be given in combination with cemiplimab-rwlc to enhance the IL-12 mediated effect observed to date. The main purpose of this study is to evaluate the safety and efficacy of a single tumoral injection of Ad-RTS-hIL-12 given with oral veledimex in combination with cemiplimab-rwlc.

Timeline

Start
2019-08-01
Primary completion
2021-08-05
Completion
2021-08-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Ad-RTS-hIL-12 Unknown 2e+11 unknown Other
Subject Cemiplimab Monoclonal antibody 350 mg Other
Subject veledimex Small molecule 20 mg Oral

Indications