drugset / Trial / NCT02795988

A Study of IMU-131(HER-Vaxx) and Chemotherapy Compared to Chemotherapy Only in Patients With HER2 Positive Advanced Gastric Cancer

NCT02795988

Phase 1/2 Completed 64 enrolled Imugene Limited
RandomizedParallel-groupSingle-blindTreatment

Summary

The Phase 1b study is an open-label, multicenter dose escalation study designed to assess the safety, tolerability, immunogenicity and recommended phase 2 dose (RP2D) of IMU-131. The RP2D will be evaluated in the dose expansion Phase 2 study. The Phase 2 study is a randomized, open label comparison of IMU-131 plus standard of care chemotherapy versus standard of care chemotherapy alone.

Timeline

Start
2017-08-30
Primary completion
2024-03-20
Completion
2024-03-20

Drugs

EvaluationDrugModalityDoseRoute
Subject IMU-131 Vaccine 10 ug
Subject IMU-131 Vaccine 30 ug
Subject IMU-131 Vaccine 50 ug
Background Capecitabine Small molecule 1000 mg/m2 Oral
Background Cisplatin Other / unclassified 80 mg/m2 Intravenous
Background Oxaliplatin Small molecule 130 mg/m2 Intravenous
Background fluorouracil Small molecule 4000 mg/m2 Other