drugset / Trial / NCT02323230

A Study of DPX-Survivac Vaccine Therapy in Patients With Recurrent Survivin-expressing DLBCL

NCT02323230

Phase 2 Terminated 4 enrolled ImmunoVaccine Technologies, Inc. (IMV Inc.)
NaSingle-groupOpen-labelTreatment

Summary

This phase 2 study was designed to assess the efficacy and safety of DPX-Survivac plus low dose cyclophosphamide in up to 24 subjects with recurrent diffuse large B-cell lymphoma (DLBCL) who are not eligible for transplant. However, with the evolving field of immunotherapy Immunovaccine has begun to focus on combination therapies, combining DPX-Survivac treatment with checkpoint inhibitors and other immune modulators. This phase 2 study was therefore terminated with fewer subjects than planned to allow the progress of other studies, such as NCT03349450.

Timeline

Start
2015-01
Primary completion
2017-06
Completion
2018-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified Oral
Subject maveropepimut-S Vaccine Subcutaneous