drugset / Trial / NCT01051063

Evaluation of a New Anti-cancer Immunotherapy in Adult Acute Myeloid Leukemia Patients With a Suboptimal Clinical Response to Induction Chemotherapy

NCT01051063 ↗

Phase 1 Completed 17 enrolled GlaxoSmithKline
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the clinical activity and safety of a WT1 Antigen-Specific Cancer Immunotherapeutic (WT1 ASCI) as post-induction therapy in adult patients with WT1-positive AML presenting a suboptimal clinical response to induction chemotherapy. The study will also assess whether this treatment induces a specific immune response to the malignancy.

Timeline

Start
2009-12-09
Primary completion
2016-04-26
Completion
2016-04-26

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK2130579A Other / unclassified — Intramuscular