A Study of Active Immunotherapy With GRNVAC1 in Patients With Acute Myelogenous Leukemia (AML)

Asterias Biotherapeutics, Inc.21 enrolled

Overview

This is a phase II study to evaluate the safety, feasibility and efficacy of immunotherapy with GRNVAC1 in patients with AML.

This is a multicenter, open-label evaluation of feasibility, safety and immunotherapy in patients with AML in complete clinical remission. Patients will undergo leukapheresis prior to or shortly after completing consolidation chemotherapy. Dendritic cells will be transfected with the messenger RNA encoding human telomerase reverse transcriptase (hTERT) and a portion of the lysosome-associated membrane protein LAMP-1 (LAMP), matured, aliquoted, and cryopreserved. The final autologous vaccine product is referred to as GRNVAC1. Patients will be vaccinated with weekly for 6 weeks,will "rest" for 4 weeks, then will receive 6 boost injections, each administered every other week for 12 weeks. Patients will be followed every 4 weeks until Week 54, then every 3 months for 1 year, then every 6 months up to approximately 5 years from the first vaccination or until relapse/progression.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Acute Myelogenous Leukemia

Interventions

GRNVAC1BIOLOGICAL

Autologous dendritic cell vaccine

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * AML in first complete remission (CR1) or in second complete remission (CR2) with CR1 \>/= 6 months * Has completed at least one cycle of consolidation chemotherapy within past 6 months * Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 * Adequate hepatic/renal function Exclusion Criteria: * CR1 and good risk cytogenetic features \[t(15;17), t(8;21), inv(16) or t(16:16)\] * Central nervous system or leptomeningeal disease * Allogeneic stem cell transplant planned or expected * Documented allergy to penicillin or beta-lactam antibiotics * Active or ongoing autoimmune disease * Clinically significant pulmonary or cardiovascular disease

Locations (6)

Emory University School of Medicine

Atlanta, Georgia, United States

Loyola University Medical Center

Maywood, Illinois, United States

Washington University School of Medicine, Siteman Cancer Center

St Louis, Missouri, United States

University of Nebraska Medical Center

Omaha, Nebraska, United States

Outcomes

Primary Outcomes

Feasibility will be assessed by examining whether enough cells are collected during leukapheresis, whether enough vaccine is manufactured for at least 2 injections, and whether the patient is still in remission when the vaccine is released.

Time frame: 1 year

Secondary Outcomes

Immunological response, defined as the proportion of patients with a positive induction of hTERT-specific T cells to twice the pre-vaccination level, the proportion of patients with DTH, and event-free survival.

Time frame: 2 years

Data from ClinicalTrials.gov

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