MedPath

A Phase I Study of IGN523 in Subjects With Relapsed or Refractory AML

Phase 1
Completed
Conditions
Acute Myelogenous Leukemia
Acute Myeloid Leukemia
Interventions
Registration Number
NCT02040506
Lead Sponsor
Igenica Biotherapeutics, Inc.
Brief Summary

This study will examine the safety and tolerability of IGN523 administered as an IV infusion. The main purpose of the study is to determine the maximum tolerated dose (MTD), which is the highest dose that does not cause unacceptable side effects of IGN523 in patients with acute myeloid leukemia (AML). The MTD will be determined by observing the dose-limiting toxicities (the side effects that prevent further increases in dose) of IGN523. In addition, the pharmacokinetic profile and anti-leukemia activity of IGN523 will be assessed. A recommended Phase 2 dose (RP2D) of IGN523 will be identified, on the basis of safety, pharmacokinetic (PK), and pharmacodynamic (PD) data.

Detailed Description

Primary Objectives:

* Evaluate the safety and tolerability of IGN523 administered weekly

* Determine the MTD and dose limiting toxicity (DLT) of IGN523 when administered weekly during the DLT Evaluation Period

* Identify a recommended Phase 2 dose (RP2D) of IGN523 on the basis of safety, PK, and PD data

Secondary Objectives:

* Assess the incidence of antibody formation to IGN523

* Characterize the PK of IGN523 in subjects with relapsed or refractory AML

* Perform a preliminary assessment of the anti-leukemic activity of IGN523 in subjects with relapsed or refractory AML

* Perform a preliminary assessment of biologic markers that might predict IGN523 anti-leukemic activity

Estimated Enrollment: 50 Study Start Date: February 2014 Estimated Study Completion Date: March 2016 Estimated Primary Completion Date: September 2015 (Final data collection for primary outcome measure)

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
19
Inclusion Criteria
  • Relapsed or treatment-refractory AML
  • Eastern Cooperative Oncology Group status 0-2
  • Life expectancy of at least 12 weeks
  • Adequate baseline renal and hepatic function
  • Measurable disease (eg, peripheral blasts greater than 5%)
Exclusion Criteria
  • Chronic myelogenous leukemia in blast crisis
  • Monoclonal therapy within 4 weeks, or chemotherapy or radiotherapy within 2 weeks
  • Unresolved acute toxicity from prior anti-cancer therapy
  • Prior allogeneic stem cell transplant and active graft-versus-host disease requiring systemic immunosuppressive therapy within 15 days prior to screening
  • History of severe allergic or anaphylactic reactions to monoclonal antibody therapy
  • Known current leptomeningeal or central nervous system (CNS) involvement of leukemia

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
IGN523IGN523IGN523
Primary Outcome Measures
NameTimeMethod
Incidence of adverse eventsThrough 1 month following last dose
Secondary Outcome Measures
NameTimeMethod
Blood concentrations of IGN523Through 6 months following last dose
Incidence of antidrug antibodies to IGN523Through 6 months following last dose
Assess anti-leukemic activity of IGN523Initial assessment after 8 weeks of treatment

Subjects with measurable disease will be assessed by standard criteria (Cheson). Subjects will be formally evaluated for response at the end of Cycle 2; additional evaluations may be performed during the study as clinical indicated.

Trial Locations

Locations (6)

UCSD Medical Center / Thornton Hospital

🇺🇸

La Jolla, California, United States

Indiana Blood and Marrow Transplantation Clinic

🇺🇸

Indianapolis, Indiana, United States

MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

University of Michigan Health System

🇺🇸

Ann Arbor, Michigan, United States

University of Washington

🇺🇸

Seattle, Washington, United States

Winship Cancer Institute, Emory University

🇺🇸

Atlanta, Georgia, United States

© Copyright 2025. All Rights Reserved by MedPath