drugset / Trial / NCT00175812

Differentiation Induction in Acute Myelogenous Leukemia

NCT00175812

Phase 1/2 Completed 24 enrolled University of Bergen
NaSingle-groupOpen-labelTreatment

Summary

Hypothesis: Differentiation induction therapy in acute myelogenous leukemia (AML) can be used to achieve disease control and stabilize peripheral blood counts in patients with acute myelogenous leukemia. Adult patients (\<18 years of age) who can be included: Elderly patients (\>60 years of age) with newly diagnosed AML who cannot achieve standard chemotherapy, patients with relapsed or resistant AML. Patients with relapsed or resistant AML who cannot receive intensive chemotherapy. Treatment: Patients will be treated with all-trans retinoic acid (oral administration), valproic acid (7 days intravenous administration and later oral administration)and theophyllamine (7 days intravenous administration and later oral administration). Duration of treatment at least 2 months or until disease progression. Maximal duration of treatment 2 years. Followup: Clinical evaluation, peripheral blood samples, bone marrow samples.

Timeline

Start
2004-11
Primary completion
2008-05
Completion
2009-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Theophylline Small molecule Intravenous
Subject Tretinoin Small molecule 22.5 mg/m2 Oral
Subject Valproic Acid Small molecule Intravenous