Idarubicin
DrugChemotherapy
NCT Number: NCT02835729
The purpose of this study is to characterize the regimen limiting toxicities (RLT) and recommended Phase 2 dose (RP2D) of indoximod in patients with newly diagnosed AML receiving remission induction chemotherapy with cytarabine and idarubicin.
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Notify Me18 year and older
All sexes
Interventional
Phase 1
Augusta University, Augusta, Georgia, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Chemotherapy
Chemotherapy
IDO pathway inhibitor
IDO pathway inhibitor
IDO pathway inhibitor
Time frame: 6 months
Phase 1
Time frame: 6 months
Phase 1
Time frame: 2 years
Time frame: 2 years
Time frame: 2 years
Time frame: 2 years
Time on study to induction failure, relapse or death
Time frame: 2 years
Time frame: 2 years
Time frame: 2 years
Time frame: 2 years
Time frame: 6 months
Characterize the pharmacokinetics (PK) of indoximod, idarubicin and cytarabine through analysis of blood samples
Time frame: 2 years
Characterize the pharmacodynamic (PD) effect of indoximod
Time frame: 2 years
Time frame: 2 years
Time frame: 2 years
NewLink Genetics Corporation
Industry
A Phase 1 Trial of Indoximod in Combination With Idarubicin and Cytarabine in Patients With Newly Diagnosed Acute Myeloid Leukemia (AML)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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