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Zosuquidar in Combination With Daunorubicin and Cytarabine in Patients Ages 55-75 With Newly Diagnosed Acute Myeloid Leukemia (AML)

An Open-Label, Phase I/II, Multicenter Dose Escalation Study of Zosuquidar, Daunorubicin, and Cytarabine in Patients Ages 55-75 With Newly Diagnosed Acute Myeloid Leukemia

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00129168
Enrollment
100
Registered
2005-08-11
Start date
2005-08-31
Completion date
2008-03-31
Last updated
2008-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leukemia, Myeloid

Keywords

Leukemia, Myeloid, Relapse, Chemotherapy, Zosuquidar, Daunorubicin, Cytarabine, Acute, AML, Adult AML

Brief summary

Chemotherapy drugs use different ways to stop cancer cells from dividing so they stop growing or die. Zosuquidar may help daunorubicin and cytarabine kill more cancer cells by making cancer cells more sensitive to the drugs. It is not yet known whether daunorubicin and cytarabine are more effective with or without zosuquidar in treating acute myeloid leukemia.

Detailed description

Purpose: Phase I: To Evaluate the safety of different doses of zosuquidar. Phase II: This study is designed to study the safety and effectiveness of zosuquidar when given with daunorubicin and cytarabine in newly diagnosed AML patients.

Interventions

DRUGDaunorubicin
DRUGCytarabine

Sponsors

Kanisa Pharmaceuticals
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Newly diagnosed acute myeloid leukemia * Ages 55-75 years

Exclusion criteria

* Acute promyelocytic leukemia (FAB M3) * Patients must not have received prior chemotherapy for AML. * Prior exposure to anthracycline * Use of any investigational agent within 4 weeks prior to enrollment into the study For Phase II: * Patients must be P-glycoprotein positive

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026