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Evaluation of the Effect of deferasirox on the treatment of ??Acute myeloid leukemia

a pilot study to Assess the therapeutics indicators in Patients With Acute Myeloid Leukemia Undergoing therapy With deferasirox in Afzalipour Hospital of Kerman

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200313046756N2
Enrollment
40
Registered
2021-05-08
Start date
2022-09-23
Completion date
Unknown
Last updated
2022-08-29

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

Conditions

Acute myeloblastic leukemia. Acute myeloblastic leukemia

Interventions

Intervention 1: Intervention group: receive the standard treatment Cytarabine and idarubicin (7+3) with oral intake of Deferasirox capsule 360 mg daily for 28 days. Intervention 2: Control group: rece

Sponsors

Kerman University of Medical Sciences
Lead Sponsor
Nano Fanavaran Alvand pharmaceutical co.
Collaborator
AryaTinaGene biopharmaceutical co.
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age between 18-65 years AML/non-APL

Exclusion criteria

Exclusion criteria: HIV infected patients or Hepatitis B,C patients Patients with AML-induced neurological involvement Patients with uncontrolled blood pressure and heart failure Patients with a history of ocular toxicity due to iron chelators drugs

Design outcomes

Primary

MeasureTime frame
The number of white blood cells. Timepoint: on days 14 and 28. Method of measurement: Test for complete blood cell count.;Number of red blood cells. Timepoint: on days 14 and 28. Method of measurement: Test for complete blood cell count.;Platelet numbers. Timepoint: on days 14 and 28. Method of measurement: Test for complete blood cell count.;Percentage of CD34 + leukemia blasts of bone marrow biopsy specimen. Timepoint: on days 14 and 28. Method of measurement: Flow cytometry with CD34 monoclonal antibody.

Secondary

MeasureTime frame
Reactive oxygen species rate in +CD34 leukemic blasts bone marrow biopsy sample. Timepoint: on days 14 and 28. Method of measurement: Flow cytometry.;The rate of apoptotic cells in +CD34 leukemic blasts bone marrow biopsy sample. Timepoint: on days 14 and 28. Method of measurement: Flow cytometry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAliasghar Tirgar

Kerman University of Medical Sciences

a.tirgar@kmu.ac.ir0098342462413

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026