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Comparison of the therapeutic effect of FLANG chemotherapy regimen with FLANG plus cyclosporine in refractory or relapsed acute myeloid leukemia.

Comparison of the therapeutic effects of fludarabine-cytarabine-noventrone-granulocyte growth factor (FLANG) chemotherapy regimen with FLANG plus cyclosporine in patients with refractory or relapsed acute myeloid leukemia

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250605066068N1
Enrollment
20
Registered
2025-07-28
Start date
2025-06-28
Completion date
Unknown
Last updated
2025-08-19

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

Conditions

Condition 1: Refractory acute myeloid leukemia. Condition 2: relapsed acute myeloid leukemia. Acute myeloblastic leukemia, not having achieved remission Acute myeloblastic leukemia, in relapse

Interventions

Intervention 1: Intervention group: Patients with refractory or relapsed acute myeloid leukemia who receive Fludarabine 30mg/m2/day D1 to D5 IV - Cytarabine 2gr/m2/day D1 to D5 IV-Noantrone(mitoxantro

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1- Patients with refractory or relapsed acute myeloid leukemia in the age range of 15-60 years 2- Performance status based on Karnofsky criteria above 70 or ECOG = 1-2 EF (cardiac output) greater than 45 percent obtaining informed consent

Exclusion criteria

Exclusion criteria: 1- Occurrence of grade 3 or 4 drug toxicity 2- Heart, Respiratory, or Renal failure 3- Performance status based on Karnofsky criteria below 70 or ECOG =3

Design outcomes

Primary

MeasureTime frame
Achieving bone marrow remission. Timepoint: Two weeks after starting treatment. Method of measurement: Bone marrow aspiration and biopsy and pathologist report.;Drug Toxicity. Timepoint: one month. Method of measurement: Daily clinical examinations and use of checklist.;Cause of death. Timepoint: During hospitalization. Method of measurement: Reviewing patient's file documents.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmadreza Maghsoudi

Esfahan University of Medical Sciences

omid@mui.ac.ir+98 31 3235 0210

Outcome results

None listed

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