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Glivec in Pediatric Chronic Myeloid Leukemia (CML)

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00845221
Enrollment
44
Registered
2009-02-18
Start date
2004-07-31
Completion date
Unknown
Last updated
2016-10-11

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

Conditions

Chronic Myeloid Leukemia

Brief summary

It is a phase 4 study, not randomised and multicentric. Within 2 months after the diagnosis, the patients daily receive imatinib by oral way during at least 1 year (260mg/m² once a day), i.e. until the cytogenetic analysis. Beyond 1 year of treatment, if a haematological relapse or a loss of the cytogenetic response is observed, the nature of the treatment suggested to the patient is left with the appreciation of the investigator. Later on, discontinuation of imatinib is discussed if a molecular remission (negative RT-PCR) is obtained and maintained for at least 2 years.

Interventions

DRUGImatinib mesylate 100 mg (Glivec)

260 mg/m2/day tablets

Sponsors

Poitiers University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
No

Inclusion criteria

* Old \< 18 years, male or female. * Chronic myeloid leukaemia confirmed on the cytogenetic level by the presence of the translocation t(9; 22) (q34; q11) or by the presence of transcript BCR-ABL in the event of absence of description of the translocation t(9; 22) (q34; q11). * Chronic phase of a chronic myeloid leukaemia * Absence of extra-medullary disease (except for a hepatomegaly and/or of a splenomegaly). * Absence of any former treatment of chronic myeloid leukaemia except for hydroxyurea. * Stop of hydroxyurea at least week before the beginning of the imatinib mesylate. * Diagnosis of chronic myeloid leukaemia in chronic phase recent (less than 2 months). * Score of Lansky ≥ 60. * Effective contraception among patients in age to procreate. * Written voluntary informed consent of the two parents or the legal guardian.

Exclusion criteria

* Patients with grade 3 / 4 cardiac disease. * Pathology cardiac, pulmonary, hepatic, renal or neurological of grade \> 2 (WHO). * Participation in a clinical trial in the 28 days preceding the beginning by the treatment. * Impossible Follow-up during at least 2 years, patient not compliant. * Expectant mother or nursing.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026