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Clinical Trials/EUCTR2010-022235-10-IT
EUCTR2010-022235-10-IT
Active, not recruiting
Not Applicable

A Phase I/II study of Azacitidine (Vidaza®) in pediatric patients with newly diagnosed or relapsed high-grade pediatric MDS or JMML - Azacitidine in high grade MDS and JMML pediatric patients

Erasmus MC0 sites65 target enrollmentFebruary 6, 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Advanced Myelodysplastic Syndromes (MDS) and Juvenile Myelomonocytic Leukemia (JMML)
Sponsor
Erasmus MC
Enrollment
65
Status
Active, not recruiting
Last Updated
12 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
February 6, 2013
End Date
TBD
Last Updated
12 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Erasmus MC

Eligibility Criteria

Inclusion Criteria

  • In this study 4 subgroups of patients are eligible, which will be enrolled in 4 different strata:
  • stratum 1: newly diagnosed patients with advanced MDS (RAEB or RAEB\-t) in a ‘pre stem cell transplantation window’.
  • stratum 2: relapsed patients with advanced MDS in a ‘re\-transplantation window’. At relapse azacitidine may also be continued when a 2nd transplant is not feasible, as long as the patient benefits from treatment.
  • stratum 3: newly diagnosed patients with JMML in a ‘pre\-stem cell transplantation window’.
  • stratum 4: relapsed patients with JMML in a ‘re\-transplantation window’. Azacitidine may also be continued when a 2nd transplant is not feasible and as long as the patient benefits from treatment.
  • straum 5:newly diagnosed or relapsed patients with secondary advanced MDS, occurring after
  • chemotherapy, radiotherapy and or stem\-cell transplantation, or secondary cases after
  • prior treatment for aplastic anemia. Note: secondary MDS cases after bone\-marrow failures or familial cases are not eligible
  • General conditions:
  • Advanced primary or secondary MDS or JMML confirmed by the diagnostic criteria as specified in the EWOG\-MDS 2006 protocol (see appendix 1\)

Exclusion Criteria

  • Prior or current history:
  • Other serious illnesses or medical conditions
  • Genetic abnormalities indicative of AML
  • JMML patients in whom a diagnosis of Noonan syndrome is suspected based on clinical history and/or presenting symptoms
  • Patients with secondary MDS with underlying bone\-marrow failure syndromes or with familial MDS
  • Isolated extramedullary disease
  • Symptomatic CNS\-involvement
  • Current uncontrolled infection
  • Cardiac toxicity (shortening fraction below 28%)
  • Concurrent treatment with any other anti\-cancer therapy is not allowed

Outcomes

Primary Outcomes

Not specified

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