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Clinical Trials/NCT02303522
NCT02303522
Completed
Not Applicable

A Retrospective Pooled Analysis of Complete Remission Among Pediatric Patients With Relapsed or Refractory B-cell Precursor Acute Lymphoblastic Leukemia (ALL)

Amgen1 site in 1 country207 target enrollmentDecember 9, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
B-cell Precursor Acute Lymphoblastic Leukemia (ALL)
Sponsor
Amgen
Enrollment
207
Locations
1
Primary Endpoint
Hematological Complete Remission (CR)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

An historical data comparator study for children with relapsed/refactory acute lymphoblastic leukemia (ALL).

Detailed Description

A retrospective observational study reviewing historical complete remission for pediatric patients who had either relapsed or refractory B-precursor acute lymphoblastic leukemia (ALL)

Registry
clinicaltrials.gov
Start Date
December 9, 2014
End Date
January 22, 2015
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Amgen
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Hematological Complete Remission (CR)

Time Frame: Approx. 1 year

To estimate hematological Complete Remission (CR) in pediatric patients with relapsed or refractory B-cell precursor Acute Lymphoblastic Leukemia (ALL)

Secondary Outcomes

  • Time to hematological CR(Approx. 1 year)
  • Overall survival(Approx. 1 year)
  • Molecular CR(Approx. 1 year)
  • Relapse Free Survival (RFS)(Approx. 1 year)
  • Receipt of HSCT after salvage treatment(Approx. 1 year)

Study Sites (1)

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