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A Phase II Study of Delayed Local Treatment for High Risk Neuroblastoma

Phase 2
Conditions
High Risk Neuroblastoma
Registration Number
JPRN-UMIN000005045
Lead Sponsor
Japan Neuroblastoma Study Group
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
75
Inclusion Criteria

Not provided

Exclusion Criteria

Active double cancer; pregnant or possibly pregnant women and those during breast feeding; patients with psychological disease or symptoms who have difficulty in receiving protocol treatment; patients with disease that may interfere with the protocol treatment

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
3-year progression-free survival rate
Secondary Outcome Measures
NameTimeMethod
3-year overall survival rate, the incidence of adverse events, clinical response rate before surgery
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