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Phase II study to evaluate the safety and the efficacy of CBD (Bortezomib, Cyclophosphamide, Dexamethasone) regimen for the patients with relapsed and/or refractory multiple myeloma

Phase 2
Recruiting
Conditions
relapsed and/or refractory multiple myeloma
Registration Number
JPRN-UMIN000003076
Lead Sponsor
ara Hospital Kinki University School Of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

performance status:3 and 4(excluding PS3 by bone pain and fracture)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
safety (neurotoxixty evaluated by FACT/GOG NTX ver. 4.0)
Secondary Outcome Measures
NameTimeMethod
response rate as efficacy (antitumor activity) time to response, response rate after 5 more cycles, progression free survival, overall survival
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