This phase 2 study was designed to assess the safety and efficacy of masitinib (AB1010) in patients with relapsing/refractory t(4;14) Multiple Myeloma. Response and progression were assessed according to the Bladé revised IMWG criteria1 from lowest point.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
24
masitinib 9 mg/kg/day per os
Hopital Saint Louis
Paris, France
Tumor Response Rate, based on the criteria published by Blade and on the criteria SWOG
Time frame: 16 weeks
Tumor response rate with AB1010 plus dexamethasone
Time frame: 16 weeks
Time to tumor progression and duration of response in responder patients
Time frame: 16 weeks
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