Multiple Myeloma Clinical Trial
Official title:
An Open-Label, Dose-Escalation, Phase 1/2 Study of the Oral Formulation of IXAZOMIB (MLN9708), Administered Twice-weekly in Combination With Lenalidomide and Dexamethasone in Patients With Newly Diagnosed Multiple Myeloma Requiring Systemic Treatment
The purpose of this study is to determine the safety, tolerability, maximum tolerated dose (MTD), and recommended phase 2 dose (RP2D) in phase 1 and to determine the combined response rate of clinical response CR and very good partial response (VGPR) in phase 2 of oral (PO) ixazomib administered twice-weekly in combination with lenalidomide and low-dose dexamethasone in a 21-day cycle in participants with newly diagnosed multiple myeloma (NDDM).
The drug being tested in this study is called ixazomib. Ixazomib was tested to slow disease
progression and improve overall survival in participants who have newly diagnosed multiple
myeloma (NDMM). This study looked at the safety, tolerability and response in participants
when administered in combination with lenalidomide and low-dose dexamethasone.
The study enrolled 64 patients. Participants were assigned to one of the 3 treatment groups:
- Phase 1 Ixazomib 3 mg
- Phase 1 Ixazomib 3.7 mg
- Phase 2 Ixazomib 3 mg
All participants were administered with Ixazomib capsules, orally, twice-weekly on Days 1, 4,
8, and 11 along with lenalidomide capsules, orally, once daily on Days 1-14 and
dexamethasone, capsules, orally, once daily on Days 1, 2, 4, 5, 8, 9, 11, and 12 for up to 16
cycles in the absence of disease progression or unacceptable toxicity as induction therapy
during Phase 1. Participants with stable or responding disease continued receiving ixazomib
capsules, orally, twice weekly on Days 1, 4, 8, and 11 in 21-day treatment cycles as
maintenance therapy until progressive disease or unacceptable toxicity.
This multi-center trial conducted in the United States. The overall time to participate in
this study was 2037 days. Participants will make multiple visits to the clinic, and a final
visit after 30 days after last dose of study drug for a follow-up assessment.
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