Clinical Trials Directory

Trials / Completed

CompletedNCT01564537

A Phase 3 Study Comparing Oral Ixazomib Plus Lenalidomide and Dexamethasone Versus Placebo Plus Lenalidomide and Dexamethasone in Adult Participants With Relapsed and/or Refractory Multiple Myeloma

A Phase 3, Randomized, Double-Blind, Multicenter Study Comparing Oral Ixazomib (MLN9708) Plus Lenalidomide and Dexamethasone Versus Placebo Plus Lenalidomide and Dexamethasone in Adult Patients With Relapsed and/or Refractory Multiple Myeloma

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
722 (actual)
Sponsor
Takeda · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether the addition of oral ixazomib to the background therapy of lenalidomide and dexamethasone improves progression free survival (PFS) in participants with relapsed and/or refractory multiple myeloma (RRMM).

Detailed description

The drug being tested in this study is called Ixazomib. Ixazomib is being tested to treat people who have relapsed and/or refractory multiple myeloma (RRMM). This study will look at progression free survival (PFS), overall survival (OS) and safety in participants who take ixazomib in addition to lenalidomide and dexamethasone compared to placebo in addition to lenalidomide and dexamethasone. The study enrolled 722 patients. Participants were randomly assigned (by chance, like flipping a coin) to one of the two treatment groups-which will remain undisclosed to the patient and study doctor during the study (unless there is an urgent medical need): * Ixazomib 4 mg + lenalidomide + dexamethasone * Placebo (dummy inactive pill) - this is a tablet that looks like the study drug but has no active ingredient + lenalidomide + dexamethasone All participants will receive treatment in 28 day cycles until disease progression or unacceptable toxicity. This multi-center trial will be conducted worldwide. The overall time to participate in this study is approximately 80 months. Participants will make multiple visits to the clinic, and will be contacted every 4 weeks for PFS and every 12 weeks for OS.

Conditions

Interventions

TypeNameDescription
DRUGIxazomibIxazomib capsules
DRUGLenalidomideLenalidomide capsules
DRUGDexamethasoneDexamethasone tablets
DRUGPlaceboIxazomib placebo-matching capsules

Timeline

Start date
2012-08-01
Primary completion
2014-10-01
Completion
2022-02-08
First posted
2012-03-28
Last updated
2023-03-10
Results posted
2016-01-27

Locations

24 sites across 2 countries: United States, Canada

Regulatory

Source: ClinicalTrials.gov record NCT01564537. Inclusion in this directory is not an endorsement.