The NINLARO® (ixazomib) Regimen* Provides Durable Strength for Your Patients With Relapsed Multiple Myeloma Who May Benefit From Long-term Proteasome Inhibition1-3 

The first and only FDA-approved oral proteasome inhibitor-based regimen for patients with multiple myeloma at first relapse.1 The NINLARO regimen was studied in a broad range of patients and demonstrated a median PFS of 20.6 months vs 14.7 months with the Rd regimen*.

*The NINLARO regimen included NINLARO + lenalidomide + dexamethasone. The Rd regimen included placebo + lenalidomide + dexamethasone.1
Used herein to refer to treatment to disease progression or unacceptable toxicity.1
PFS=progression-free survival; PI=proteasome inhibitor.

The NINLARO regimen* is approved to treat multiple myeloma at first relapse1

NINLARO in combination with lenalidomide and dexamethasone is an approved treatment for relapsed multiple myeloma after at least 1 previous therapy, including indolent relapsed multiple myeloma. This combination is the only all-oral proteasome inhibitor-based regimen approved by the FDA for multiple myeloma treatment.

Category 1 NCCN Recommendation

Ixazomib (NINLARO) in combination with lenalidomide and dexamethasone is a National Comprehensive Cancer Network® (NCCN®) category 1 recommended treatment option for previously treated multiple myeloma.4

NINLARO patient profiles

Different patient types with relapsed multiple myeloma may benefit from the NINLARO triplet regimen.

NINLARO real-world studies

Real-world evidence can complement data from clinical trials.

NINLARO safety profile

The NINLARO regimen: a PI triplet with safety similar to the Rd regimen.

NINLARO dosing

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Find the dosing schedule for the NINLARO all-oral triplet regimen and information on dosage modifications.

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