Revlimid
For healthcare professionals only.
In R/R MM* patients who have previously
received REVLIMID and bortezomib, did you
know you can achieve an overall
survival benefit without
changing classes?

View data now

For healthcare professionals only.

X
Beam Revlimid

In R/R MM* patients who have received REVLIMID and bortezomib

Proven OS benefit vs

high-dose dex1†

Reduced risk of death
vs high-dose dex

MM=multiple myeloma; R/R=relapsed/refractory.

A Foundation of Therapy in MM2,3

IMNOVID in combination with dexamethasone is indicated in the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least 2 prior treatment regimens, including both lenalidomide and bortezomib, and have demonstrated disease progression on the last therapy.2

Patients received a median of 5 lines of prior therapy. At 15.4 month follow-up, IMNOVID + dex median OS was 13.1 months vs 8.1 months with high-dose dex (HR 0.72; P=0.009) (ITT population, N=455).

*
†
28%

11/18  INT-POMA180001

EU Summary of Product Characteristics
References
X

References: 1. Dimopoulos MA, Weisel KC, Song KW, et al. Haematologica. 2015;100:1327-1333. 2. IMNOVID [Summary of Product Characteristics]. Utrecht, Netherlands, Celgene Europe B.V.; 2018. 3. Larocca A, Mina R, Gay F, Bringhen S, Boccadoro M. Oncotarget. 2017;8:60656-60672.