TOURMALINE-MM2: Oral Ixazomib-Rd vs Placebo-Rd for ASCT-Ineligible Patients With Newly Diagnosed MM

December 5-8, 2020; Online at https://www.hematology.org/meetings/annual-meeting
The addition of ixazomib to Rd was reasonably well tolerated and conferred a clinically meaningful, but not statistically significant 13.5-month improvement in PFS compared with the control arm.
Format: Microsoft PowerPoint (.ppt)
File Size: 391 KB
Released: December 9, 2020

Acknowledgements

Provided by Clinical Care Options, LLC

Clinical Care Options, LLC
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Sophia Kelley
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Supported by educational grants from
Amgen
AstraZeneca
Bristol-Myers Squibb
Epizyme Inc.
GlaxoSmithKline
Incyte Corporation
Janssen Biotech
Karyopharm Therapeutics Inc.
Novartis
PharmaEssentia Corp.
Seattle Genetics
Takeda Oncology

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