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DARZALEX FASPRO®DARZALEX®
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APPROVED

DARZALEX FASPRO® + VRd is approved in transplant-ineligible patients with newly diagnosed multiple myelomaNDMM1

Prescribing
Information
DARZALEX FASPRO®DARZALEX®
This site is intended for US healthcare professionals.
Prescribing Information
DARZALEX FASPRO®DARZALEX®
Get in Touch
Dosing & Administration Guide
DARZALEX FASPRO®DARZALEX®
Support & Resources
Expert VideosMOAAdditional RegimensNCCN GuidelinesPractice SupportPatient Support & Resources
Get in Touch
FAQs
Patient Site
MM Portfolio
For APPs & Nurses
Go to DARZALEX® (daratumumab) & DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) HCP homepageGo to DARZALEX® (daratumumab) & DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) HCP homepage
DARZALEX FASPRO® monotherapy is the first and only FDA-approved treatment in high-risk smoldering multiple myeloma1DARZALEX FASPRO® monotherapy is now approved in high-risk smoldering multiple myeloma1
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Frontline DARZALEX®- and DARZALEX FASPRO®–Based Regimens Are Foundational
in Multiple Myeloma Treatment Approaches1,2

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Explore a
Triplet

Regimen with DARZALEX®

(daratumumab)

MAIA: DRd in Transplant-Ineligible NDMMExploratory Subgroup Analyses

Discover a
Quad

Regimen with DARZALEX FASPRO®

(daratumumab and hyaluronidase-fihj)

CEPHEUS: DVRd in Transplant-
Ineligible NDMM
PERSEUS: DVRd in Transplant-
Eligible NDMM

MAIA: Post hoc
 analyses of 

Treatment Duration

 with DARZALEX®+ Rd 

See Post Hoc Analyses

References:

  1. DARZALEX® [Prescribing Information]. Horsham, PA: Janssen Biotech, Inc.
  2. DARZALEX FASPRO® [Prescribing Information]. Horsham, PA: Janssen Biotech, Inc.