Halozyme Announces Janssen Receives European Marketing Authorizations for DARZALEX® (daratumumab) Subcutaneous Formulation for Newly Diagnosed Systemic Light-chain Amyloidosis and Pre-Treated Multiple Myeloma

Jun 22, 2021

- Janssen received European approval for DARZALEX® (daratumumab) subcutaneous formulation in combination with bortezomib, cyclophosphamide and dexamethasone for the treatment of adult patients with newly diagnosed systemic light-chain (AL) amyloidosis, based on data from the Phase 3 ANDROMEDA study -

- Janssen also received approval for DARZALEX® SC in combination with pomalidomide and dexamethasone for adult patients with relapsed or refractory multiple myeloma, based on the Phase 3 APOLLO study -

PR Newswire

SAN DIEGO, June 22, 2021

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