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Halozyme, JNJ Win FDA Approval For DARZALEX Faspro In High-Risk Smoldering Multiple Myeloma

By RTTNews Staff Writer   ✉   | Published:   | Follow Us On Google News

Halozyme Therapeutics, Inc. (HALO), Friday announced that Johnson & Johnson has received U.S. Food and Drug Administration approval of a new indication for DARZALEX Faspro as a single agent treatment of adult patients with high-risk smoldering multiple myeloma.

The approval is based on the findings from the AQUILA study, which evaluated the efficacy and safety of DARZALEX Faspro.

Co-formulated with the company's drug delivery technology ENHANZE, Halozyme expects the approval to further strengthen DARZALEX Faspro's role as a cornerstone therapy across all stages of multiple myeloma.

Currently, HALO is trading at $68.65, up 0.38 percent on the Nasdaq.

For comments and feedback contact: editorial@rttnews.com

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