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Reduce the risk of disease progression by 37% Janssen CD38 antibody combination approved for second-line treatment of MM

 Last Update: 2021-08-02
 Source: Internet
 Author: User

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Janssen, a subsidiary of Johnson & Johnson, today announced that the U.

This approval is based on the results of a phase 3 clinical trial called APOLLO

In addition, the results of the study showed that Darzalex Faspro+Pd had a higher overall remission rate (69% vs.

Darzalex Faspro, jointly developed by Janssen and Genmab, is the first anti-CD38 antibody that can be administered by subcutaneous injection, reducing the time for patients to receive treatment from a few hours to a few minutes

Note: The original text has been deleted

Reference materials:

[1] Janssen Announces US FDA Approval of DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) in Combination with Pomalidomide and Dexamethasone for Patients with Multiple Myeloma After First or Subsequent Relapse.

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