Blood
US FDA approves J&J’s blood cancer therapy
10
Aug
Aug
Aug 10 (Reuters) – Johnson & Johnson (JNJ.N) said on Thursday the U.S. Food and Drug Administration had approved its antibody-based therapy for patients with a difficult-to-treat type of blood cancer.
The therapy, talquetamab-tgvs branded as Talvey, belongs to a class called bispecific antibodies designed to bring a cancer cell and an immune cell together so the body’s immune system can kill the cancer.
Talvey was approved as a weekly or biweekly subcutaneous, or under-the-skin, injection, the company said.
Reporting by Mariam Sunny in Bengaluru; Editing by Krishna Chandra Eluri
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