Johnson & Johnson has announced positive topline results from the investigational Phase 3 MajesTEC-9 study evaluating TECVAYLI® (teclistamab-cqyv) monotherapy in patients with multiple myeloma who are predominantly refractory to anti-CD38 therapy and lenalidomide. According to the company, TECVAYLI® demonstrated a 71% reduction in the risk of disease progression or death and a 40% reduction in the risk of death compared to standard of care. The safety profile was consistent with previous findings, and no new safety concerns were identified. The full results of the MajesTEC-9 study will be presented at a future major medical meeting and shared with global health authorities.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Johnson & Johnson published the original content used to generate this news brief via PR Newswire (Ref. ID: NY61551) on January 14, 2026, and is solely responsible for the information contained therein.
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