Johnson & Johnson announced new results from the Phase 2 RedirecTT-1 study, evaluating the investigational combination of TALVEY® (talquetamab-tgvs) and TECVAYLI® (teclistamab-cqyv) for treating heavily pretreated multiple myeloma patients with extramedullary disease. The study demonstrated a 78.9 percent overall response rate, indicating deep and durable responses through dual targeting of GPRC5D and BCMA. These findings suggest a potential novel, off-the-shelf treatment approach for patients with significant unmet needs. The data were presented at the 2025 European Hematology Association Congress in Milan.
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: NY10519) on June 15, 2025, and is solely responsible for the information contained therein.
Comments