
US healthcare giant Johnson & Johnson (NYSE: JNJ) has announced new data from the investigational Phase III MajesTEC-3 study showing the potential of Tecvayli (teclistamab) plus Darzalex subcutaneous (daratumumab SC) formulation as early as second line for patients with relapsed/refractory multiple myeloma (RRMM).
Results show an 83.4% reduction in the risk of disease progression or death compared to standard regimens at nearly three years follow-up. More than 90% of patients who were progression-free at six months remained progression-free at three years.
The study evaluated the efficacy and safety of the investigational immunotherapy combination of teclistamab plus daratumumab SC versus daratumumab SC and dexamethasone with either pomalidomide or bortezomib in patients with RRMM who have received one to three prior lines of therapy.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
| Headless Content Management with Blaze