Human care company Elekta AB (STO:EKTAB.ST) announced on Monday that its Elekta Unity magnetic resonance radiation therapy (MR/RT) system has received the CE mark, clearing the technology for commercial sales and clinical use in Europe.
According to the company, Unity has the potential to transform how clinicians treat cancer by enabling the delivery of the radiation dose while simultaneously visualising the tumour and surrounding healthy tissue with high-quality MR images.
Also, Unity integrates advanced tools that allow clinicians to adapt the patient's treatment to this current anatomical information.
Elekta added that although the Unity has CE mark, it is not available for commercial distribution or sale in the US.
Elekta's treatment solutions and oncology informatics portfolios are designed to enhance the delivery of radiation therapy, radiosurgery and brachytherapy, and to drive cost efficiency in clinical workflows.
AbbVie and Iambic agree collaboration for discovery and development of small molecule therapies
Grunenthal to acquire Stivarga cancer treatment
Precigen announces FDA platform technology designation for AdenoVerse
Enhertu recommended for EU approval in early HER2-positive breast cancer
PureTech receives FDA Fast Track designation for LYT-200 in HR-MDS
Coiled Therapeutics completes enrolment in two AO-252 formulation cohorts
Myosin Therapeutics chosen for 2026-2027 NCI Investor Initiatives Showcase
GSK to acquire trispecific T cell-engager from Chimagen for multiple myeloma
Kelun-Biotech publishes phase III data for trastuzumab botidotin in HER2-positive breast cancer
AstraZeneca's Etcamah misses primary endpoint in Phase III breast cancer trial
GSK reports positive Jideytro data supporting potential first-line lung cancer use
Akeso presents positive results from registrational Phase III study of ivonescimab
ABL Diagnostics files bid to acquire IntegraGen
Tyra Biosciences declares positive Phase 2 results for oral dabogratinib in bladder cancer