Precision radiation medicine company Elekta AB (STO:EKTAB.ST) announced on Monday the signing of a contract with the Institut Jules Bordet, Brussels, for an Elekta Unity MR-linac system, two Versa HD linear accelerators (linacs) and an upgrade of existing Elekta Infinity linacs, as well as upgrades and expansions of Monaco treatment planning software and MOSAIQ oncology information systems and service.
This contract has a total valued of approximately EUR22m, of which EUR18m will be booked in the third quarter of Elekta's fiscal year 2019/20. The remainder will be booked successively over the next 10 years. Elekta won the contract through a public procurement procedure.
Reportedly, this comprehensive cancer centre is gearing up for its new cancer clinic with an investment in state-of-the-art technology and upgrades to existing devices. This includes Elekta Unity, a transformative magnetic resonance radiation therapy (MR/RT) system, which combines a high-field MRI scanner with a best-in-class linear accelerator to enable personalised precision radiation therapy.
The institute already employs Elekta solutions, including Leksell Gamma Knife Icon and two Elekta Infinity linacs, as well as MOSAIQ and Monaco and Elekta's microSelectron brachytherapy afterloading platform. The two Versa HD systems in this contract will replace competing systems.
Upon full deployment of all the solutions, the Jules Bordet Institute is expected to become Belgium's largest single radiation therapy site with four Elekta linacs, one Unity MR-Linac and one Leksell Gamma Knife.
According to Elekta, software upgrades are scheduled for delivery during 2020 and the linear accelerators, including Unity, in 2021.
Elekta, a provider of precision radiation medicine, offers cancer patients more precise, personalized radiotherapy treatments.
Biovica secures European patent for biomarker use in immuno-oncology
Valneva signs exclusive German vaccine distribution deal with CSL Seqirus
Accord Healthcare introduces Dehydrated Alcohol Injection for cardiovascular indications
CARsgen Therapeutics' satri-cel NDA accepted by Chinese regulator
Alvotech reports positive topline results for Xolair biosimilar study
Sanofi receives FDA orphan drug designation for riliprubart in transplant rejection
Scancell expands Phase 2 SCOPE trial with new intradermal dosing arm for iSCIB1+
Telix Pharmaceuticals delivers first commercial doses from Belgian manufacturing hub
Innovent presents mazdutide Phase 3 clinical study results at ADA 85th Scientific Sessions
Hoth Therapeutics reports positive interim results for HT-001 topical therapy
Breckenridge Pharmaceutical's generic for Ablysinol granted final FDA approval
Aiforia Technologies launches CE-IVD marked AI solution for breast cancer diagnostics
Stockholders approve proposed merger of TuHURA Biosciences and Kineta