Medical imaging technology company Polarean Imaging plc (AIM: POLX) announced on Monday that it has expanded its Xenon MRI imaging platform into pharma-sponsored research through a new service model developed in partnership with clinical imaging intelligence company VIDA Diagnostics.
A global pharmaceutical company has selected Polarean's Xenon MRI clinical trial support services for a multicentre study evaluating an investigational lung therapy.
This double-blind, placebo-controlled study, expected to begin in Q4 2025, will assess drug-induced changes in lung function using Xenon MRI at select sites in the US and Canada. The imaging sub-study will provide insights into ventilation, membrane conductance and red blood cell transfer, enhancing pulmonary drug development.
Polarean and VIDA will deliver site qualification, training, image harmonisation and biomarker analysis, ensuring high-quality imaging data. This revenue-generating model builds on past industry collaborations, reinforcing Xenon MRI's value as a non-invasive, radiation-free tool for assessing pulmonary function with greater sensitivity than traditional tests.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA