ACR Image Metrix
™ is pleased to announce that the DCE-MRI study, as commissioned by
Bionomics Ltd.
, was submitted as an abstract by Bionomics to the American Society of Clinical Oncology (ASCO) and has been accepted to be presented as a part of the scientific program during the general poster session at the
ASCO Annual Meeting
, which will take place June 4-8, 2010, in Chicago, Illinois, at McCormick Place.
As a drug discovery and development organization focusing on new treatments for cancer and serious disorders of the central nervous system, Bionomics selected ACR Image Metrix to perform the imaging components of this study.
“Their extensive experience in the utilization of novel imaging techniques to serve as biomarkers and history of partnering with regulatory agencies to develop standards for imaging acquisition, data normalization, data extraction and the assessment of variability made the selection of ACR Image Metrix as our imaging CRO appropriate for this project,” stated Bionomics Vice President of Discovery Research, Gabriel Kremmidiotis, Ph.D.
The completion of this Phase I clinical trial, which involved
MRI (DCE-MRI)
quantitative analysis, was a two-stage dose escalation design involving Bionomics’ BNC 105P-001, a novel vascular disrupting agent staged in patients with advanced solid tumors.
“Teaming up with Bionomics to complete this study turned out to be a success and we are pleased with the results. This is a major milestone for ACR Image Metrix in our ability to conduct novel imaging for both pharmaceutical and biotech companies,” stated General Manager of ACR Image Metrix, Michael J. Morales.
ACR Image Metrix will also be exhibiting at the ASCO Annual Meeting, Booth 19097.
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
Gilead Shares Final Data from Phase III MYR301 Trial of Bulevirtide in Chronic Hepatitis Delta Virus
May 7th 2025Long-term results from the study show 90% of patients with chronic HDV who achieved undetectable HDV RNA at 96 weeks of treatment remained undetectable for nearly 2 years post-treatment.