Gen-Probe Life Sciences Ltd. has completed the consolidation of its Molecular Genetic Services (MGS) business at its newly expanded facilities in Manchester.
Gen-Probe Incorporated has expanded its footprint in Wythenshawe, Manchester from 11,000 sq ft to 67,000 sq ft. Among other benefits, the expansion of the facility will provide the catalyst for theconsolidation and further development of a suite of outsourced genomic services. Gen-Probe Life Sciences Ltd. will further develop its suite of genomic services aimed specifically at the R&D stage of drug development. These services will provide support to translational research through the discovery, qualification, and validation of biomarkers and IUO assays with the potential for both drug development and companion diagnostic applications.
David Scott, Senior Director, commercial services and Diaclone, said, “We are excited to beimplementing this next stage in the strategic development of our pharma services brand. We believe that the potential to identify and develop both genomic and proteomic assays for biomarkers at an early stage presents a real value proposition to biopharmaceutical companies seeking companion diagnostics.”
As part of this consolidation, Gen-Probe Life Sciences Ltd. has appointed Dr. Bob Holt as MGS manager responsible for the growth and development of the MGS business, and Haroon Allybacus as business development manager for its pre-clinical, clinical, and cGMP drug development services.
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
FDA-Approved Gene Therapy Beqvez Shows Sustained Efficacy, Safety in Long-Term Hemophilia B Trial
April 17th 2025Beqvez (fidanacogene elaparvovec), an FDA-approved one-time gene therapy for hemophilia B, demonstrated sustained factor IX expression, low bleeding rates, and a favorable safety profile over long-term follow-up.