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ÃÛÌÒ´«Ã½ experts frequently author or contribute to industry trade press.
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The rise of GLP-1 agonist therapies has transformed obesity treatment, delivering unprecedented results and revealing their potential across a spectrum of interconnected conditions. New data reveals how the breakthrough has sparked a major shift toward multi-indication drug development.
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Discover how clinical trial tokenisation helps sponsors gain patient insights and enable long-term data collection¡ªwithout adding burden to patients or sites.
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Drug pricing and reimbursement constraints are a major concern for the pharmaceutical industry. Companies must consider price and reimbursement across multiple countries, act early in the development cycle and ensure the evidence required to support their commercial strategy is built into their development plans.
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Clinical trial designs for obesity treatments should accommodate candidate drugs that have the potential to treat multiple conditions, or developers risk missing opportunities, according to Irish CRO ÃÛÌÒ´«Ã½.
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In this DDW article, discover key findings of an ÃÛÌÒ´«Ã½ survey focusing on multi-indication cardiometabolic R&D for therapies targeting obesity and its comorbidities.
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ÃÛÌÒ´«Ã½ maintains its place as the most active contract research organization (CRO) for Q1 2025.
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ÃÛÌÒ´«Ã½ survey shows pharma's enthusiasm for multi-indication obesity trials is outpacing trial design readiness.
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Meeting the demand for clinically relevant neurodegenerative treatments requires a paradigm shift in how central nervous system (CNS) clinical trials have been designed and executed. Bill Holt outlines how drug developers are now at the forefront of adopting more nuanced, cost-effective, and patient-centric clinical trial designs.
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In this article, Rose Kidd, President of Operational Delivery, discusses how greater support for women in leadership and research is helping to shape a stronger future for the pharma industry.
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Every clinical trial has challenges, but trials researching SaMD use to treat mental health disorders have unique ethical, regulatory and technical ones. In this Applied Clinical Trials article ÃÛÌÒ´«Ã½¡¯s Devin Ridgley and JoAnne Bronikowski explore the implications of a vulnerable patient population and new technology.