The latest news for pharma industry insiders.
DIA 2024: Machine Learning and Simulations to Facilitate Clinical Trials
In a session at the 2024 DIA Global Annual meeting in San Diego, CA, Raviv Pryluk, CEO & co-founder, PhaseV; Sam Miller, head of strategic consulting, Exploristics; and Andrew Stelzer, head of business development, Unlearn.ai addressed a number of ways simulations are currently being utilized in clinical research.
Young Adults with Type 1 Diabetes Have Suboptimal Glucose Control
Researchers suggest younger people with diabetes need more education and better support to manage their diabetes.
Establishing a Data Ecosystem Using Automation to Optimize Regulatory-Compliant Clinical Trials
Significant advances in technology are providing new opportunities to collect and utilize real-world data to establish better clinical trial protocols that have a patient-centric focus and the ability to transform healthcare. However, it is important to understand how such applications work and their impact on safety.
This webcast series uncovers the concerns of safety professionals and other stakeholders involved in the development and implementation of clinical trial protocols in the digital era and highlights methods to best apply digital data into routine practice to best optimize trial success and adhere to strict regulatory guidance.
How A.I. Is Revolutionizing Drug Development
In high-tech labs, workers are generating data to train A.I. algorithms to design better medicine, faster. But the transformation is just getting underway.
A new study “Self-administered gerocognitive examination (SAGE) aids early detection of cognitive impairment at primary care provider visits” published today in Frontier in Medicine by researchers at The Ohio State University Wexner Medical Center finds that the practical and brief SAGE test was easily incorporated into primary care providers’ visits. This screening tool resulted in a significant increase in the detection of cognitive concerns.
Silence Therapeutics plc on LinkedIn
Discover how Craig Tooman, President and CEO, navigated the #biotechsector's post-pandemic funding challenges to strengthen Silence’s position in the #siRNAdrug field in this interview with Pharmaceutical Executive : https://bit.ly/45r9zOF
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Key Findings of the NIAGARA and HIMALAYA Trials
November 8th 2024In this episode of the Pharmaceutical Executive podcast, Shubh Goel, head of immuno-oncology, gastrointestinal tumors, US oncology business unit, AstraZeneca, discusses the findings of the NIAGARA trial in bladder cancer and the significance of the five-year overall survival data from the HIMALAYA trial, particularly the long-term efficacy of the STRIDE regimen for unresectable liver cancer.
Fake Weight Loss Drugs: Growing Threat to Consumer Health
October 25th 2024In this episode of the Pharmaceutical Executive podcast, UpScriptHealth's Peter Ax, Founder and CEO, and George Jones, Chief Operations Officer, discuss the issue of counterfeit weight loss drugs, the potential health risks associated with them, increasing access to legitimate weight loss medications and more.
Johnson & Johnson Seeks FDA Approval for Subcutaneous Tremfya Regimen for Ulcerative Colitis
November 22nd 2024Johnson & Johnson has submitted a supplemental Biologics License Application to the FDA for a subcutaneous induction regimen of Tremfya for adults with moderately to severely active ulcerative colitis based on positive Phase III ASTRO trial results.