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Velocity Clinical Research Appoints Former Fortrea Executive, Andrew Reina, as Chief Revenue Officer
Globenewswire· 2025-11-12 12:06
Core Insights - Velocity Clinical Research has appointed Andrew (Drew) Reina as Chief Revenue Officer, effective immediately, to enhance its strategic partnerships and revenue growth [1][2][3] Company Overview - Velocity is a leading integrated site organization for clinical trials, operating over 70 sites with more than 200 investigators, partnering with pharmaceutical and biotechnology companies [7] - The company aims to set the standard for strategic relationships between multisite clinical research corporations, Sponsors, and CRO partners [2] Leadership and Experience - Drew Reina brings over two decades of global clinical research experience, previously serving as Vice President and Head of Sales at Fortrea, where he led a high-performing commercial organization [4][5] - His experience includes overseeing a $1 billion+ global portfolio at PPD's Biopharma segment, focusing on strategic partnerships and alliance management [5] Strategic Goals - As CRO, Drew will drive growth through strategic partnerships with Sponsors and CROs, aligning business development, marketing, and network operations to ensure consistent revenue performance [6] - The organization is positioned to meet the evolving needs of clinical research, helping to accelerate speed to market and alleviate burdens on sites and patients [4][6] Technological Advancements - Velocity operates a technology hub in India, developing innovative systems to leverage expansive site, patient, and historical performance data, enhancing efficiency in clinical trials [8]
医疗保健动态:人工智能能否让临床试验变得更好-Weekend Healthcare Pulse_ Can artificial intelligence make clinical trials better_
2025-08-18 02:52
Summary of Clinical Trials and AI Integration Industry Overview - The focus is on the clinical trials industry, which is facing challenges related to cost and efficiency, with a growing interest in integrating artificial intelligence (AI) to improve processes [1][8][9]. Key Points and Arguments Challenges in Clinical Trials - Clinical trials are costly and inefficient, with costs exceeding $2.5 billion for drug development [4]. - A study found that 54% of phase 3 trials fail, primarily due to insufficient efficacy (57%) and safety concerns (17%) [3]. - Recruitment issues are significant, with only 31% of UK trials meeting enrollment targets [4]. - From 2012 to 2022, R&D spending increased by 44%, yet the number of novel drug approvals remained flat, leading to higher average drug development costs [5]. - As of 2024, it is estimated that up to 80% of clinical trials exceed their forecasted timelines [5]. Potential of AI in Clinical Trials - AI is believed to have the potential to enhance various stages of clinical trials, including trial design, site selection, recruitment, monitoring, and analysis [9][10]. - AI can analyze real-world data (RWD) to improve trial design by refining patient eligibility criteria and optimizing endpoints [12]. - In site selection, AI can predict enrollment numbers and identify optimal trial locations, thus reducing costs and improving speed [14]. - For recruitment, AI can create comprehensive patient profiles from diverse data sources, improving eligibility matching and targeting underrepresented populations [16]. - AI can enhance monitoring by tracking site performance metrics in real-time, allowing for early identification of operational risks [18]. - In the analysis phase, AI can accelerate data cleaning and identify treatment effects that traditional methods may miss [20]. Companies Utilizing AI in Clinical Trials - A variety of companies are integrating AI into clinical trials, categorized into three groups: 1. **Full-fledged CROs**: Companies like IQVIA, Icon, and Fortrea are developing AI tools to enhance their internal trial processes [24]. 2. **Health-tech Companies**: Firms such as Medidata, ConcertAI, and Flatiron Health offer software platforms that utilize AI for various trial stages [24]. 3. **Diagnostics Companies**: Tempus and Caris Life Science focus on in-house sequencing and real-time patient matching [24]. Data and Partnerships - High-quality data is crucial for building effective AI models, with companies emphasizing the size and quality of their datasets [30][31]. - Partnerships are essential for enhancing datasets and improving AI models, with companies collaborating to combine resources and expertise [37][39]. Other Important Insights - The clinical trial industry is in the early stages of AI integration, with significant potential for transformation but also challenges due to regulatory complexities [39][40]. - The need for innovation in clinical trials is critical, whether through AI or other means, to address rising costs and operational inefficiencies [40]. This summary encapsulates the current state of the clinical trials industry, the challenges it faces, the potential role of AI, and the companies leading the charge in this transformation.
Avant Technologies and Ainnova Tech Announce Enhanced Patient Recruitment Strategy Ahead of FDA Clinical Trial
Prnewswire· 2025-08-12 12:00
Core Insights - Avant Technologies Inc. and Ainnova Tech, Inc. are collaborating on a clinical trial for the Vision AI platform aimed at early detection of diabetic retinopathy [1][4] - Ainnova is refining its patient recruitment strategy to include approximately 1,000 multiethnic patients, focusing on community clinics rather than specialized centers [2][3] - The partnership with Fortrea, a recognized Contract Research Organization, is expected to enhance the quality and efficiency of the clinical study [4][5] Company Overview - Avant Technologies Inc. is an emerging technology company focused on healthcare solutions utilizing artificial intelligence and biotechnology [7] - Ainnova Tech, Inc. is a healthtech startup dedicated to leveraging AI for early disease detection, with a specific focus on preventing blindness related to diabetes [6] Clinical Trial Details - The clinical study will take place at 8-10 sites across the U.S., targeting a diverse patient population to ensure the data reflects real-world scenarios [2][3] - The study's design aims to support the FDA 510(k) submission, which is crucial for regulatory approval and market entry [4][5] Strategic Importance - The success of the clinical trial is vital for Ainnova's technology portfolio, particularly for entering the U.S. market, which presents significant commercial potential [5]