Citeline Data Shows Higher Rate of Transparency Commitment
Citeline reported that clinical trial transparency is in a much healthier state than shown in previous studies.
Citeline, a pharmaceutical industry research provider on clinical trials, reported that clinical trial transparency, also known as responsible data sharing, is in a much healthier state than shown in previous studies. Doro Shin, a Citeline analyst, presented the findings of her analysis at an event for competitive intelligence experts in the pharmaceutical industry. For her analysis, Ms. Shin used Citeline's Trialtrove, a competitive intelligence resource which draws data from over 30,000 sources. The analysis focused on nearly 7,500 Phase II-III industry sponsored trials with primary completion dates between 2008 and 2012, to determine how many of these trials provided results in peer reviewed sources (defined as a journal manuscript or conference abstract) or at clinicaltrials.gov.
Out of all the Phase II-III studies reviewed, a surprising 78% provided final or interim results across all sources. When looking just at the Phase III trials, the most expensive and high profile trials for sponsor companies, this number improves and 81% provide final or interim results. Prior industry analyses found that 23-57% of completed clinical trials do not report results.
Read the full release here.
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.
