WAYNE, Pa. and BOSTON, June 22, 2015 /PRNewswire/ -- Bracket Global, LLC and Clintara are pleased to announce the two companies have agreed to combine. Bracket will integrate the Clintara platform of surveillance strategies developed for clinical trials within Bracket's proprietary electronic platform for Clinical Outcome Assessments (eCOA). The integration will include Clintara's innovative C-VISA Subject Eligibility Validation program designed to ensure appropriate patients are enrolled in clinical trials.
Bracket CEO Jeff Kinell stated, "I am impressed by the culture, business practices, and scientific innovation reflected in Clintara's steady growth and impact on our industry. I am truly excited about our future opportunities together."
Founded in 2009 by Steven D. Targum, MD, Clintara's methodology and technology includes audio-digital pen recordings of site-based interviews and site-independent "dual" scoring reviews. The Clintara surveillance strategy has enhanced ratings precision and improved the data integrity of clinical trials.
The Clintara leadership will assume expanded roles within Bracket. Dr. Targum will become the Scientific Director of Bracket and will work closely with Bracket's Senior Vice President and Chief Medical Officer, David Daniel, MD. Clintara CEO Colin Bower will become Vice President, Scientific Services and will work with the Bracket leadership team and Scientific Advisory Board to develop cutting-edge solutions to improve the conduct of clinical trials.
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.
Reaching Diverse Patient Populations With Personalized Treatment Methods
January 20th 2025Daejin Abidoye, head of solid tumors, oncology development, AbbVie, discusses a number of topics around diversity in clinical research including industry’s greatest challenges in reaching diverse patient populations, personalized treatment methods, recruitment strategies, and more.
Phase III Trial Data Show Subcutaneous Pembrolizumab as Noninferior to IV Keytruda
March 31st 2025Subcutaneous administration of pembrolizumab with chemotherapy demonstrated a nearly 50% reduction in patient chair and treatment room time while maintaining efficacy and safety endpoints compared to intravenous Keytruda.
Phase II ALPACA Trial Shows Lepodisiran Produces Significant, Sustained Lipoprotein(a) Reductions
March 31st 2025Eli Lilly’s lepodisiran, an investigational siRNA therapy, achieved significant and durable reductions in lipoprotein(a) levels, a major genetic risk factor for cardiovascular disease.