Merger offers customers international reach combined with specialized oncology expertise for clinical trial development and implementation
CYPRESS, CA. - WCCT Global, an international specialized clinical research organization (CRO), and Medelis, Inc., a specialty oncology CRO, announced today that the companies have merged to offer US and international clients access to an expanded depth and breadth of clinical research offerings. "The complex and rapidly growing oncology drug development market in the US, Europe, and Asia requires unique insight and expertise and an eye toward the future, all of which we now offer through this merger," said Dr. Kenneth Kim, founder and CEO of WCCT Global. "We're committed to delivering world-class clinical research solutions to achieve our vision of becoming the global leader in the development of specialized medicines and therapies." Medelis will continue to provide the highest quality clinical research for all of Medelis' current and future studies. Bill Taaffe, the current president of Medelis and former president and CEO of ICON Clinical Research-US, will continue to lead Medelis. "We now offer the solution for the many sponsors who have been asking for a single specialty oncology CRO to help them navigate all of the complexities of taking oncology and immuno-oncology drugs into the clinic in the US, Europe, and Asia," said Bill Taaffe, president of Medelis. WCCT Global offers in-house project management, clinical monitoring, biostatistics and data management, an extensive investigator and patient recruitment network, clinical pharmacology units, and a translational medicine team for handling all aspects of regulatory affairs. The merger adds to these corporate offerings the extensive oncology expertise of Medelis and the experience of designing and managing preclinical and phase 1 through phase 4 studies at over 400 sites in North America and Europe. "The addition of Medelis not only creates a more robust offering for our current and future clients, it also creates a stronger company with multiple synergies to fuel our future growth," stated Ron Linares, CFO of WCCT Global.
About WCCT Global
WCCT Global
is a specialized CRO delivering early drug development and late phase CRO services to the pharmaceutical, biotechnology, and medical device industries. As a drug development partner, WCCT Global works with domestic and foreign companies to deliver regulatory guidance, program management, patient recruitment, data management, and strategic consulting, with an emphasis in special disease populations, pediatric populations, ethno-bridging, and cardiac safety. WCCT is a leader in healthy volunteer studies, including first-in-human (FIH), as well as specific therapeutic expertise in allergy, asthma, HCV, ophthalmology, renal, and vaccines.
About Medelis, Inc.
Medelis
is a specialty oncology CRO focused on preclinical and phase 1 through phase 4 oncology trials in North America and Europe. Founded in 2003, Medelis provides sponsors with oncology expertise from drug development thought-leadership to a highly skilled clinical operations team, handling complex oncology trials in all indications, including cutting-edge immunotherapy treatments.
Unlock Commercial Growth through Data-Driven Patient and HCP Insights
May 2nd 2025Leveraging data-driven patient and healthcare provider (HCP) insights, including social drivers of health (SDOH), is essential for life sciences companies to continuously improve patient engagement and commercial success. Mark Rodgers, AVP of Commercial Analytics at Inovalon, discusses how identifying treatment milestones, assessing HCP performance, and segmenting patient populations using SDOH data can drive targeted strategies that improve healthcare outcomes and market access
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.
FDA Approves Nipocalimab for the Treatment of Generalized Myasthenia Gravis
April 30th 2025Approval is based on results from the pivotal Vivacity-MG3 trial in which IMAAVY (nipocalimab-aahu) demonstrated superior disease control throughout 24 weeks when compared to placebo plus standard of care.