Clinipace Worldwide has announced that 2013 was its strongest year to date.
Clinipace Worldwide, the CRO headquartered in Research Triangle Park, North Carolina, has announced that 2013 was its strongest year to date. New clinical development projects and regulatory and strategic development engagements accounted for 114% growth in bookings compared to 2012, according to the company.
Clinipace reported 63% growth in consolidated revenues, plus 194% year-on-year growth in new bookings for full-service studies and a tripling of average contract value. It experienced solid growth in several therapeutic areas, including oncology/hematology, infectious disease, gastroenterology, cardiovascular, nephrology, immunology, pediatrics, and women’s health. One of the company’s areas of specialty is managing oncology clinical trials.
The firm hired 50 net new team members in 2013, and expects to expand by an additional 25% in 2014, especially in clinical monitoring, site management services, clinical project management, clinical data management, and financial operations.
Outside of the U.S., the CRO’s offices are located in Zurich (Switzerland), Munich (Germany), High Wycombe (U.K.), Tel-Aviv (Israel), Sao Paulo (Brazil), Buenos Aires (Argentina), and Trivandrum Kerala and New Delhi (India).
Read the full release here.
Stay current in clinical research with Applied Clinical Trials, providing expert insights, regulatory updates, and practical strategies for successful clinical trial design and execution.
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
Managing Side Effects and Dosing in Off-Label GLP-1 Use with Help from Real-World Evidence
July 18th 2025Shipra Patel, global therapeutic area section head, endocrinology, global head, pediatrics, Parexel, explains how real-world data is helping researchers navigate gastrointestinal side effects, dose flexibility, and long-term tolerability in off-label GLP-1 use.
Anselamimab Misses Primary Endpoint in Phase III CARES Trials for AL Amyloidosis
July 17th 2025In the Phase III CARES trials, anselamimab did not meet the primary endpoint for advanced-stage AL amyloidosis, but a prespecified subgroup analysis revealed meaningful improvements in survival and cardiovascular outcomes.