SERVICES

Clinical Trials

Let’s partner to deliver patient-centric, innovative solutions that redefine the possibility of drug development. Learn how to accelerate patient recruitment and optimize protocol design while reducing patient burden and increasing retention.

Trending Topics

A Transformational Approach to Clinical Trials

LabCorp Transforms the Clinical Trial Experience to Streamline its Drug Development Process

Company goes beyond decentralized clinical trials to deliver seamless tech-enabled, patient-centric enterprise solutions. LabCorp now offers a comprehensive and fully integrated patient, site, and customer experience for DCTs.

Blog

Patient Intelligence: Designing Clinical Trials in the COVID-19 Era

In the age of COVID-19, patients can't wait for new vaccines and therapies to come to the market. That is why even in these challenging times, Covance has been focused more than ever on understanding the patient perspective on clinical trial participation. As social distancing has become the new normal, the need to understand changes in preferences associated with interest in trial participation should be taken into account when developing protocols.

Webinar

NASH Clinical Development During the COVID-19 (Coronavirus) Pandemic

The COVID-19 pandemic has brought unprecedented challenges in clinical development. Travel restrictions, social distancing and the fear of contracting the disease are impeding conventional trial conduct. Typically, routine patient and monitoring visits to healthcare facilities are now the exception, study coordinators and site staff have increased demands on their time and, in some cases, layoffs have rendered some sites incapable of continuing as usual. To help keep patients safe and allow trials to progress, regulatory authorities worldwide have issued guidance for industry, investigators and institutional review boards.

News

LabCorp Accelerates Adoption of Decentralized Clinical Trials, Expands Technology Ecosystem Through Alliance with Medable

LabCorp, a leading global life sciences company that is deeply integrated in guiding patient care, today announced that Covance, its drug development business, is expanding its technology ecosystem to accelerate the adoption of decentralized clinical trials, often referred to as hybrid and virtual clinical trials. Covance is expanding its decentralized trials technology ecosystem through an alliance with Medable, a leading software provider for digital clinical trials.

By the Numbers

3,800 Studies
64,000 Investigator Studies
660,000 Patients

Covance Clinical Development Services activity during the last 5 years.

Featured Article

Decentralized Clinical Trials – Best Practices for Designing a Flexible, Resilient Protocol

As drug development sponsors are incorporating patient-centric elements into their traditional clinical trial designs, there are several factors to consider during the study planning phase. Whether using telemedicine, mobile nursing services, laboratory support, patient service centers, investigational product management or a combination of these elements, it is important to develop an operational strategy that allows for flexibility and accounts for complete oversight of each connection point between patients, service providers and the sponsor.

Have Questions?

  • What is an FSP?

    FSP stands for functional service provider and is about delivering customized global solutions that enable clients to efficiently manage their clinical trial portfolio. This includes putting quality people, intelligent processes, and deep technical expertise in place to work directly on a client’s business. An increasing number of pharmaceutical and biotech companies are turning toward this model to decrease their overhead and make their operations leaner and more efficient. Covance FSPx® is the functional service provider you can rely on to deliver customizable solutions through strong collaboration and commitment to quality. Learn more about FSP.

  • What are Decentralized Clinical Trials, Virtual Clinical and Hybrid Clinical Trials?

    The need to transition from a site-centric approach to a more patient-centric clinical trial model led to innovations that reduce patient burden by reducing the amount of travel needed, allowing more services to be performed at or near the patients’ homes and incorporate new ways of identifying and enrolling trial participants. First called “virtual trials,” meaning investigator sites would play little role, the industry rapidly learned that most trials would involve a hybrid approach, including both traditional and novel technologies. Now this spectrum of trials is usually termed “Decentralized Clinical Trials” or DCT for short. We deliver a patient-centric ecosystem of conveniently located resources all connected by a single technology platform. An example of a DCT model is our solution that includes connecting LabCorp’s U.S.-based Patient Service Centers, global partnerships with reputable retail pharmacies, as well as home health phlebotomy and nursing service providers, with a best-in-class technology platform. We can pair site-based patient recruitment with web-based direct-to-patient outreach. Learn more about DCTs.

  • When should Phase IV trials be considered for drug development?

    Phase IV trials are conducted “in the real world.” As such, they can complement, and in certain circumstances, replace Phase III trials. If your drug is for a rare/orphan indication, a life-critical condition or where a Phase III trial would be considered unethical, a Phase IV trial may be preferable for regulators. For advanced cell and gene therapies, Phase IV trials and accompanying long-term follow-up studies should be considered. Learn more about Phase IV trials.

  • How can Phase IV studies/trials, and Phase IIIb trials be combined to explore new indications?

    Exploring new indications for previously approved products requires an appropriate level of safety and efficacy data to be collected to satisfy regulators. Depending upon the target indication, a Phase IV study may suffice to generate the real-world evidence (RWE) needed. However, where more thorough investigation is required, a Phase IIIb clinical trial or a Phase IV trial may be required. Our aim is to maximize efficiency by working with you to determine the most appropriate approach for your product and target indication.

  • How does Covance utilize proprietary data to improve clinical study outcomes?
    • Only Covance combines one of the world’s largest sources of de-identified lab results and patient intelligence data with investigator data from the majority of global clinical trials that provide insights to increase efficiencies and effectiveness in clinical drug development.
    • LabCorp Data – using LabCorp’s real-world, de-identified clinical laboratory data on over 150 million patients, we can assess populations who meet your protocol’s eligibility criteria and accurately model the impact that the protocol inclusion/exclusion criteria will have on the patient pool size.
    • Covance Central Labs Data – Covance generates more clinical trial data than anyone else in the world. Our global proprietary data helps us predict future investigator performance and capacity to run multiple studies.
    • Patient Direct – we have access to ~150 million patients and have a rapidly growing database of people who have given us permission to reach out directly to them for participation in clinical studies. Learn more.
  • What is the Covance Integrated Clinical Pharmacology Solution?

    Drug development is a complex and challenging pathway to navigate. In today’s environment with ever more complex drugs and drug targets, it is essential to think beyond the four walls of a traditional clinical pharmacology unit in order to optimize early clinical development. An integrated development platform, including the resources, experience, expertise and infrastructure necessary to design and execute early clinical studies is an effective way of mitigating risk. A multidisciplinary team that understands the market and the molecule can devise a regulatory strategy and an early clinical development plan that aims to efficiently determine whether or not a drug candidate should continue to be developed. Effective use of the integrated platform allows for efficient determination of whether or not the drug achieves sufficient levels in the relevant physiologic compartment, whether it interacts with its intended target as anticipated and whether it has any unanticipated or otherwise untoward biological effects. Increasingly, this requires not only strong clinical pharmacology expertise, but also access to biomarker testing and project management staff that can guide a protocol seamlessly from cohorts of normal healthy volunteers in a clinical pharmacology unit to cohorts of patients at multiple investigative sites. Learn more about clinical pharmacology.

Covance Insights

How the RACE for Children Act Impacts Pediatric Oncology Drug Development
How the RACE for Children Act Impacts Pediatric Oncology Drug Development
Videos & Webinars Play Video
View this webinar to get insights spanning rare diseases, regulatory strategy, oncology and pediatric drug development. Find out about the current pediatric oncology drug development landscape and an industry-focused view of applicable regulations and the RACE for Children Act.
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Mobile Health and Hybrid/Virtual Trials in Diabetes
Mobile Health and Hybrid/Virtual Trials in Diabetes
Videos & Webinars Play Video
The management landscape for Diabetes Mellitus (both Type 1 and Type 2) has changed drastically. Innovations in the mobile health technology space have allowed patients with diabetes to have improved glycemic control with more data available to them and their providers. Clinical trials in diabetes have also improved data capture, safety and accessibility using new mobile health platforms, specifically hybrid and virtual trial technology. This educational webinar will provide an overview of the mobile health technology space, highlighting current innovations and challenges. The discussion will be moderated by Dr. Barry Goldstein following presentations by Dr. Manasi Jaiman and Dr. Bola Oyegunwa.
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Inflammatory Bowel Disease clinical studies and the importance of patient centricity
Inflammatory Bowel Disease clinical studies and the importance of patient centricity
Blogs
In today's exceptionally crowded clinical trial environment of inflammatory bowel disease (IBD), patient-centric practices can help your study of Crohn's disease (CD) or ulcerative colitis (UC) stand out to both patients and sites. Learn about your options to increase your trial's patient centricity, encourage recruitment and promote ongoing patient retention.
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Addressing the Challenges of Data Management for Pharmaceutical and Biotechnology Companies: Introducing Laboratory FSPx
Addressing the Challenges of Data Management for Pharmaceutical and Biotechnology Companies: Introducing Laboratory FSPx
Blogs
The process of ensuring clinical trial records are accurate and fully reconciled between laboratory and clinical data sources can be a point of frustration for today's pharmaceutical and biotechnology companies. Whether the data is coming from a contract research organization (CRO), a central laboratory or third-party laboratories, the need for timely availability of clean data based on unique sponsor format/industry requirements has become extremely complex.
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