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Labcorp Launches Global Trial Connect to Accelerate Clinical Trials

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Rhea-AI Summary

Labcorp (NYSE: LH) has launched Labcorp Global Trial Connect, a suite of digital solutions to enhance the efficiency of clinical trials. Announced on June 17, 2024, these tools aim to accelerate trial processes at investigator sites by simplifying workflows, improving patient experiences, and aiding biopharma sponsors. Key features include site enablement resources to identify study opportunities and enhance diversity, supply readiness support to prevent delays, and workflow facilitation for better data integration and error reduction. Available to current Labcorp Central Laboratory clients, these solutions promise to speed up study initiation and maintain momentum.

Positive
  • Launch of Labcorp Global Trial Connect could enhance trial efficiency, potentially speeding up market entry for therapies.
  • Site enablement resources may improve patient recruitment and diversity in clinical trials.
  • Supply readiness support aims to reduce trial delays and kit waste, improving startup efficiency.
  • Workflow facilitation features might reduce errors and queries, improving data accuracy.
  • 24/7 site support and on-demand tools could maintain study momentum, benefiting trial timelines.
Negative
  • The new solutions are only available to current Labcorp Central Laboratory clients, limiting accessibility.
  • High expectations for the new suite may not be met, potentially leading to investor disappointment.
  • Implementation and integration of new systems could present short-term operational challenges.

Insights

Labcorp's launch of Global Trial Connect could be a significant positive for the company’s financial performance. By improving clinical trial efficiency and accelerating the pace at which drugs get to market, Labcorp stands to attract more biopharma clients. This would likely increase revenue streams from central laboratory services, a core business area for the company. Furthermore, enhancements in site workflow and patient recruitment could lead to higher client retention rates, reducing churn and providing long-term revenue stability.

In the short term, the costs associated with developing and deploying these new digital and data solutions might slightly impact profit margins. However, if the platform delivers on its promises, the long-term financial benefits could more than offset these initial expenses. Investors should look at how quickly Labcorp can onboard new clients and expand usage among existing clients to gauge the platform's financial impact.

From a medical research perspective, Labcorp Global Trial Connect aims to address several pain points in clinical trials, such as delays in data collection and inefficiencies in site workflows. By enhancing patient access and increasing diversity in trials, the platform could also contribute to more robust and generalizable study results. This is particularly important as the industry faces growing scrutiny over the inclusivity of clinical research.

The ability to reduce errors and data revisions through eRequisition functionality is another significant advantage. Errors and data issues can substantially delay trial timelines, impacting both the cost and speed of bringing new therapies to market. By streamlining these processes, Labcorp not only improves efficiency but also bolsters the reliability and accuracy of clinical data, which is important for regulatory approval and subsequent commercialization.

The launch of Labcorp Global Trial Connect showcases the integration of digital and data solutions to enhance clinical trial operations. The inclusion of capabilities such as site enablement resources, supply readiness support and workflow facilitation indicates a comprehensive approach to solving complex trial management issues. These aspects can significantly reduce the traditional bottlenecks in clinical trials, like patient recruitment and data management.

However, the success of such a platform depends heavily on its user-friendliness and adaptability to various trial protocols. If the technical implementation is seamless and the learning curve for site investigators is minimal, the platform could become a staple in clinical trial management. Investors should monitor feedback from early adopters and any updates or iterations Labcorp might introduce based on user experience.

Suite of digital and data solutions designed to improve clinical trial efficiency, reduce data delays and simplify investigator site workflows

BURLINGTON, N.C. , June 17, 2024 /PRNewswire/ -- Labcorp (NYSE: LH), a global leader of innovative and comprehensive laboratory services, announced today the launch of Labcorp Global Trial Connect, a suite of central laboratory solutions aimed at increasing the speed of clinical trials where the heart of clinical research is conducted – investigator sites.

"The patient-investigator-biopharma sponsor relationship is at the foundation of a successful clinical trial. Global Trial Connect simplifies the investigator workflow, improves the patient experience and ultimately enables biopharma sponsors to bring therapies to market faster," said Jon DiVincenzo, EVP and President, Central Laboratories and International at Labcorp.  "As the world's leading central laboratory, Labcorp is dedicated to improving the pace of clinical trials focusing on the investigator site experience from study initiation to patient recruitment and data collection."

Labcorp Global Trial Connect, available to current Labcorp Central Laboratory clients, incorporates complementary digital and data solutions that help accelerate clinical study startup, maintain study momentum and increase study throughput. Capabilities include:

  • Site enablement resources – to identify new study opportunities, enhance patient access and recruitment and improve diversity in clinical trials.
  • Supply readiness support – to increase study startup efficiencies, reduce trial delays and reduce supply and kit waste.
  • Site workflow facilitation – to help integrate sample collection and tracking data, provide visibility and actionable analytics to both sites and sponsors, and reduce errors, queries, holds and data revisions through eRequisition functionality.
  • Study management and investigator support – to accelerate study startup and maintain study momentum with 24/7 site support and on-demand tools and trainings.

For more information, visit LabcorpGlobalTrialConnect.com.

About Labcorp
Labcorp (NYSE: LH) is a global leader of innovative and comprehensive laboratory services that helps doctors, hospitals, pharmaceutical companies, researchers and patients make clear and confident decisions. We provide insights and advance science to improve health and improve lives through our unparalleled diagnostics and drug development laboratory capabilities. The company's more than 67,000 employees serve clients in approximately 100 countries, provided support for 84% of the new drugs and therapeutic products approved in 2023 by the FDA, and performed more than 600 million tests for patients around the world. Learn more about us at www.labcorp.com.

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/labcorp-launches-global-trial-connect-to-accelerate-clinical-trials-302174129.html

SOURCE Labcorp

FAQ

What is Labcorp Global Trial Connect?

Labcorp Global Trial Connect is a suite of digital and data solutions designed to accelerate clinical trials by improving efficiency, reducing data delays, and simplifying workflows at investigator sites.

When was Labcorp Global Trial Connect launched?

Labcorp Global Trial Connect was launched on June 17, 2024.

What are the key features of Labcorp Global Trial Connect?

Key features include site enablement resources, supply readiness support, workflow facilitation, and 24/7 site support with on-demand tools and training.

Who can access Labcorp Global Trial Connect?

Labcorp Global Trial Connect is currently available to existing Labcorp Central Laboratory clients.

How might Labcorp Global Trial Connect benefit clinical trials?

The suite aims to improve patient recruitment, enhance data accuracy, reduce trial delays, and maintain study momentum, potentially speeding up the market entry of therapies.

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