• SKIP TO CONTENT
  • SKIP NAVIGATION
  • Patient Resources
    • COVID-19 Patient Resource Center
    • Clinical Trials
    • Search Clinical Trials
    • Patient Notification System
    • What is Clinical Research?
    • Volunteering for a Clinical Trial
    • Understanding Informed Consent
    • Useful Resources
    • FDA Approved Drugs
  • Professional Resources
    • Research Center Profiles
    • Clinical Trial Listings
    • Market Research
    • FDA Approved Drugs
    • Training Guides
    • Books
    • eLearning
    • Events
    • Newsletters
    • White Papers
    • SOPs
    • eCFR and Guidances
  • White Papers
  • Trial Listings
  • Advertise
  • COVID-19
  • iConnect
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » Sanofi teams up with Medco Health Solutions, UBC

Sanofi teams up with Medco Health Solutions, UBC

June 24, 2011
CenterWatch Staff

Sanofi is looking for more ‘real-world’ insight into its drug development and product lifecycle strategies by teaming up with pharmacy benefit manager Medco Health Solutions to help deliver value propositions that can withstand tough scrutiny from regulators and payers, reports PharmaTimes.

The global, multi-year agreement between Sanofi, Medco Health Solutions and Medco’s wholly owned subsidiary United BioSource Corp. (UBC) is designed to support real-world evidence assessments during Sanofi’s product development and pre-/post-approval processes, underpinning improvements in the overall quality of patient care. Details of the arrangement were not released.

According to the new partners, the agreement will enable Sanofi to identify more precisely patient populations with the greatest unmet medical need and will help to determine in which populations drugs will be most effective.

It will also generate real-world comparative effectiveness data to support product value that can satisfy stakeholder evidence requirements, the companies said.

The aim is to build a “consolidated representation” of payer, manufacturer and researcher insight throughout the product lifecycle, to support improved health outcomes and deliver “meaningful” benefits to patients, healthcare providers and payers. 

“Some products that seemed to hold promise in early research might not deliver the intended results when used in real-world practice,” said Dr. Robert Epstein, Medco’s clinical R&D officer. “This partnership will use real-world evidence to develop products that demonstrate value in real-world settings, enabling Sanofi to support high-quality, cost-effective care.”

Medco and UCB offer “robust capabilities to help us close the gap between R&D and the real-world clinical setting,” said Sanofi’s chief medical officer, Jean-Pierre Lehner. “Through this agreement, we will make the leap from discovering and marketing new medicines to providing comprehensive healthcare solutions that are proven to drive safety, effectiveness and relative value for our stakeholders.”

The partners cited Medco’s and UCB’s resources in real-world evidence, comparative effectiveness, personalized medicine/pharmacogenomics, health economics, safety research and clinical/adherence support.  

 

Upcoming Events

  • 16Feb

    Fundamentals of FDA Inspection Management: Reduce Anxiety, Increase Inspection Success

  • 21May

    WCG MAGI Clinical Research Conference – 2023 East

Featured Products

  • Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

    Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

  • Surviving an FDA GCP Inspection

    Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs

Featured Stories

  • SurveywBlueBackground-360x240.png

    Sites Name Tech Acceptance as Essential Factor in Selection of Sponsors, Survey Finds

  • TrendsInsights2023-360x240.png

    WCG Clinical Research Trends and Insights for 2023, Part Two

  • TimeMoneyEffort-360x240.png

    Time is Money and So Is Effort, Budgeting Experts Say

  • TrendsInsights2023A-360x240.png

    WCG Clinical Research Trends and Insights for 2023, Part Three

Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials

The information you need to adapt your monitoring plan to changing times.

Learn More Here
  • About Us
  • Contact Us
  • Privacy Policy
  • Do Not Sell or Share My Data

Footer Logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 617.948.5100 – Toll free 866.219.3440

Copyright © 2023. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing