LaunchTrends®: Lemtrada (US) is a four-wave syndicated report series that specifically tracks the introduction of Lemtrada, a potent, intravenous disease-modifying therapy (DMT) approved to treat relapsing forms of multiple sclerosis (MS). This report series is based on primary research data collected at one month, three months, six months, and one year post-commercial availability of Lemtrada. Along with awareness and sources of familiarity, the reports assess U.S. neurologists’ trial, adoption, and use of Lemtrada, including anticipated future trends. The reports also provide information on product perception, satisfaction, obstacles to use, drivers of prescribing, patient types, displacement of competitors, Genzyme’s promotional efforts, and benchmarking against other previously launched MS agents.

Questions Answered:

  • Genzyme launched Lemtrada in the U.S. market as a treatment for relapsing forms of MS in December 2014. What is neurologists’ level of awareness of and familiarity with Lemtrada over the course of the following year?
  • Lemtrada enters an increasingly crowded MS therapy market; there are ten branded DMTs, four of which launched in the past five years. What are the perceived clinical advantages and disadvantages of Lemtrada compared with other marketed MS agents? How are the trial and adoption of Lemtrada tracking compared with other recent product launches for MS?
  • Because of its safety profile, Lemtrada’s U.S. label recommends that it should generally be reserved for later-line treatment of relapsing forms of MS. Where do neurologists expect Lemtrada to fit in the MS treatment algorithm? What are the current prescribing trends among DMTs, and how do neurologists anticipate they will change over the next six months?
  • Lemtrada is Sanofi/Genzyme’s second entrant into the MS market, following the companies’ 2012 launch of Aubagio. What promotional messages and activities is Genzyme using to support Lemtrada’s launch?

Scope: 

Markets covered: United States.

Primary research: 74 neurologists surveyed per report Wave; 10 qualitative interviews with a subset of survey respondents.

Indication coverage: Relapsing-remitting MS.

Table of contents

  • Multiple Sclerosis - Emerging Therapies - Lemtrada Launch Tracking Wave 3 (US)
    • Key Findings
      • Awareness and Perceptions of Lemtrada
      • Current Lemtrada Trial and Use
      • Lemtrada Positioning in the Competitive Landscape
      • Anticipated Lemtrada Trial and Use
    • Benchmarking Lemtrada Launch Success vs. MS Analogs
      • Prescriber and Nonprescriber Profiles
        • Lemtrada: Differences Between Prescriber and Nonprescriber Profiles
      • Lemtrada Awareness and Perceptions
        • Unaided and Aided Awareness of Lemtrada
          • Aided Awareness of Lemtrada
        • Familiarity with Lemtrada
          • Awareness of Lemtrada Indication*
          • Awareness of Lemtrada Administration*
          • Awareness of Lemtrada Dosing Interval*
        • Sources of Familiarity with Lemtrada
          • Initial Reaction to and Interest in Lemtrada
            • Initial Reaction to and Interest in Learning More About Lemtrada
            • Lemtrada Product Profile
            • Lemtrada Product Profile
            • Initial Reaction to Lemtrada
            • Interest Level in Lemtrada
          • Impressions of Lemtrada
            • Clinical Interchangeability of Lemtrada and DMT Brands
            • Statement Agreement Regarding Lemtrada
            • Statement Agreement Regarding Lemtrada
            • Lemtrada Statement Agreement: Wave over Wave
            • Uniqueness of Lemtrada vs. Currently Available Treatments
            • Lemtrada Risk-Benefit Profile Balance
            • Qualitative Interview Follow-Ups
            • Qualitative Interview Follow-Ups
          • Prescriber and Nonprescriber Profiles
            • Lemtrada: Differences Between Prescriber and Nonprescriber Profiles
        • Lemtrada Trial and Use
          • Willingness to Prescribe Lemtrada
            • Lemtrada Trial
            • Impact of Lemtrada Attributes on Willingness to Prescribe: Wave over Wave
            • Potential Issues Affecting Willingness to Prescribe Lemtrada: Wave over Wave
            • Qualitative Interview Follow-Ups
          • Number of Patients Currently Receiving Lemtrada
            • Percentage of Physicians Receiving Patient Inquiries for Lemtrada in the Past Month
            • Action Based on Specific Lemtrada Patient Requests
            • Qualitative Interview Follow-Ups
            • Mean Lemtrada Patient Volume Among Lemtrada Prescribers
            • Circumstances of Initial Lemtrada Prescriptions*
            • Current Lemtrada Status
            • Lemtrada Prescribing by Disease Classification Among Current Prescribers
            • Lemtrada Patient Origination
            • Qualitative Interview Follow-Ups
            • Course of Lemtrada Treatment Among Current Prescribers
            • Severity of Infusion-Associated Reactions to Lemtrada
            • Percentage of Patients on Lemtrada Seen for Follow Up
            • Response to Lemtrada Treatment
          • Reasons for Not Yet Prescribing Lemtrada
            • Anticipated Lemtrada Prescribing Time Frame Among Nonprescribers
          • Anticipated Lemtrada Use
            • Anticipated RR-MS DMT Treatment Rate: Next Six Months
            • Lemtrada Prescriber Base: Current, Next Six Months, and Ever
            • Potential Peak Share* for Lemtrada
            • Characteristics of Lemtrada Candidates
            • Characteristics of Lemtrada Candidates
            • Qualitative Interview Follow-Ups
          • Lemtrada Performance on Key Attributes
            • Lemtrada Performance Ratings and DMT Choice Attribute Importance Ratings
            • Lemtrada Performance Ratings and DMT Choice Attribute Importance Ratings
            • Overall Lemtrada Satisfaction
        • Effectiveness of Face-to-Face Detailing for Lemtrada
          • Lemtrada Sales Representative Frequency and Reach
            • Sales Representative Detailing Reach
            • DMT Detailing Frequency Among All Surveyed Neurologists
          • Satisfaction with Lemtrada Sales Representative
            • Satisfaction Rating for Lemtrada Sales Representative Quality Attributes
            • Qualitative Interview Follow-Ups
          • Lemtrada Message Recall
            • Topics Discussed with the Lemtrada Sales Representative*
            • Topics Discussed with the Lemtrada Sales Representative*
        • Methodology
          • Significance Testing in This Study
          • Significance Testing in This Study
        • Appendix
          • Primary Market Research
            • Years in Practice Postresidency (Percentage of Neurologists)
            • U.S. Region of Practice (Percentage of Neurologists)
            • Practice Location (Percentage of Neurologists)
            • Practice Setting (Percentage of Neurologists)
            • MS Patient Volume Under Personal Management in Past Year
            • Lemtrada REMS Program Enrollment Status
            • Enrollment Process Rating
          • Additional Information
            • Respondent Feedback
            • MS Market Background
            • DMTs Indicated for the Treatment of Relapsing Forms of MS in the United States
            • MS Market News: Lemtrada Launch
            • Objectives
            • Qualitative Interview Follow-Ups
            • DMT Treatment Rate Among RR-MS Patients
            • Likely Actions Taken Upon Lemtrada Request
            • Likely Scenario Upon Referral
            • Last Ten New DMT Prescriptions for RR-MS Patients (Percentage of DMT Prescriptions)
            • Last Ten Switch DMT Prescriptions for RR-MS Patients (Percentage of DMT Prescriptions)
            • Perception of Managed Care Approval Process Among Lemtrada Prescribers
            • Managed Care Requirements for Prescribing Lemtrada*
            • Most Common DMT Failures Requested by MCOs*
            • Percentage of Lemtrada Prescriptions Denied to…
            • Value of Genzyme’s Support Activities for Lemtrada

      Author(s): John Crowley

      John leads DRG’s Infectious, Niche, & Rare Diseases team and manages the market research portfolio across niche and rare diseases, anti-infectives, and vaccines. Prior to his current role, he was a Director on the team overseeing syndicated and custom work on niche and rare disease markets, as well as atopic dermatitis content in DRG’s Dermatology portfolio. He also served as a DRG analyst in the neurology space, focused mainly on the multiple sclerosis market. John holds a Ph.D. from the University of Massachusetts Medical School and a Bachelor’s degree from Worcester Polytechnic Institute.


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