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Patient experience

MAVENCLAD™ IS SUPPORTED BY 4 YEARS OF CLINICAL TRIAL EXPERIENCE AND UP TO 8 YEARS OF FOLLOW-UP EXPERIENCE WITH OVER 10,000 PATIENT-YEARS1

Timeline

Learn more about MAVENCLAD

 

Demonstrated efficacy

MOA

Safety and tolerability profile

  

 

Explore MAVENCLAD’s efficacy.

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Understand MAVENCLAD’s MOA.

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Learn about MAVENCLAD’s safety
and tolerability profile.

Learn more

  
Footnotes and References

RRMS=relapsing-remitting multiple sclerosis

  1. Letter on file. EMD Serono. December 2017.
  2. MAVENCLAD™ Product Monograph. EMD Serono. November 2017.
  3. Giovannoni G, et al. Safety and efficacy of cladribine tablets in patients with relapsing-remitting multiple sclerosis: results from the randomized extension trial of the CLARITY study. Mult Scler 2017 [Epub ahead of print].

© 2019 EMD Serono. All rights reserved.
MAVENCLAD™ is a trademark of Merck KGaA, Darmstadt, Germany.

Importer & Distributor:
EMD Serono, A Division of EMD Inc., Canada
A business of Merck KGaA, Darmstadt, Germany
2695 North Sheridan Way, Suite 200
Mississauga, Ontario  L5K 2N6 Canada

If your patients experience any side effects, they should talk to their doctor, pharmacist or nurse. This includes any possible side effects not listed in the package insert. Side effects can also be reported directly via the Health Canada website at www.healthcanada.gc.ca/medeffect, by calling the Regional Adverse Reaction Centre at 1-866-234-2345 or by contacting the adveva team at 1-888-677-3243.

CA/CLA/0318/0013E

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