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Dosing and administration

MAVENCLAD™ HAS A WEIGHT-BASED DOSING REGIMEN1

MAVENCLAD is administered as one treatment course per year over 2 years, followed by observation for another 2 years. Each treatment course consists of 2 treatment weeks: week 1 and week 5.1

Dosing Guide

This dosing tool will display the correct MAVENCLAD dose by patient weight per treatment year.

Please enter your patient's weight:
Please only enter numbers up to one decimal place

WEEK 1
pill pill
WEEK 5
Day 1 0 0 Day 1
Day 2 0 0 Day 2
Day 3 0 0 Day 3
Day 4 0 0 Day 4
Day 5 0 0 Day 5
Total Tablets
0
0
0
0
0
0

Use of MAVENCLAD in patients weighing less than 40 kg has not been investigated. Please enter a value ≥40 kg.

Full Dosing Table

Dosing Table

Learn more about MAVENCLAD

 

Demonstrated efficacy

Monitoring

Safety and tolerability profile

  

 

Explore MAVENCLAD’s efficacy.

Learn more

Discover MAVENCLAD’s monitoring.

Learn more

Learn about MAVENCLAD’s safety and
tolerability profile.

Learn more

  
Footnotes and References

  1. MAVENCLAD™ Product Monograph. EMD Serono. November 2017.
  2. Giovannoni G, et al. A placebo-controlled trial of oral cladribine for relapsing multiple sclerosis. N Engl J Med 2010;362:416-26.

© 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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