NCT02343159Study to Evaluate Whether a Medication Event Monitoring System (MEMS) Can Improve Adherence to Tecfidera Treatment in Multiple Sclerosis Patients.
Please note, some trial-specific information on this page is sourced from clinicaltrials.gov.
About
Trial summary
TYPEINTERVENTIONAL
PHASE
Phase
Clinical trials are done in different phases (0-4). Each phase provides important information about the drug. If a drug does not pass a particular phase, it cannot progress to the next phase. Visit the About Clinical Trials page to learn more.
PHASE4
CONDITION
Multiple Sclerosis
INTERVENTIONS
Interventions
The drug, device, or procedure being tested.
DRUG:dimethyl fumarate
120 mg and 240 mg delayed release capsules
DEVICE:Medication Event Monitoring System (MEMS)
The MEMS automatically compiles drug dosing history data by electronically recording the date and time of each opening of the medication container
BEHAVIORAL:Adherence counseling
A telephone call to discuss adherence and individualized strategies based on data collected via smart device (i.e., LCD reader)
ENROLLMENT
Enrollment
The number of participants needed to take part in this trial.
84 participants
(ACTUAL)
18 Years to 65 Years
(ADULT, OLDER ADULT)
LOCATIONS29
Key dates
Key dates
When the trial is conducted - from the date the first participant is enrolled to the date of the last participants's final visit.
Results from this trial have been made available. Some information may be redacted (edited) to protect privacy, publication rights, and confidential commercial information. To review the information please visit biogentrialtransparency.com.
PDF
Clinical trial registers
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Please contact a clinical trial site directly to learn more about the trial. If no contact details are available, or for general inquiries, please contact the Biogen Clinical Trial Center.
