Adherence to Treatment With Tecfidera™ in Multiple Sclerosis Patients

Completed

Conditions studied: Multiple Sclerosis

In brief

The investigators are measuring the adherence rates of an oral MS drug that is to be administered twice-daily. The investigators would like to observe any patterns that might indicate factors that greatly affect adherence.

Key facts

Study ID

NCT02099370

Run by

University of South Florida

People needed

34

Starts

2014-03-01

Expected to finish

2016-01-01

Last updated by the study team

2020-04-03

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Must give written informed consent and any authorizations required by local law (e.g., Protected Health Information [PHI]).
• Aged 18 at the time of informed consent.
• Must have a relapsing form of MS.
• Male subjects and female subjects of child-bearing potential (including female subjects who are not post-menopausal for at least 1 year) must be willing to practice effective contraception (as defined by the investigator) during the study and be willing and able to continue contraception for 30 days after their last dose of study treatment.

You may not qualify if…

• Progressive form of MS
• History of severe allergic or anaphylactic reactions or known drug hypersensitivity.
• Female subjects considering becoming pregnant while in the study.
• Female subjects who are currently pregnant or breast-feeding.
• Unwillingness or inability to comply with the requirements of the protocol including the presence of any conditional (physical, mental or social) that is likely to affect the subject's ability to comply with the protocol.
• Any other reason that, in opinion of the Investigator and/or the Sponsor, the subject is determined to be unsuitable for enrollment in this study.

Where it is running

• USF Carol and Frank Morsani Center for Advanced Healthcare — Tampa, Florida, United States

Full record on ClinicalTrials.gov

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