InCROM Clinical Research Unit
London, E14NL, United Kingdom
NCT Number: NCT01017666
The purpose of this study is to understand whether BIIB014 has potential to affect how certain drugs are broken down by the body.
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Notify Me18 year–45 year
All sexes
Interventional
Phase 1
London, E14NL, United Kingdom
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
BIIB014 100mg PO Cohort 1 - 8d Cohort 2 - 14d
Matched placebo to BIIB014 Cohort 1 - 8d Cohort 2 - 14d
Time frame: 24 hours (Cohort 1); 144 hours (Cohort 2)
Time frame: Duration of subject participation
Biogen
Industry
A Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Assess the Effect of BIIB014 on the Pharmacokinetics of Rosiglitazone, Warfarin, and Midazolam in Healthy Volunteers
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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