Absolute Bioavailability of a Single, Fixed Subcutaneous Dose of Aducanumab in Healthy Participants
Completed · Phase 1
Conditions studied: Alzheimer's Disease
In brief
The primary objectives of this study are to evaluate the absolute bioavailability of a single, fixed sub-cutaneous (SC) dose of aducanumab compared with a single, weight-based intra-venous (IV) dose in healthy participants and to characterize the pharmacokinetics (PK) profile of aducanumab. The secondary objectives are to evaluate the safety and tolerability of aducanumab administered via SC and IV routes in healthy participants and to characterize additional PK parameters of a single, fixed SC dose of aducanumab and a weight-based IV dose in healthy participants.
Key facts
- Study ID
- NCT02782975
- Run by
- Biogen
- People needed
- 28
- Starts
- 2016-05-01
- Expected to finish
- 2016-11-01
- Last updated by the study team
- 2017-01-13
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
Where it is running
- Research Site — Evansville, Indiana, United States
- Research Site — Dallas, Texas, United States
Full record on ClinicalTrials.gov
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