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A Study to Assess the Relative Bioavailability of Oral Tavapadon in Healthy Adult Participants

← catalyst calendar

NCT06895356

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · None · Basic science
Enrollment
83actual
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-03-26actualWhen the study began enrolling
Primary completion2025-06-16actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-06-16actualThe whole study's end, after follow-up
First posted2025-03-26actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-06-26actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Volunteer

Intervention

  • Drug: Tavapadon

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants Experiencing Adverse Events
measured Up to approximately 53 days
Maximum Observed Plasma Concentration (Cmax) of Tavapadon
measured Up to approximately 22 days
Time to Cmax (Tmax) of Tavapadon
measured Up to approximately 22 days
Apparent Terminal Phase Elimination Rate Constant (β) of Tavapadon
measured Up to approximately 22 days
Terminal Phase Elimination Half-life (t1/2) of Tavapadon
measured Up to approximately 22 days
Area Under the Plasma Concentration-time Curve Over the Dosing Interval (AUCτ) of Tavapadon
measured Up to approximately 22 days
Area Under the Plasma Concentration-time Curve from Time Zero to Infinity (AUCinf) of Tavapadon
measured Up to approximately 22 days
Trough Concentration (Ctrough) of Tavapadon
measured Up to approximately 22 days

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