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NCT02223832 · ClinicalTrials.gov registry record · Phase 1

Study to Evaluate the Pharmacokinetics, Tolerability, and Safety of ACT-128800 in Japanese and Caucasian Healthy Male and Female Subjects

A Phase 1 study, sponsored by Actelion.

Completed
Registry status
Phase 1
Development phase
20
Enrollment target

NCT02223832: Completed Phase 1 study, sponsored by Actelion.

NCT02223832 is a Phase 1 study that has completed, run by Actelion. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02223832, a Phase 1 study, has completed, sponsored by Actelion.

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target

Study Summary

This is a study to evaluate the relative pharmacokinetic properties and the tolerability and safety of ACT-128800 in Japanese and Caucasian healthy male and female subjects after single-dose administration.

Primary Outcome

Blood pressure shall be measured using an automatic oscillometric device, always on the leading (writing) arm. Measurements shall be taken in the supine position after having rested for at least a 5 min period.

Interventions

  • DRUG ACT-128800

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2009-02
Est. Completion 2009-04
Phase Phase 1
Actelion

63 total trials

What the finished NCT02223832 record still lists

NCT02223832 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).

The record links to 0 conditions, and to 1 intervention - of which ACT-128800 is the first listed.

NCT02223832 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02223832 about?

NCT02223832 is a clinical study titled "Study to Evaluate the Pharmacokinetics, Tolerability, and Safety of ACT-128800 in Japanese and Caucasian Healthy Male and Female Subjects". This is a study to evaluate the relative pharmacokinetic properties and the tolerability and safety of ACT-128800 in Japanese and Caucasian healthy male and female subjects after single-dose administration.

What is the current status of trial NCT02223832?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2009-02. Estimated completion is 2009-04.

What interventions are being tested in trial NCT02223832?

The interventions under investigation include: ACT-128800 (DRUG).

Who is sponsoring clinical trial NCT02223832?

This trial is sponsored by Actelion, which has 63 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02223832's enrollment target sits among peer trials

20 1629th of 2000 higher than 285 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02223832, the US trial registry maintained by the National Library of Medicine. NCT02223832 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.