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NCT00361790 · ClinicalTrials.gov registry record · Phase 1

Aripiprazole and Lexapro Drug Interaction Study

A Phase 1 study, sponsored by Otsuka Pharmaceutical Development & Commercialization.

Completed
Registry status
Phase 1
Development phase
25
Enrollment target

NCT00361790 is a Phase 1 study that has completed, run by Otsuka Pharmaceutical Development & Commercialization. The registered enrollment target is 25 participants.

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The verdict

NCT00361790, a Phase 1 study, has completed, sponsored by Otsuka Pharmaceutical Development & Commercialization.

COMPLETED
Registry status
Phase 1
Development phase
25 participants
Enrollment target

Study Summary

The purpose of this clinical research study is to learn whether aripiprazole has effect on the steady-state pharmacokinetics of escitalopram in healthy subjects. The safety and tolerability of aripiprazole and escitalopram co-administration will also be studied.

Interventions

  • DRUG Escitalopram on days -7 to day 14; Aripiprazole dosed starting Day 1 to day 14: 3 days at 10 mg, 4 days at 15 mg and 7 days at 20 mg

Trial Details

FieldValue
Enrollment Target 25 participants
Start Date 2006-08
Est. Completion 2006-11
Phase Phase 1

What the Registry Record Tells You About NCT00361790

The ClinicalTrials.gov registry entry for NCT00361790 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Otsuka Pharmaceutical Development & Commercialization, which has 221 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Escitalopram on days -7 to day 14; Aripiprazole dosed starting Day 1 to day 14: 3 days at 10 mg, 4 days at 15 mg and 7 days at 20 mg is the first listed.

NCT00361790 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00361790 about?

NCT00361790 is a clinical study titled "Aripiprazole and Lexapro Drug Interaction Study". The purpose of this clinical research study is to learn whether aripiprazole has effect on the steady-state pharmacokinetics of escitalopram in healthy subjects. The safety and tolerability of aripiprazole and escitalopram co-administration will also be studied.

What is the current status of trial NCT00361790?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 25 participants. The study started on 2006-08. Estimated completion is 2006-11.

What interventions are being tested in trial NCT00361790?

The interventions under investigation include: Escitalopram on days -7 to day 14; Aripiprazole dosed starting Day 1 to day 14: 3 days at 10 mg, 4 days at 15 mg and 7 days at 20 mg (DRUG).

Who is sponsoring clinical trial NCT00361790?

This trial is sponsored by Otsuka Pharmaceutical Development & Commercialization, which has 221 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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