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NCT01892384 · ClinicalTrials.gov registry record · Phase 1

Safety and Tolerability of BI 409306 in Patients With Schizophrenia

A Phase 1 study, sponsored by Boehringer Ingelheim.

Completed
Registry status
Phase 1
Development phase
40
Enrollment target

NCT01892384 is a Phase 1 study that has completed, run by Boehringer Ingelheim. The registered enrollment target is 40 participants.

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The verdict

NCT01892384, a Phase 1 study, has completed, sponsored by Boehringer Ingelheim.

COMPLETED
Registry status
Phase 1
Development phase
40 participants
Enrollment target

Study Summary

The primary objective of the current study is to investigate the safety and tolerability of BI 409306 in schizophrenic patients following oral administration of multiple low, medium, and high doses over 14 days. A secondary objective is the exploration of the pharmacokinetics and pharmacodynamics of BI 409306 in schizophrenic patients.

Interventions

  • DRUG Placebo
  • DRUG BI 409306

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2013-06-28
Est. Completion 2013-12-05
Phase Phase 1

Sponsor

Boehringer Ingelheim

515 total trials

What the Registry Record Tells You About NCT01892384

The ClinicalTrials.gov registry entry for NCT01892384 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boehringer Ingelheim, which has 515 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT01892384 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01892384 about?

NCT01892384 is a clinical study titled "Safety and Tolerability of BI 409306 in Patients With Schizophrenia". The primary objective of the current study is to investigate the safety and tolerability of BI 409306 in schizophrenic patients following oral administration of multiple low, medium, and high doses over 14 days. A secondary objective is the exploration of the pharmacokinetics and pharmacodynamics o...

What is the current status of trial NCT01892384?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2013-06-28. Estimated completion is 2013-12-05.

What interventions are being tested in trial NCT01892384?

The interventions under investigation include: Placebo (DRUG), BI 409306 (DRUG).

Who is sponsoring clinical trial NCT01892384?

This trial is sponsored by Boehringer Ingelheim, which has 515 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.