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NCT02202226 · ClinicalTrials.gov registry record · Phase 1

Safety and Tolerability Study of Lu AF35700 After Repeated Dosing in Patients With Schizophrenia

A Phase 1 study of Schizophrenia, sponsored by H. Lundbeck A/S.

Completed
Registry status
Phase 1
Development phase
96
Enrollment target
1
Study location

NCT02202226 is a Phase 1 study of Schizophrenia that has completed, run by H. Lundbeck A/S. The registered enrollment target is 96 participants, below the 219-participant average among 315 other Schizophrenia trials with a reported enrollment target (56% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02202226, a Phase 1 study of Schizophrenia, has completed, sponsored by H. Lundbeck A/S.

COMPLETED
Registry status
Phase 1
Development phase
96 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the tolerability and safety of Lu AF35700 after repeated oral dosing to patients with schizophrenia.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Lu AF35700

Study Locations (1)

California

  • PAREXEL Phase I Unit - Glendale

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 2013-01
Phase Phase 1

Sponsor

H. Lundbeck A/S

72 total trials

What the Registry Record Tells You About NCT02202226

The ClinicalTrials.gov registry entry for NCT02202226 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 96 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 219-participant average among 315 other Schizophrenia trials with a reported enrollment target (56% lower). The listed sponsor is H. Lundbeck A/S, which has 72 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Schizophrenia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT02202226 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT02202226 about?

NCT02202226 is a clinical study titled "Safety and Tolerability Study of Lu AF35700 After Repeated Dosing in Patients With Schizophrenia". The purpose of this study is to evaluate the tolerability and safety of Lu AF35700 after repeated oral dosing to patients with schizophrenia.

What is the current status of trial NCT02202226?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 96 participants. The study started on 2013-01.

What conditions does trial NCT02202226 study?

This clinical trial studies the following conditions: Schizophrenia.

What interventions are being tested in trial NCT02202226?

The interventions under investigation include: Placebo (DRUG), Lu AF35700 (DRUG).

Who is sponsoring clinical trial NCT02202226?

This trial is sponsored by H. Lundbeck A/S, which has 72 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02202226 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.