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NCT05245539 · ClinicalTrials.gov registry record · Phase 1

Trial to Study the Effect of CVL-231 on 24-Hour Ambulatory Blood Pressure in Participants With Schizophrenia

A Phase 1 study of Schizophrenia and Blood Pressure, sponsored by Cerevel Therapeutics.

Completed
Registry status
Phase 1
Development phase
151
Enrollment target
10
Study locations

NCT05245539 is a Phase 1 study of Schizophrenia and Blood Pressure that has completed, run by Cerevel Therapeutics. The registered enrollment target is 151 participants, below the 219-participant average among 315 other Schizophrenia trials with a reported enrollment target (31% lower). The trial reports 10 study locations across 7 states.

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The verdict

NCT05245539, a Phase 1 study of Schizophrenia and Blood Pressure, has completed, sponsored by Cerevel Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
151 participants
Enrollment target
10
Study locations

Study Summary

The purpose of this trial is to characterize the effects of 2 oral doses (over 8 weeks total) of CVL-231 on ambulatory blood pressure and heart rate in patients with stable schizophrenia.

Interventions

  • DRUG CVL-231

Study Locations (10)

Arkansas

  • Pillar Clinical Research LLC - Bentonville
  • Woodland International Research Group LLC - ERG - PPDS - Little Rock

Illinois

  • Uptown Research Institute LLC - Chicago
  • Pillar Clinical Research LLC - Lincolnwood

Texas

  • Community Clinical Research - Austin
  • Pillar Clinical Research LLC - Richardson

California

  • Collaborative NeuroScience Research, LLC - Torrance - Apex - PPDS - Long Beach

Florida

  • Innovative Clinical Research, Inc - ClinEdge - PPDS - Miami

New Jersey

  • Hassman Research Institute - Apex - PPDS - Marlton

Ohio

  • Neuro-Behavioral Clinical Research, Inc. - North Canton

Trial Details

FieldValue
Enrollment Target 151 participants
Start Date 2022-01-24
Est. Completion 2022-11-14
Phase Phase 1

Sponsor

Cerevel Therapeutics

21 total trials

What the Registry Record Tells You About NCT05245539

The ClinicalTrials.gov registry entry for NCT05245539 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 151 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 (31% lower). The listed sponsor is Cerevel Therapeutics, which has 21 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Schizophrenia appearing as the primary indexed condition, and to 1 intervention - of which CVL-231 is the first listed.

NCT05245539 reports 10 study locations spanning 7 distinct geographic areas - top geographies include Arkansas, Illinois, Texas.

Frequently Asked Questions

What is clinical trial NCT05245539 about?

NCT05245539 is a clinical study titled "Trial to Study the Effect of CVL-231 on 24-Hour Ambulatory Blood Pressure in Participants With Schizophrenia". The purpose of this trial is to characterize the effects of 2 oral doses (over 8 weeks total) of CVL-231 on ambulatory blood pressure and heart rate in patients with stable schizophrenia.

What is the current status of trial NCT05245539?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 151 participants. The study started on 2022-01-24. Estimated completion is 2022-11-14.

What conditions does trial NCT05245539 study?

This clinical trial studies the following conditions: Schizophrenia, Blood Pressure.

What interventions are being tested in trial NCT05245539?

The interventions under investigation include: CVL-231 (DRUG).

Who is sponsoring clinical trial NCT05245539?

This trial is sponsored by Cerevel Therapeutics, which has 21 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05245539 being conducted?

This trial has 10 study locations across Arkansas, California, Florida, Illinois, New Jersey. 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

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