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Unknown
CVL-231 for High Blood Pressure
Phase 1
Waitlist Available
Research Sponsored by Cerevel Therapeutics, LLC
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline through day 84
Awards & highlights
Study Summary
This trial is testing a new medication to see if it lowers blood pressure and heart rate in people with stable schizophrenia.
Eligible Conditions
- High Blood Pressure
- Schizophrenia
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline through day 84
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline through day 84
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Mean change from Baseline to Week 8 in the 24-hour ambulatory SBP (Systolic Blood Pressure)
Secondary outcome measures
Area under the plasma concentration-time curve over dosing interval (AUCτ) for CVL-231 and Metabolite (PF-06892787)
Frequency of clinically significant changes in clinical laboratory assessments
Frequency of clinically significant changes in electrocardiograms
+14 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: CVL-231 Dose Level 2Experimental Treatment1 Intervention
30 mg once daily
Group II: CVL-231 Dose Level 1Experimental Treatment1 Intervention
10 mg once daily
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
CVL-231
2022
Completed Phase 1
~300
Find a Location
Who is running the clinical trial?
Cerevel Therapeutics, LLCLead Sponsor
34 Previous Clinical Trials
5,544 Total Patients Enrolled
Erica Koenig, PhDStudy DirectorCerevel Therapeutics, LLC
3 Previous Clinical Trials
1,594 Total Patients Enrolled
Frequently Asked Questions
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