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Muscarinic Receptor Antagonist
CVL-231 for Schizophrenia
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 day 1 (0.5, 1.5 and 2.0 hours)
Awards & highlights
No Placebo-Only Group
Summary
This trial studies how CVL-231, a drug targeting brain receptors, works in healthy adults. The goal is to understand its effects on specific brain areas before using it to treat schizophrenia.
Eligible Conditions
- Schizophrenia
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ day 1 (0.5, 1.5 and 2.0 hours)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 1 (0.5, 1.5 and 2.0 hours)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
M4 receptor occupancy in the striatum following single oral doses of CVL-231 in healthy adult subjects
Secondary study objectives
AUCscan duration for CVL-231
Cavg/Scan duration for CVL-231
Cmax during scan for CVL-231
+2 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: CVL-231Experimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
CVL-231
2022
Completed Phase 1
~300
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
Cerevel Therapeutics, LLCLead Sponsor
36 Previous Clinical Trials
5,692 Total Patients Enrolled
7 Trials studying Schizophrenia
2,011 Patients Enrolled for Schizophrenia
Matthew Leoni, MD, MBAStudy DirectorCerevel Therapeutics, LLC
2 Previous Clinical Trials
89 Total Patients Enrolled
1 Trials studying Schizophrenia
16 Patients Enrolled for Schizophrenia
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