A Trial of 10 and 30 mg Doses of CVL-231 (Emraclidine) in Participants With Schizophrenia
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| ClinicalTrials.gov Identifier: NCT05227690 |
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Recruitment Status :
Recruiting
First Posted : February 7, 2022
Last Update Posted : February 17, 2023
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Sponsor:
Cerevel Therapeutics, LLC
Information provided by (Responsible Party):
Cerevel Therapeutics, LLC
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Brief Summary:
This is a Phase 2, multicenter, randomized, double-blind, placebo-controlled, parallel-group, 6-week trial to evaluate the efficacy, safety, and tolerability of 2 fixed doses of CVL-231 (Emraclidine) (10 mg QD and 30 mg QD) in male and female participants who have schizophrenia and are experiencing an acute exacerbation of psychosis.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Schizophrenia | Drug: CVL-231 10 mg Drug: Required CVL-231 30 mg Drug: Placebo | Phase 2 |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 372 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Intervention Model Description: | Placebo-controlled |
| Masking: | Double (Participant, Investigator) |
| Primary Purpose: | Treatment |
| Official Title: | A Phase 2, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Efficacy, Safety, and Tolerability of Two Fixed Doses (10 mg and 30 mg QD) of CVL-231 (Emraclidine) in Participants With Schizophrenia Experiencing an Acute Exacerbation of Psychosis |
| Actual Study Start Date : | June 30, 2022 |
| Estimated Primary Completion Date : | May 2024 |
| Estimated Study Completion Date : | June 2024 |
Resource links provided by the National Library of Medicine
MedlinePlus Genetics related topics:
Schizophrenia
| Arm | Intervention/treatment |
|---|---|
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Experimental: CVL-231 10 mg, once daily (QD)
Oral Dose
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Drug: CVL-231 10 mg
CVL-231 10 mg, oral (tablet), once per day for 6 weeks |
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Experimental: CVL-231 30 mg, once daily (QD)
Oral Dose
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Drug: Required CVL-231 30 mg
CVL-231 30 mg, oral (tablet), once per day for 6 weeks |
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Placebo Comparator: Placebo, once daily (QD)
Oral Dose
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Drug: Placebo
Matching placebo, oral (tablet), once per day for 6 weeks |
Primary Outcome Measures :
- Change from Baseline at Week 6 in the Positive and Negative Syndrome Scale (PANSS) total score [ Time Frame: Baseline through Week 6 ]The PANSS measures symptom severity of participants with schizophrenia and contains 7 positive symptom scales, 7 negative system scales, and 16 general psychopathology symptom scales. Participants are rated from 1 to 7 on each symptom scale with a total minimum score of 30 and a maximum score of 210. A decrease in PANSS total score correlates with an improvement in schizophrenia symptoms.
Secondary Outcome Measures :
- Change from Baseline at Week 6 in the Clinical Global Impression - Severity (CGI-S score) [ Time Frame: Baseline through Week 6 ]The CGI-S captures clinician's response to: "Considering your total clinical experience, how mentally ill is the participant at this time?" The clinician's answer rated on the following 7-point scale: 1 = normal, not at all ill; 2 = borderline mentally ill; 3 = mildly ill; 4 = moderately ill; 5 = markedly ill; 6 = severely ill; 7 = among the most extremely ill participants.
- Change from Baseline at all time points in Positive and Negative Syndrome Scale (PANSS) total score [ Time Frame: Baseline through Week 6 ]The PANSS measures symptom severity of participants with schizophrenia and contains 7 positive symptom scales, 7 negative system scales, and 16 general psychopathology symptom scales. Participants are rated from 1 to 7 on each symptom scale with a total minimum score of 30 and a maximum score of 210. A decrease in PANSS total score correlates with an improvement in schizophrenia symptoms.
- Change from Baseline at all time points in the Clinical Global Impression - Severity (CGI-S) score [ Time Frame: Baseline through Week 6 ]The CGI-S captures clinician's response to: "Considering your total clinical experience, how mentally ill is the participant at this time?" The clinician's answer rated on the following 7-point scale: 1 = normal, not at all ill; 2 = borderline mentally ill; 3 = mildly ill; 4 = moderately ill; 5 = markedly ill; 6 = severely ill; 7 = among the most extremely ill participants.
- Percentage of responders at Week 6 (responders defined as ≥30% reduction from Baseline in PANSS total score) [ Time Frame: Baseline through Week 6 ]A PANSS responder is defined as a participant with at least a 30% change in PANSS total score compared to baseline at Week 6.
- Incidence and Severity of Treatment Emergent Adverse Events (TEAEs) [ Time Frame: Up to Week 10 ]Any AE occurring following the start of treatment or occurring before treatment but increasing in severity afterward will be counted as treatment-emergent AE (TEAE)
- Incidence of clinically significant changes in electrocardiogram (ECG) results [ Time Frame: Up to Week 6 ]Assessment of clinically significant changes in electrocardiogram measures measured by 12-lead ECG recording after the participant has been supine and at rest for at least 3 minutes
- Incidence of clinically significant changes in clinical laboratory results [ Time Frame: Up to Week 6 ]
- Incidence of clinically significant changes in vital sign measurements [ Time Frame: Up to Week 6 ]Assessment of clinically significant changes in vital signs including temperature, systolic and diastolic blood pressure, and heart rate.
- Incidence of clinically significant changes in physical and neurological examination results [ Time Frame: Up to Week 6 ]
- Clinically significant findings in suicidality assessed using the Columbia Suicide-Severity Rating Scale (C-SSRS) [ Time Frame: Up to Week 6 ]The C-SSRS rates an individual's degree of suicidal ideation (SI) on a scale, ranging from "wish to be dead" to "active suicidal ideation with specific plan and intent." The scale identifies SI severity and intensity, which may be indicative of an individual's intent to commit suicide. C-SSRS SI severity subscale ranges from 0 (no SI) to 5 (active SI with plan and intent).
- Frequency of clinically significant findings in extrapyramidal symptoms evaluated using the Simpson Angus Scale (SAS) [ Time Frame: Up to Week 6 ]The SAS consists of a list of 10 symptoms of parkinsonism. Each item is rated on a 5-point scale, with a score of 0 representing absence of symptoms and a score of 4 representing a severe condition. The SAS total score is the sum of the scores for all 10 items.
- Frequency of clinically significant findings in extrapyramidal symptoms evaluated using the Barnes Akathisia Rating Scale (BARS) [ Time Frame: Up to Week 6 ]The BARS consists of 4 items related to akathisia: The first 3 items are rated on a 4-point scale, with a score of 0 representing absence of symptoms and a score of 3 representing a severe condition. The global clinical evaluation is made on a 6-point scale, with a score of 0 representing absence of symptom and a score of 5 representing severe akathisia.
- Frequency of clinically significant findings in extrapyramidal symptoms evaluated using the Abnormal Involuntary Movement Scale (AIMS) [ Time Frame: Up to Week 6 ]The AIMS assessment consists of 10 items describing symptoms of dyskinesia. Each item is rated on a 5-point scale, with a score of 0 representing absence of symptoms (for item 10, no awareness), and a score of 4 indicating a severe condition (for item 10, awareness, severe distress). In addition, the AIMS includes 2 yes/no questions that address the subject's dental status.
Other Outcome Measures:
- Clinical Global Impression - Improvement (CGI-I) score at Weeks 3 and 6 [ Time Frame: Time Frame: Week 3 and Week 6 ]The CGI-I captures clinician's response to: "Rate total improvement whether or not, in your judgment, it is due entirely to drug treatment. Compared to his/her condition at admission to the project (screening) how much has he /she changed? 0 = Not assessed 1 = Very much improved 2 = Much improved 3 = Minimally improved 4 = No change 5 = Minimally worse 6 = Much worse 7 = Very much worse
- Change from Baseline at all time points in Positive and Negative Syndrome Scale (PANSS) positive, negative, and general psychopathology subscale scores [ Time Frame: Every week from baseline through Week 6 ]The PANSS measures symptom severity of participants with schizophrenia and contains 7 positive symptom scales, 7 negative system scales, and 16 general psychopathology symptom scales. Participants are rated from 1 to 7 on each symptom scale with a total minimum score of 30 and a maximum score of 210. A decrease in PANSS total score correlates with an improvement in schizophrenia symptoms.
- Change from Baseline at all time points in PANSS Marder Factor scores Change from Baseline at all time points in PANSS Marder Factor scores Change from Baseline at all time points in PANSS Marder Factor scores [ Time Frame: Every week from baseline through Week 6 ]The Negative Marder Factor score is calculated as the sum of the rating assigned to each of the 7 applicable Marder factor items, and ranges from 7 to 49 with a higher score indicating greater severity of symptoms.
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| Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Primary diagnosis of schizophrenia per DSM-5, as confirmed by the MINI for Psychotic Disorders.
- CGI-S ≥4 (moderately to severely ill) at the time of signing the ICF and Baseline.
- PANSS Total Score between 85 and 120, inclusive, at the time of signing the ICF and at Baseline.
- Experiencing an acute exacerbation or relapse of psychotic symptoms, with onset less than 60 days prior to signing the ICF.
- Willing to discontinue all prohibited medications to meet protocol-required washouts prior to and during the trial period.
- Body mass index of 18.0 to 40.0 kg/m2 and a total body weight ≥50 kg (110 lbs).
- Ability, in the opinion of the investigator, to understand the nature of the trial, participate in trial visits, and comply with protocol requirements.
Exclusion Criteria:
- Current DSM-5 diagnosis other than schizophrenia (note: anxiety symptoms secondary to schizophrenia are allowed); Acute depressive symptoms within 30 days prior to signing the ICF that require treatment with an antidepressant are exclusory. Acute manic symptoms within 30 days prior to signing the ICF that require treatment with a mood stabilizer are exclusory.
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Any of the following:
- Schizophrenia considered resistant/refractory to antipsychotic treatment by history (failure to respond to 2 or more courses of adequate pharmacological treatment defined as an adequate dose per label and a treatment duration of at least 4 weeks)
- History of response to clozapine treatment only or failure to respond to clozapine treatment
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Any of the following regarding history of schizophrenia:
- Time from initial onset of schizophrenia <2 years based on prior records or participant self-report
- Presenting with an initial diagnosis of schizophrenia
- Presenting for the first time with an acute psychotic episode requiring treatment
- Reduction (improvement) in PANSS total score of ≥20% between Screening and Baseline.
- Current or past history of significant cardiovascular, pulmonary, gastrointestinal, renal, hepatic, metabolic, genitourinary, endocrine (including diabetes mellitus), malignancy (except for basal cell carcinoma of the skin and cervical carcinoma in situ, at the discretion of the investigator), hematological, immunological, neurological, or psychiatric disease that, in the opinion of the investigator or medical monitor, could compromise either participant safety or the results of the trial.
- Active central nervous system infection, demyelinating disease, degenerative neurological disease, brain tumor, prior hospitalization for severe head trauma, seizures (excluding febrile seizures in childhood), or any central nervous system disease deemed to be progressive during the course of the trial that may confound the interpretation of the trial results
- Diagnosis of moderate to severe substance or alcohol-use disorder (excluding nicotine or caffeine) as per DSM-5 criteria within 12 months prior to signing the ICF.
- Risk for suicidal behavior as assessed by the Columbia-Suicide Severity Rating Scale (C-SSRS) and investigator's clinical assessment.
- Any condition that could possibly affect drug absorption.
- Use of prohibited medications prior to randomization within the required wash-out period or likely to require prohibited concomitant therapy during the trial.
- Clinically significant abnormal findings on the physical examination, medical history review, ECG, or clinical laboratory results at screening.
- Positive pregnancy test result prior to receiving IMP. Note: female participants who are pregnant, breastfeeding, or planning to become pregnant during IMP treatment or within 7 days after the last dose of IMP are also excluded.
Information from the National Library of Medicine
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05227690
Locations
Show 17 study locations
Sponsors and Collaborators
Cerevel Therapeutics, LLC
Investigators
| Study Director: | Erica Koenig, PhD | Cerevel Therapeutics, LLC |
| Responsible Party: | Cerevel Therapeutics, LLC |
| ClinicalTrials.gov Identifier: | NCT05227690 |
| Other Study ID Numbers: |
CVL-231-2001 |
| First Posted: | February 7, 2022 Key Record Dates |
| Last Update Posted: | February 17, 2023 |
| Last Verified: | February 2023 |
| Studies a U.S. FDA-regulated Drug Product: | Yes |
| Studies a U.S. FDA-regulated Device Product: | No |
Keywords provided by Cerevel Therapeutics, LLC:
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Schizophrenia Schizophrenia Spectrum and Other Psychotic Disorders Mental Disorders |
Additional relevant MeSH terms:
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Schizophrenia Schizophrenia Spectrum and Other Psychotic Disorders Mental Disorders |