Trial to Investigate the Safety and Efficacy of GWP42003-P Versus Placebo as Adjunctive Therapy in Participants With Schizophrenia Experiencing Inadequate Response to Ongoing Antipsychotic Treatment

Schizophrenia Clinical Trial

Official title:

A Randomized, Double-blind, Parallel-group Trial to Investigate the Safety and Efficacy of GWP42003-P Versus Placebo as Adjunctive Therapy in Participants With Schizophrenia Experiencing Inadequate Response to Ongoing Antipsychotic Treatment

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT04421456
• Other study ID #: GWAP19030
• Secondary ID: 2019-003369-16
• Status: Terminated
• Phase: Phase 2
• Start date: August 18, 2020
• Est. completion date: March 16, 2022

Study information

• Verified date: June 2023
• Source: Jazz Pharmaceuticals
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will be conducted to evaluate the efficacy, safety, and tolerability of GWP42003-P versus placebo in participants with schizophrenia experiencing inadequate response to ongoing antipsychotic treatment.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 95
• Est. completion date: March 16, 2022
• Est. primary completion date: March 16, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Male or female 18 to 55 years of age at the time of signing the Informed Consent Form (ICF)

• Willing and able to give informed consent for participation in the trial

• Diagnostic and Statistical Manual of Mental Disorders (DSM-5) diagnosis of schizophrenia, confirmed by the Mini International Neuropsychiatric Interview (MINI)

• Clinically stable outpatient

• Positive and Negative Symptoms Scale (PANSS) Total (PANSS-T) score of = 60 and < 110 at screening and baseline visits

• Score of = 4 for at least 2 of the following PANSS items: delusions (P1), conceptual disorganization (P2), hallucinatory behavior (P3), suspiciousness (P6), somatic concern (G1), or unusual thought content (G9) at screening visit

• Score = 4 (at least moderately ill) on the Clinical Global Impression of Severity (CGI-S) at screening visit.

• Undergoing treatment with at least 1 antipsychotic medication with no change in dosing, supported by documentation, for at least 8 weeks prior to screening and no change in antipsychotic medication dosing planned throughout the trial

• Taking a maximum of 2 antipsychotic medications. For participants taking oral antipsychotic medications only, the sum of primary and secondary antipsychotic medications is = 30 milligrams (mg)/day of oral olanzapine equivalents. For participants taking long-acting injectable antipsychotic medications, the dose is within the range approved and any secondary oral antipsychotic medications is = 5 mg/day of oral olanzapine equivalents.

• Documented response (at least partially) to treatment with current antipsychotic medications (e.g., treatment of recent exacerbation of psychotic symptoms)

• On a stable dose if taking concomitant psychotropic medications and within allowed limits, including antidepressants, anxiolytics, anticholinergics and/or antiepileptics for at least 4 weeks prior to screening (dose reductions = 25% of total dose are permitted) with no plans to change dosing during the trial (i.e., from screening onwards). Valproic acid or any prescribed valproate product (valproate semisodium or valproate sodium) is disallowed within 4 weeks (i.e., more than 5 half lives) prior to the baseline visit.

Exclusion Criteria:

Diagnosis and Psychiatric History

• Recent (within the last 3 months prior to screening) diagnosis of panic disorder, depressive episode, or other comorbid psychiatric conditions based on the MINI for Psychotic Disorders Studies (or DSM-5) OR has PANSS item G6 score of = 5 (depression) at screening.

• Any psychiatric disorder that may interfere with the conduct of this trial, including but not limited to attention deficit hyperactivity disorder, pervasive developmental disorder, intellectual disability, personality disorder that might interfere with compliance or increase suicidal risk, manic or hypomanic episode, or any other psychotic disorder, as defined in the DSM-5

• Current diagnosis or a history of substance use disorder according to DSM-5 criteria within 6 months prior to screening or prior chronic substance abuse judged likely to recur during the trial period by the investigator. Nicotine use or occasional cannabis use (= 3 days per week recreational cannabis use) is acceptable. Corroboration of the participant's frequency of cannabis use by an adult informant (e.g., family member, social worker, caseworker, residential facility staff, or nurse), should be obtained if the participant has a positive urine test for ?9-tetrahydrocannabinol at screening.

• A positive drug screen for opiates, methadone, cocaine, amphetamines (including ecstasy), or barbiturates; a repeat drug screen may be done to verify the result.

• Any history of suicidal behavior or any suicidal ideation of type 4 or 5 on the adult C-SSRS or within 1 month prior to screening

Treatment History

• Treatment-resistant schizophrenia as judged by the treating physician and as defined by having previously demonstrated no response to > 2 trials of antipsychotic trial medications at therapeutic doses or required clozapine therapy due to non-response to antipsychotic therapy within the previous 6 months.

• Based on the investigator assessment, current antipsychotic medication blood levels are below the therapeutic range if therapeutic drug monitoring is available for the antipsychotic(s) prescribed for the participant; or there is no documentation confirming the administration of long-acting injectable antipsychotic medication within the approved dose range and as prescribed by the treating physician.

Past and Current Medical History

• History of moderate or severe head trauma (for example, loss of consciousness for more than 15 minutes) or other neurological disorders (including epilepsy), neurodegenerative disorder (Alzheimer's disease, Parkinson's disease, multiple sclerosis, Huntington's disease, etc.) or systemic medical diseases that are, in the opinion of the investigator, likely to interfere with the conduct of the trial or confound the trial assessments

• Tardive dyskinesia (TD) that is moderate to severe (i.e., a score of > 21 on the dyskinesia subscale of the Extrapyramidal Symptom Rating Scale [ESRS] at screening) or requires treatment

• Any other significant disease, disorder, pending court proceedings or social circumstances which, in the opinion of the investigator, may either put the participant at risk because of participation in the trial, may influence the result of the trial, or may affect the participant's ability to take part in the trial.

Other

• Any known or suspected hypersensitivity to cannabinoids or any of the excipients of the investigational medicinal product, such as sesame seed oil

• One or more laboratory values outside the normal range, based on the blood or urine samples taken at the screening visit, that are considered by the investigator to be clinically significant; or impaired hepatic function at screening, defined as serum alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2 × upper limit of normal (ULN) or total bilirubin (TBL) > 1.5 × ULN or international normalized ratio (INR) > 1.2 (TBL ULN parameter not applicable for participants diagnosed with Gilbert's disease)

• Currently using or within 3 months of screening has used cannabidiol (CBD) oil or purified CBD preparations and is unwilling to abstain for the duration of the trial

Related Conditions & MeSH terms

• Schizophrenia

Intervention

Drug:
• GWP42003-P
oral solution containing 100 milligrams per milliliter (mg/mL) cannabidiol (CBD) dissolved in the excipients sesame oil and anhydrous ethanol (10% v/v), with sweetener (sucralose), and strawberry flavoring
• Placebo
oral solution containing the excipients sesame oil and anhydrous ethanol, with added ß-carotene, sweetener (sucralose), and strawberry flavoring

Locations

Country	Name	City	State
Poland	Clinical Trial Site	Belchatow
Poland	Clinical Trial Site	Gdansk
Poland	Clinical Trial Site	Kielce
Poland	Clinical Trial Site	Kobierzyce
Poland	Clinical Trial Site	Poznan
Poland	Clinical Trial Site	Torun
Poland	Clinical Trial Site	Wroclaw
Poland	Clinical Trial Site	Wroclaw
Serbia	Clinical Trial Site#1	Belgrade
Serbia	Clinical Trial Site#2	Belgrade
Serbia	Clinical Trial Site#1	Kovin
Serbia	Clinical Trial Site#2	Kovin
Serbia	Clinical Trial Site#1	Kragujevac
Serbia	Clinical Trial Site#2	Kragujevac
Serbia	Clinical Trial Site#3	Kragujevac
Serbia	Clinical Trial Site	Nis
Spain	Clinical Trial Site	Barcelona
Spain	Clinical Trial Site	Oviedo
Spain	Clinical Trial Site	Salamanca
Spain	Clinical Trial Site	Valladolid
United States	Clinical Trial Site	Beachwood	Ohio
United States	Clinical Trial Site	Bentonville	Arkansas
United States	Clinical Trial Site	Berlin	New Jersey
United States	Clinical Trial Site	Cedarhurst	New York
United States	Clinical Trial Site	Garden Grove	California
United States	Clinical Trial Site	Largo	Florida
United States	Clinical Trial Site	Las Vegas	Nevada
United States	Clinical Trial Site	Lauderhill	Florida
United States	Clinical Trial Site	Lemon Grove	California
United States	Clinical Trial Site	Lincolnwood	Illinois
United States	Clinical Trial Site	Little Rock	Arkansas
United States	Clinical Trial Site	New York	New York
United States	Clinical Trial Site	Oakland	California
United States	Clinical Trial Site	Pico Rivera	California
United States	Clinical Trial Site	Richardson	Texas
United States	Clinical Trial Site	Rochester	New York
United States	Clinical Trial Site	Saint Louis	Missouri
United States	Clinical Trial Site	Shreveport	Louisiana
United States	Clinical Trial Site	Tampa	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Jazz Pharmaceuticals

Countries where clinical trial is conducted

United States,  Poland,  Serbia,  Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Least Square Mean Change From Baseline in the Positive and Negative Symptoms Scale (PANSS) Total (PANSS-T) Score	The PANSS-T is a medical scale used for measuring symptom severity of participants with schizophrenia or related psychotic disorder. It is a 30-item rating instrument that assesses the positive and negative symptoms of schizophrenia as well as symptoms of general psychopathology. Individual items are rated on a 7-point scale, where 1 = absent and 7 = extreme. A PANSS-T score is derived from the sum of the 30 items and the total score ranges from 30 to 210, where higher scores represent worse outcome. The least square mean change from baseline is being reported and negative values indicate an improvement in outcome.	Baseline up to Week 12
Primary	Least Square Mean Change From Baseline in the PANSS Positive Subscale (PANSS-P) Score	The PANSS 'P' Scale was calculated as the sum of the items prefixed with an P, 7 items in total, i.e. delusions, conceptual disorganization, hallucinatory behavior, excitement, grandiosity, suspiciousness/persecution and hostility. Individual items are rated on a 7-point scale, where 1 = absent and 7 = extreme. The least square mean change from baseline is being reported and negative values indicate an improvement in outcome.	Baseline up to Week 12
Primary	Least Square Mean Change From Baseline in the PANSS Negative Subscale (PANSS-N) Score	The PANSS 'N' Scale will be calculated as the sum of the items prefixed with an N, 7 items in total, i.e. blunted affect, emotional withdrawal, poor rapport, passive/apathetic social withdrawal, difficulty in abstract thinking, lack of spontaneity and flow of conversation and stereotyped thinking. Individual items are rated on a 7-point scale, where 1 = absent and 7 = extreme. The least square mean change from baseline is being reported and negative values indicate an improvement in outcome.	Baseline up to Week 12
Primary	Least Square Mean Change From Baseline in the PANSS General Subscale (PANSS-G) Score	The PANSS 'G' Scale will be calculated as the sum of the items prefixed with a G, 16 items in total, i.e. somatic concerns, anxiety, guilt feelings, tension, mannerisms and posturing, depression, motor retardation, uncooperativeness, unusual thought content, disorientation, poor attention, lack of judgment and insight, disturbance of volition, poor impulse control, preoccupation and active social avoidance. Individual items are rated on a 7-point scale, where 1 = absent and 7 = extreme. The least square mean change from baseline is being reported and negative values indicate an improvement in outcome.	Baseline up to Week 12
Primary	Least Square Mean Change From Baseline in the Clinical Global Impression of Severity (CGI-S) Score	The CGI-S is a 7-point scale used to rate the severity of participants' illness at the time of assessment. Considering total clinical experience, a participant will be assessed on severity of mental illness at the time of rating 0 = not assessed; 1 = normal, not at all ill; 2 = borderline mentally ill; 3 = mildly ill; 4 = moderately ill; 5 = markedly ill; 6 = severely ill; or 7 = among the most extremely ill participants. The least square mean change from baseline is being reported and negative values indicate an improvement in outcome.	Baseline up to Week 12
Primary	Number of Participants With Minimally or Better Clinical Global Impression of Improvement (CGI-I) Score at Week 12	The CGI-I is a 7-point scale used to rate the improvement of participants' condition at the time of assessment. Compared to the patient's condition at baseline, the participants' condition was rated as 1 = very much improved since initiation of treatment; 2 = much improved; 3 = minimally improved; 4 = no change from baseline; 5 = minimally worse; 6 = much worse; 7 = very much worse since the initiation of treatment. Higher scores indicate a worse outcome. The number of participants with minimally or better improvements (score of 3 or better) are being reported.	Week 12
Secondary	Mean Change From Baseline in Body Weight		Baseline up to Week 12
Secondary	Mean Change From Baseline in Body Mass Index (BMI)		Baseline up to Week 12
Secondary	Mean Change From Baseline in Waist Circumference		Baseline up to Week 12
Secondary	Mean Change From Baseline in Blood Pressure		Baseline up to Week 12
Secondary	Mean Change From Baseline in Heart Rate		Baseline up to Week 12
Secondary	Mean Change From Baseline in Respiratory Rate		Baseline up to Week 12
Secondary	Mean Change From Baseline in Temperature		Baseline up to Week 12
Secondary	Number of Participants With Clinically Significant Changes From Baseline in Clinical Laboratory Test Results		Day 85
Secondary	Number of Participants With Defined Flagged Electrocardiogram (ECG) Parameter Values		Day 85
Secondary	Number of Participants With Suicidal Ideation or Behavior Based on The Columbia Suicide Severity Rating Scale (C-SSRS)	The C-SSRS is a short questionnaire that is used to assess suicidal ideation (5 questions) and behavior (5 questions) since last patient visit. The questionnaire is completed by participants answering yes or no to each question.	Baseline (screening) up to Day 85