Combination Therapy of Deferiprone and N-Acetylcysteine for Treating Negative Symptoms in Schizophrenia (IronMan)
研究概览
详细说明
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:Amit Lotan
- 电话号码:+972-2-6777184
- 邮箱:amitlo@hadassah.org.il
学习地点
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Jerusalem、以色列
- Hadassah Medical Organization
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接触:
- Shlomo Rachmani
- 电话号码:+972-2-6777184
- 邮箱:shlomo80@hadassah.org.il
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Jerusalem、以色列
- Jerusalem Mental Health Center
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接触:
- Yoav Kohn
- 电话号码:1803 +972-2-6551303
- 邮箱:yoavk@ekmd.huji.ac.il
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参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion criteria:
- Aged 18-55 years.
- Diagnosis of schizophrenia/schizoaffective disorder according to the Diagnostic and Statistical Manual of Mental Disorders- Fifth Edition (DSM-5) criteria. The diagnostic assessment will be conducted using the Structured Clinical Interview for DSM-5 Clinical Trials Version (SCID-5-CT).
- Adequate antipsychotic treatment for ≥ 4 months prior to screening (excluding clozapine use).
- Stable dose of antipsychotic medication for ≥ 8 weeks prior to screening (excluding clozapine use).
- When relevant, stable dose of antidepressants, mood stabilizers and benzodiazepines/Z-drugs for ≥ 8 weeks prior to screening.
- Screening and baseline PANSS total score ranging from 60 to 120.
- Sum ≥ 20 for the 7 items in the Negative Symptoms subscale of the PANSS.
- At least two items in the PANSS Negative Symptoms subscale scored ≥ 4.
- Sum < 20 for the 7 items in the Positive Symptoms subscale of the PANSS.
- Score ≤ 5 for each item in the Positive Symptoms subscale of the PANSS.
- Calgary Depression Schizophrenia Scale (CDSS) score of ≤ 6.
- Persistent and predominant negative symptoms for ≥ 6 months, in the opinion of the investigator
- The subject exhibits clinical stability in both positive and negative symptoms of schizophrenia over the past 6 months, as assessed by the treating psychiatrist and supported by documentation in the medical record.
- No incarceration in prison or acute crisis intervention due to symptom exacerbation within 6 months of screening. The subject must be considered psychiatrically stable in the opinion of the investigator.
For males or postmenopausal women, either of the following:
- Serum ferritin ≥30 ng/mL at screening. OR
- Serum ferritin 15-29 ng/mL at screening, provided that:
i. An evaluation of potential underlying causes as well as potentially comorbid deficiencies has been completed, including assessment of folate, vitamin B12, celiac antibodies and H. pylori infection, and, in patients over 40 years old or with positive family history of colorectal cancer, also an appropriate colorectal screening test, alongside other tests deemed as relevant by the investigator; ii. Identified clinically significant causes have been appropriately managed; iii. Repeated ferritin assessment prior to randomization remains within the range of 15-29 ng/mL; and iv. Oral iron supplementation is initiated according to the study protocol.
- For premenopausal women: Serum ferritin ≥15 ng/mL at screening.
- Screening serum hemoglobin ≥ 13g/dL for males, ≥ 12g/dL for females
- Use of contraceptives in women of childbearing age.
- Ability to provide informed consent, confirmed by a non-study psychiatrist. When a subject is under guardianship, both patient assent and guardian consent are required. Obtaining written informed consent, dated and signed, is mandatory prior to the initiation of any procedures related to the clinical trial.
- Ability to safely undergo MRI scanning, assessed by a non-study psychiatrist.
- In the Investigator's opinion, the subject can understand the nature of the trial, comply with study drug administration and protocol procedures or has a guardian able to assist.
- Availability of a reliable caregiver or other responsible person (e.g., family member, social worker, nurse) to support treatment adherence and provide collateral information for rating scales.
Exclusion criteria:
- Primary DSM-5 diagnosis other than schizophrenia or schizoaffective disorder in the 12 months prior to screening, according to SCID-5-CT.
- Subjects diagnosed with Autistic Spectrum Disorder (ASD).
- Subjects diagnosed with Intellectual Developmental Disorder.
- Patients who received clozapine within the 6 months preceding the screening.
- Patients with a history of relapsing neutropenia (Absolute Neutrophile Count (ANC) < 1,500 cells/µL)
- Screening ANC ≤ 2,000 cells/µL.
- Non-compliance during run-in period (percent adherence ≤ 80%, as examined by pill count).
- Improvement > 20% in PANSS total score or PANSS negative subscale during the run-in period.
- Suicide attempt or serious suicidal behavior within the past 12 months.
- Risk for suicidal behavior during the study as determined by the investigator's clinical assessment and Columbia-Suicide Severity Rating Scale (C-SSRS).
- The subject has a history of substance use disorder or any illicit drug use (other than nicotine) within the past 3 years.
- Positive urine drug screen for drugs of abuse (cocaine, methadone, amphetamines, cannabinoids, opiates, and barbiturates).
- Risk of violent behavior in the opinion of the Investigator.
- Known hypersensitivity to deferiprone or N-Acetylcysteine.
- Pregnancy or intention to become pregnant during the study duration.
- Female patients who are lactating.
- ECT treatment within 18 weeks prior to screening and study entry.
- Patient with substantially confounding extrapyramidal symptoms (according to screening SAS, BARS, AIMS score).
- Conditions that are not suitable for partaking in an MRI scan, including metal implants and incompatible devices.
- Subjects with BMI ≤ 18 or ≥ 40.
- Participation in another clinical trial involving investigational drugs within 3 months prior to screening.
- Clinically significant general medical conditions (neurological, cardiovascular, respiratory, gastrointestinal, renal, hepatic, hematologic, oncologic) that could interfere with participation.
- Major active contagious disease.
- Patients with clinically significant abnormalities in hematology, blood chemistry, ECG or physical examination, not resolved by the Baseline visit, that can interfere with study participation.
- Any condition that, in the investigator's judgment, may compromise subject safety or interfere with study assessments.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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安慰剂比较:Placebo + N-Acetylcysteine
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This drug is given to both groups.
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有源比较器:Deferiprone + N-Acetylcysteine
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This drug is given to both groups.
This intervention has not been used before on Schizophrenia or Schizoaffective patients with predominant negative symptoms.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Change in Total PANSS Score
大体时间:36 Weeks (LOCF)
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Change from Baseline to Week 36 in the PANSS (Positive and Negative Syndrome Scale) total score.
PANSS total score range: 30 to 210 (30 items, each rated 1-7, so minimum 30 and maximum 210).
Higher scores indicate more severe symptoms.
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36 Weeks (LOCF)
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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PANSS Marder Negative Symptom Factor Score
大体时间:12, 24 and 36 weeks
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Change from Baseline in the PANSS Marder Negative Symptom Factor Score (NSF)
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12, 24 and 36 weeks
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PANSS Positive Subscale Score
大体时间:12, 24 and 36 weeks
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Change from Baseline in the PANSS Positive sub-scale score
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12, 24 and 36 weeks
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PANSS Negative Subscale Score
大体时间:12, 24 and 36 weeks
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Change from Baseline in the PANSS Negative sub-scale score
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12, 24 and 36 weeks
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PANSS General Psychopathological Subscale Score
大体时间:12, 24 and 36 weeks
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Change from Baseline in the PANSS General Psychopathological sub-scale score
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12, 24 and 36 weeks
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BNSS (Brief Negative Symptom Scale) Score
大体时间:12, 24 and 36 weeks
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Change from Baseline in the BNSS (Brief Negative Symptom Scale) score
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12, 24 and 36 weeks
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BACS (Brief Cognitive Assessment in Schizophrenia) Score
大体时间:12, 24 and 36 weeks
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Change from Baseline in the BACS (Brief Cognitive Assessment in Schizophrenia) score
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12, 24 and 36 weeks
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Reported adverse events (descriptive)
大体时间:From enrollment to the end of treatment at 36 weeks
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Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Weight (kg)
大体时间:From enrollment to the end of treatment at 36 weeks
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Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Height (cm)
大体时间:From enrollment to the end of treatment at 36 weeks
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Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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BMI (Body Mass Index, kg/cm^2)
大体时间:From enrollment to the end of treatment at 36 weeks
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Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Blood pressure (mm Hg)
大体时间:From enrollment to the end of treatment at 36 weeks
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Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Heart rate (BPM)
大体时间:From enrollment to the end of treatment at 36 weeks
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Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Electrocardiogram (ECG)
大体时间:From enrollment to the end of treatment at 36 weeks
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Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Complete Blood Count (CBC)
大体时间:From enrollment to the end of treatment at 36 weeks
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Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Serum creatinine
大体时间:From enrollment to the end of treatment at 36 weeks
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kidney function test, mg/dL, Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Serum alanine transaminase
大体时间:From enrollment to the end of treatment at 36 weeks
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ALT, liver function test, U/L, Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Serum ferritin
大体时间:From enrollment to the end of treatment at 36 weeks
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iron store index, ng/mL, Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Simpson-Angus Extrapyramidal Rating Scale (SAS)
大体时间:From enrollment to the end of treatment at 36 weeks
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10 items, each 0-4, Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Barnes Akathisia Rating Scale (BARS)
大体时间:From enrollment to the end of treatment at 36 weeks
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Global clinical assessment of akathisia (0-5), Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Abnormal Involuntary Movement Scale (AIMS)
大体时间:From enrollment to the end of treatment at 36 weeks
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Items counted: 7, Per-item range: 0-4, Total (sum) range: 0-28, Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Columbia-Suicide Severity Rating Scale (C-SSRS)
大体时间:From enrollment to the end of treatment at 36 weeks
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Ideation severity: 0-5, Ideation intensity (sum): 0-25, Behavior: categorical (yes/no; counts), Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Udvalg for Kliniske Undersøgelser Side Effect Rating Scale (UKU-SERS )
大体时间:From enrollment to the end of treatment at 36 weeks
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Per item range: 0-3 (0 = none, 1 = mild, 2 = moderate, 3 = marked/severe), Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Discontinuation-Emergent Signs and Symptoms (DESS)
大体时间:From enrollment to the end of treatment at 36 weeks
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43-item checklist: each symptom is scored 0/1 (absent/present), total range 0-43; Safety and tolerability assessment
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From enrollment to the end of treatment at 36 weeks
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Quantitative MRI - Proton Density (PD)
大体时间:baseline, 36 weeks
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PD is normalized to derive the water fraction (WF); WF yields the Macromolecular Tissue Volume (MTV).
These reflect the ratio of water to non water tissue and act as biomarkers of atrophy or density
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baseline, 36 weeks
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Quantitative MRI - R1 (Longitudinal Relaxation Rate)
大体时间:Baseline, 36 weeks
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R1 is sensitive to myelin, iron and water content.
R1 and MTV are acquired using the same variable flip angle or/and MP2RAGE sequences, which can also include MT and multi echo acquisitions for R2* and QSM
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Baseline, 36 weeks
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Quantitative MRI - Magnetization Transfer (MT)
大体时间:Baseline, 36 weeks
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MT modeling estimates the macromolecular contribution to R1, yielding MTsat.
Combined with R1 and MTV, this enables R1sat and MTVsat estimation, providing contrast related to saturated vs. unsaturated water pools
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Baseline, 36 weeks
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Quantitative MRI - R2*
大体时间:Baseline, 36 weeks
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R2* is influenced by magnetic field inhomogeneities and is sensitive to iron deposition and other sources
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Baseline, 36 weeks
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Quantitative MRI - Quantitative Susceptibility Mapping (QSM)
大体时间:Baseline, 36 weeks
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QSM estimates tissue magnetic susceptibility from R2* data and is sensitive to iron, calcium and related tissue properties
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Baseline, 36 weeks
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Quantitative MRI - R2 (Transverse Relaxation Rate)
大体时间:Baseline, 36 weeks
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R2 reflects tissue integrity and is influenced by myelin and iron.
Multi-component fitting allows estimation of Myelin Water Fraction (MWF)
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Baseline, 36 weeks
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Quantitative MRI - R1-R2 Relaxivity
大体时间:Baseline, 36 weeks
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The voxel-wise slope of R1 vs. R2* within an ROI (R1-R2* relaxivity) can reflect specific iron forms
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Baseline, 36 weeks
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Quantitative MRI - Tissue Relaxivity (MTV Dependency)
大体时间:Baseline, 36 weeks
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Parameter-MTV slope (MDM: Multidimensional Dependency on MTV) reflects lipid and macromolecular composition
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Baseline, 36 weeks
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Quantitative MRI - Diffusion MRI
大体时间:Baseline, 36 weeks
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Mean Diffusivity (MD)
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Baseline, 36 weeks
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Quantitative MRI - Diffusion MRI
大体时间:Baseline, 36 weeks
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Fractional Anisotropy (FA)
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Baseline, 36 weeks
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Quantitative MRI - G-Ratio Mapping
大体时间:Baseline, 36 weeks
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Combines diffusion (axon density) and qMRI (myelin) data to estimate the g-ratio: the ratio of axon to fiber diameter
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Baseline, 36 weeks
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Quantitative MRI - Macroscopic Morphometry
大体时间:Baseline, 36 weeks
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Cortical volume
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Baseline, 36 weeks
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Quantitative MRI - Neuromelanin-Sensitive MRI (NM-MRI)
大体时间:Baseline, 36 weeks
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T1-weighted or MT-enhanced sequences detect neuromelanin in the substantia nigra and locus coeruleus; used to assess catecholaminergic neuron integrity
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Baseline, 36 weeks
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Magnetic Resonance Spectroscopy (MRS)
大体时间:Baseline, 36 weeks
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Estimates concentrations of brain metabolites
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Baseline, 36 weeks
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Proportion of patients showing a PANSS response of ≥30% reduction
大体时间:12, 24 and 36 weeks
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Proportion of patients showing a PANSS response of ≥30% reduction in corrected PANSS total score (PANSS total minus 30)
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12, 24 and 36 weeks
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CDSS (Calgary Depression Scale for Schizophrenia) Scale
大体时间:12, 24 and 36 weeks
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Change from Baseline in CDSS (Calgary Depression Scale for Schizophrenia) scale
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12, 24 and 36 weeks
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CGI-Schizophrenia (CGI-SCH) : Negative Symptoms Severity of Illness sub-scale
大体时间:12, 24 and 36 weeks
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Change from Baseline in the CGI-Schizophrenia (CGI-SCH) Scale : Negative Symptoms - Severity of Illness sub-scale; Scale: 1-7; 1 = Normal, not ill; 7 = Among the most extremely ill patients
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12, 24 and 36 weeks
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CGI-Schizophrenia (CGI-SCH) : Overall Severity of Illness sub-scale
大体时间:12, 24 and 36 weeks
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Change from Baseline in the CGI-Schizophrenia (CGI-SCH) Scale : Overall Severity of Illness sub-scale; Scale: 1-7; 1 = Normal, not ill; 7 = Among the most extremely ill patients
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12, 24 and 36 weeks
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CGI-Schizophrenia (CGI-SCH) : Overall Degree of Change sub-scale
大体时间:12, 24 and 36 weeks
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Change from Baseline in the CGI-Schizophrenia (CGI-SCH) Scale : Overall Degree of Change sub-scale; Scale: 1-7, 1 = Very much improved, 4 = No change, 7 = Very much worse
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12, 24 and 36 weeks
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Personal and Social Performance (PSP) Scale
大体时间:12, 24 and 36 weeks
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Change from Baseline in Personal and Social Performance (PSP) scale
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12, 24 and 36 weeks
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Self-evaluation of Negative Symptoms (SNS) Scale
大体时间:12, 24 and 36 weeks
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Change from Baseline in the Self-evaluation of Negative Symptoms (SNS) scale
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12, 24 and 36 weeks
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合作者和调查者
出版物和有用的链接
一般刊物
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