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Combination Therapy of Deferiprone and N-Acetylcysteine for Treating Negative Symptoms in Schizophrenia (IronMan)

9 août 2026 mis à jour par: Amit Lotan
In following guidelines for studying negative symptoms in schizophrenia, 60 patients aged 18-40, diagnosed with schizophrenia or schizoaffective disorder during the last ten years, will receive a combination of the iron chelator DFP plus NAC or a matching placebo plus NAC combination, as add-on to their maintenance antipsychotic drug (APD) treatment, for a duration of 36 weeks. Prior to initiation of treatment, all participants will undergo baseline MRI scan. A follow-up MRI will be conducted at the end of the 36-week study period, or upon early withdrawal if applicable, to evaluate the effect of the add-on treatment on iron dyshomeostasis and morphology.

Aperçu de l'étude

Description détaillée

The present study is designed as an interventional trial over a 36-week period per patient. The target populThe present study is designed as an interventional trial over a 36-week period per patient. The target population consists of patients with schizophrenia (age 18-40 years), up to ten years since onset of positive symptoms. The overall objective of the study is to assess the safety and efficacy of DFP-NAC combination add-on in patients with schizophrenia, compared to NAC-only add-on (control group). This study is designed to test the hypothesis that, in patients with prominent negative symptoms, adjunctive treatment with DFP-NAC combination will demonstrate a favorable safety profile and produce clinical improvements in negative and cognitive domains of schizophrenia beyond those offered by addition of NAC alone.ation consists of patients with schizophrenia (age 18-40 years), up to ten years since onset of positive symptoms. The overall objective of the study is to assess the safety and efficacy of DFP-NAC combination add-on in patients with schizophrenia, compared to NAC-only add-on (control group). This study is designed to test the hypothesis that, in patients with prominent negative symptoms, adjunctive treatment with DFP-NAC combination will demonstrate a favorable safety profile and produce clinical improvements in negative and cognitive domains of schizophrenia beyond those offered by addition of NAC alone.

Type d'étude

Interventionnel

Inscription (Estimé)

80

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

      • Jerusalem, Israël
        • Hadassah Medical Organization
        • Contact:
      • Jerusalem, Israël
        • Jerusalem Mental Health Center
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Oui

La description

Inclusion criteria:

  1. Aged 18-55 years.
  2. 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).
  3. Adequate antipsychotic treatment for ≥ 4 months prior to screening (excluding clozapine use).
  4. Stable dose of antipsychotic medication for ≥ 8 weeks prior to screening (excluding clozapine use).
  5. When relevant, stable dose of antidepressants, mood stabilizers and benzodiazepines/Z-drugs for ≥ 8 weeks prior to screening.
  6. Screening and baseline PANSS total score ranging from 60 to 120.
  7. Sum ≥ 20 for the 7 items in the Negative Symptoms subscale of the PANSS.
  8. At least two items in the PANSS Negative Symptoms subscale scored ≥ 4.
  9. Sum < 20 for the 7 items in the Positive Symptoms subscale of the PANSS.
  10. Score ≤ 5 for each item in the Positive Symptoms subscale of the PANSS.
  11. Calgary Depression Schizophrenia Scale (CDSS) score of ≤ 6.
  12. Persistent and predominant negative symptoms for ≥ 6 months, in the opinion of the investigator
  13. 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.
  14. 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.
  15. For males or postmenopausal women, either of the following:

    1. Serum ferritin ≥30 ng/mL at screening. OR
    2. 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.

  16. For premenopausal women: Serum ferritin ≥15 ng/mL at screening.
  17. Screening serum hemoglobin ≥ 13g/dL for males, ≥ 12g/dL for females
  18. Use of contraceptives in women of childbearing age.
  19. 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.
  20. Ability to safely undergo MRI scanning, assessed by a non-study psychiatrist.
  21. 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.
  22. 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:

  1. Primary DSM-5 diagnosis other than schizophrenia or schizoaffective disorder in the 12 months prior to screening, according to SCID-5-CT.
  2. Subjects diagnosed with Autistic Spectrum Disorder (ASD).
  3. Subjects diagnosed with Intellectual Developmental Disorder.
  4. Patients who received clozapine within the 6 months preceding the screening.
  5. Patients with a history of relapsing neutropenia (Absolute Neutrophile Count (ANC) < 1,500 cells/µL)
  6. Screening ANC ≤ 2,000 cells/µL.
  7. Non-compliance during run-in period (percent adherence ≤ 80%, as examined by pill count).
  8. Improvement > 20% in PANSS total score or PANSS negative subscale during the run-in period.
  9. Suicide attempt or serious suicidal behavior within the past 12 months.
  10. Risk for suicidal behavior during the study as determined by the investigator's clinical assessment and Columbia-Suicide Severity Rating Scale (C-SSRS).
  11. The subject has a history of substance use disorder or any illicit drug use (other than nicotine) within the past 3 years.
  12. Positive urine drug screen for drugs of abuse (cocaine, methadone, amphetamines, cannabinoids, opiates, and barbiturates).
  13. Risk of violent behavior in the opinion of the Investigator.
  14. Known hypersensitivity to deferiprone or N-Acetylcysteine.
  15. Pregnancy or intention to become pregnant during the study duration.
  16. Female patients who are lactating.
  17. ECT treatment within 18 weeks prior to screening and study entry.
  18. Patient with substantially confounding extrapyramidal symptoms (according to screening SAS, BARS, AIMS score).
  19. Conditions that are not suitable for partaking in an MRI scan, including metal implants and incompatible devices.
  20. Subjects with BMI ≤ 18 or ≥ 40.
  21. Participation in another clinical trial involving investigational drugs within 3 months prior to screening.
  22. Clinically significant general medical conditions (neurological, cardiovascular, respiratory, gastrointestinal, renal, hepatic, hematologic, oncologic) that could interfere with participation.
  23. Major active contagious disease.
  24. 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.
  25. Any condition that, in the investigator's judgment, may compromise subject safety or interfere with study assessments.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur placebo: Placebo + N-Acetylcysteine
This drug is given to both groups.
Comparateur actif: Deferiprone + N-Acetylcysteine
This drug is given to both groups.
This intervention has not been used before on Schizophrenia or Schizoaffective patients with predominant negative symptoms.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in Total PANSS Score
Délai: 36 Weeks (LOCF)
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.
36 Weeks (LOCF)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
PANSS Marder Negative Symptom Factor Score
Délai: 12, 24 and 36 weeks
Change from Baseline in the PANSS Marder Negative Symptom Factor Score (NSF)
12, 24 and 36 weeks
PANSS Positive Subscale Score
Délai: 12, 24 and 36 weeks
Change from Baseline in the PANSS Positive sub-scale score
12, 24 and 36 weeks
PANSS Negative Subscale Score
Délai: 12, 24 and 36 weeks
Change from Baseline in the PANSS Negative sub-scale score
12, 24 and 36 weeks
PANSS General Psychopathological Subscale Score
Délai: 12, 24 and 36 weeks
Change from Baseline in the PANSS General Psychopathological sub-scale score
12, 24 and 36 weeks
BNSS (Brief Negative Symptom Scale) Score
Délai: 12, 24 and 36 weeks
Change from Baseline in the BNSS (Brief Negative Symptom Scale) score
12, 24 and 36 weeks
BACS (Brief Cognitive Assessment in Schizophrenia) Score
Délai: 12, 24 and 36 weeks
Change from Baseline in the BACS (Brief Cognitive Assessment in Schizophrenia) score
12, 24 and 36 weeks
Reported adverse events (descriptive)
Délai: From enrollment to the end of treatment at 36 weeks
Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Weight (kg)
Délai: From enrollment to the end of treatment at 36 weeks
Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Height (cm)
Délai: From enrollment to the end of treatment at 36 weeks
Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
BMI (Body Mass Index, kg/cm^2)
Délai: From enrollment to the end of treatment at 36 weeks
Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Blood pressure (mm Hg)
Délai: From enrollment to the end of treatment at 36 weeks
Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Heart rate (BPM)
Délai: From enrollment to the end of treatment at 36 weeks
Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Electrocardiogram (ECG)
Délai: From enrollment to the end of treatment at 36 weeks
Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Complete Blood Count (CBC)
Délai: From enrollment to the end of treatment at 36 weeks
Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Serum creatinine
Délai: From enrollment to the end of treatment at 36 weeks
kidney function test, mg/dL, Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Serum alanine transaminase
Délai: From enrollment to the end of treatment at 36 weeks
ALT, liver function test, U/L, Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Serum ferritin
Délai: From enrollment to the end of treatment at 36 weeks
iron store index, ng/mL, Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Simpson-Angus Extrapyramidal Rating Scale (SAS)
Délai: From enrollment to the end of treatment at 36 weeks
10 items, each 0-4, Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Barnes Akathisia Rating Scale (BARS)
Délai: From enrollment to the end of treatment at 36 weeks
Global clinical assessment of akathisia (0-5), Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Abnormal Involuntary Movement Scale (AIMS)
Délai: From enrollment to the end of treatment at 36 weeks
Items counted: 7, Per-item range: 0-4, Total (sum) range: 0-28, Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Columbia-Suicide Severity Rating Scale (C-SSRS)
Délai: From enrollment to the end of treatment at 36 weeks
Ideation severity: 0-5, Ideation intensity (sum): 0-25, Behavior: categorical (yes/no; counts), Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Udvalg for Kliniske Undersøgelser Side Effect Rating Scale (UKU-SERS )
Délai: From enrollment to the end of treatment at 36 weeks
Per item range: 0-3 (0 = none, 1 = mild, 2 = moderate, 3 = marked/severe), Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Discontinuation-Emergent Signs and Symptoms (DESS)
Délai: From enrollment to the end of treatment at 36 weeks
43-item checklist: each symptom is scored 0/1 (absent/present), total range 0-43; Safety and tolerability assessment
From enrollment to the end of treatment at 36 weeks
Quantitative MRI - Proton Density (PD)
Délai: baseline, 36 weeks
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
baseline, 36 weeks
Quantitative MRI - R1 (Longitudinal Relaxation Rate)
Délai: Baseline, 36 weeks
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
Baseline, 36 weeks
Quantitative MRI - Magnetization Transfer (MT)
Délai: Baseline, 36 weeks
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
Baseline, 36 weeks
Quantitative MRI - R2*
Délai: Baseline, 36 weeks
R2* is influenced by magnetic field inhomogeneities and is sensitive to iron deposition and other sources
Baseline, 36 weeks
Quantitative MRI - Quantitative Susceptibility Mapping (QSM)
Délai: Baseline, 36 weeks
QSM estimates tissue magnetic susceptibility from R2* data and is sensitive to iron, calcium and related tissue properties
Baseline, 36 weeks
Quantitative MRI - R2 (Transverse Relaxation Rate)
Délai: Baseline, 36 weeks
R2 reflects tissue integrity and is influenced by myelin and iron. Multi-component fitting allows estimation of Myelin Water Fraction (MWF)
Baseline, 36 weeks
Quantitative MRI - R1-R2 Relaxivity
Délai: Baseline, 36 weeks
The voxel-wise slope of R1 vs. R2* within an ROI (R1-R2* relaxivity) can reflect specific iron forms
Baseline, 36 weeks
Quantitative MRI - Tissue Relaxivity (MTV Dependency)
Délai: Baseline, 36 weeks
Parameter-MTV slope (MDM: Multidimensional Dependency on MTV) reflects lipid and macromolecular composition
Baseline, 36 weeks
Quantitative MRI - Diffusion MRI
Délai: Baseline, 36 weeks
Mean Diffusivity (MD)
Baseline, 36 weeks
Quantitative MRI - Diffusion MRI
Délai: Baseline, 36 weeks
Fractional Anisotropy (FA)
Baseline, 36 weeks
Quantitative MRI - G-Ratio Mapping
Délai: Baseline, 36 weeks
Combines diffusion (axon density) and qMRI (myelin) data to estimate the g-ratio: the ratio of axon to fiber diameter
Baseline, 36 weeks
Quantitative MRI - Macroscopic Morphometry
Délai: Baseline, 36 weeks
Cortical volume
Baseline, 36 weeks
Quantitative MRI - Neuromelanin-Sensitive MRI (NM-MRI)
Délai: Baseline, 36 weeks
T1-weighted or MT-enhanced sequences detect neuromelanin in the substantia nigra and locus coeruleus; used to assess catecholaminergic neuron integrity
Baseline, 36 weeks
Magnetic Resonance Spectroscopy (MRS)
Délai: Baseline, 36 weeks
Estimates concentrations of brain metabolites
Baseline, 36 weeks

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Proportion of patients showing a PANSS response of ≥30% reduction
Délai: 12, 24 and 36 weeks
Proportion of patients showing a PANSS response of ≥30% reduction in corrected PANSS total score (PANSS total minus 30)
12, 24 and 36 weeks
CDSS (Calgary Depression Scale for Schizophrenia) Scale
Délai: 12, 24 and 36 weeks
Change from Baseline in CDSS (Calgary Depression Scale for Schizophrenia) scale
12, 24 and 36 weeks
CGI-Schizophrenia (CGI-SCH) : Negative Symptoms Severity of Illness sub-scale
Délai: 12, 24 and 36 weeks
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
12, 24 and 36 weeks
CGI-Schizophrenia (CGI-SCH) : Overall Severity of Illness sub-scale
Délai: 12, 24 and 36 weeks
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
12, 24 and 36 weeks
CGI-Schizophrenia (CGI-SCH) : Overall Degree of Change sub-scale
Délai: 12, 24 and 36 weeks
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
12, 24 and 36 weeks
Personal and Social Performance (PSP) Scale
Délai: 12, 24 and 36 weeks
Change from Baseline in Personal and Social Performance (PSP) scale
12, 24 and 36 weeks
Self-evaluation of Negative Symptoms (SNS) Scale
Délai: 12, 24 and 36 weeks
Change from Baseline in the Self-evaluation of Negative Symptoms (SNS) scale
12, 24 and 36 weeks

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 septembre 2026

Achèvement primaire (Estimé)

1 décembre 2028

Achèvement de l'étude (Estimé)

1 décembre 2029

Dates d'inscription aux études

Première soumission

20 novembre 2025

Première soumission répondant aux critères de contrôle qualité

9 août 2026

Première publication (Réel)

12 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

12 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

9 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

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INDÉCIS

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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