Actively Recruiting
The Effect of a Six Week Intensified Pharmacological Treatment for Schizophrenia Compared to Treatment as Usual in Subjects Who Had a First-time Treatment Failure on Their First-line Treatment.
Led by Dr. Inge Winter · Updated on 2025-09-26
418
Participants Needed
13
Research Sites
204 weeks
Total Duration
On this page
Sponsors
D
Dr. Inge Winter
Lead Sponsor
U
Universität Münster
Collaborating Sponsor
AI-Summary
What this Trial Is About
Schizophrenia (SZ) affects approximately 4.5 million people across the European Union (EU) and is associated with annual healthcare and societal costs of 29 billion Euros. The impact on the daily life of patients is huge, ranging from frequent relapses and hospitalisations, the inability to maintain a job or continue scholing, to a low quality of life, impaired cognitive functioning, suicidal ideation and an increase morbidity rate, next to the large burden for carers 1. When diagnosed with schizophrenia or related disorder, patients are commonly prescribed antipsychotics. One-third of the schizophrenia patients are regarded treatment-resistant (TR), meaning that at least two antipsychotic trials have failed. Typically, clozapine is prescribed for TR patients, which is effective for approximately 40% of patients. Clozapine is among the most effective treatments, with the lowest all-cause mortality. Although it is among the most effective antipsychotics, it is generally not used earlier in the illness course due to a small risk of severe neutropenia/agranulocytosis, which is why patients treated with clozapine are intensely monitored. However, this small risk outweighs the burden of not receiving an effective treatment. Since clozapine is among the most effective treatments, this leads to the research question whether earlier initiation of third-line treatment ('early intensified' pharmacological treatment; EIPT) would be more beneficial than the current second-line treatments (treatment as usual; TAU). If this is indeed the case, this could lead to the prevention of unnecessary trials of ineffective treatments, hospitalisations, and recommendations for adaptations of worldwide guidelines as well as a reduction of healthcare and societal costs The INTENSIFY-Schizophrenia trial is part of the larger Horizon 2021 project Psych-STRATA, with the central goal of paving the way for a shift towards a treatment decision-making process tailored for the individual at risk for treatment resistance. To that end, the inestigators aim to establish evidence-based criteria to make decisions of early intense treatment in individuals at risk for treatment resistance across the major psychiatric disorders of schizophrenia, bipolar disorder and major depression. The current protocol focuses on the sample of schizophrenia patients.
CONDITIONS
Official Title
The Effect of a Six Week Intensified Pharmacological Treatment for Schizophrenia Compared to Treatment as Usual in Subjects Who Had a First-time Treatment Failure on Their First-line Treatment.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male and female patients aged 18 to 70 years
- Willing and able to provide written informed consent; legal guardian cosign allowed
- Female participants of childbearing potential must use effective contraception and have a negative pregnancy test before randomization
- Diagnosed with schizophrenia, schizoaffective disorder, or schizophreniform disorder confirmed by MINI interview
- Experiencing treatment failure due to lack of efficacy in the current episode, confirmed by Clinical Global Impression-Improvement score of 3 or higher
- Current treatment is preferably a first-line antipsychotic given for at least 4 weeks at an effective dose, but other treatments accepted
- Subject and clinician intend to change pharmacological treatment
- Minimum symptom severity: at least two PANSS positive or negative items scored 4 or higher, or one scored 5 or higher
- Functional impairment score of 5 or higher on any Sheehan Disability Scale section
You will not qualify if you...
- Pregnant or breastfeeding
- Prior use of clozapine
- Known intolerance to clozapine or all treatment as usual medications
- Contraindications to clozapine or all treatment as usual medications per product characteristics
- Participation in another clinical trial with investigational drug within 30 days before screening
- Significant disease or disorder that poses risk or affects trial results or participation
- Active suicidal ideation with intent or plan as assessed by clinician
- Current severe substance use disorder excluding nicotine, mild/moderate alcohol or cannabis use
- Institutionalized by judicial or administrative order
- Meets criteria for clinical remission by modified Andreasen criteria
- Clinically significant abnormal lab, ECG, or physical exam findings
- Dependency on sponsor, investigator, or trial site
AI-Screening
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Trial Site Locations
Total: 13 locations
1
Medical University Innsbruck
Innsbruck, Austria
Actively Recruiting
2
Bezirkskliniken Schwaben, Bezirkskrankenhaus Augsburg
Augsburg, Germany, 86156
Not Yet Recruiting
3
Universitätsklinik für Psychiatrie und Psychotherapie Bielefeld
Bielefeld, Germany
Actively Recruiting
4
LWL-Klinik Dortmund, Bereich Forschung & Wissenschaft
Dortmund, Germany, 44287
Actively Recruiting
5
University Hospital Frankfurt am Main - Goethe University
Frankfurt am Main, Germany
Actively Recruiting
6
Klinik für Psychiatrie und Psychotherapie der Universitätsmedizin Mainz
Mainz, Germany
Actively Recruiting
7
Westfälische Wilhelms-Universität Münster
Münster, Germany
Actively Recruiting
8
Universita degli Studi di Brescia
Brescia, Italy
Actively Recruiting
9
University of Cagliari
Cagliari, Italy
Actively Recruiting
10
Università degli studi della Campania Luigi Vanvitelli
Naples, Italy, 80138
Actively Recruiting
11
Azienda Ospedaliero-Universitaria "Città della Salute e della Scienza di Torino"
Turin, Italy
Actively Recruiting
12
Fundació Clínic per a la Recerca Biomèdica
Barcelona, Spain
Actively Recruiting
13
King's College London, Psychiatry & Cognitive Neuroscience
London, United Kingdom, SE5 8AF
Actively Recruiting
Research Team
I
Inge Winter, Dr.
CONTACT
C
Cynthia Okhuijsen-Pfeifer, Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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