← Back to Search

Other

Roluperidone + Olanzapine for Schizophrenia

Phase 1
Waitlist Available
Research Sponsored by Minerva Neurosciences
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up screening, baseline, days 1, 7, 8, and 17, and day 31
Awards & highlights
No Placebo-Only Group

Summary

This trial is testing the safety and effectiveness of using two medications, Roluperidone and Olanzapine, together in adults with severe schizophrenia symptoms. The goal is to see if this combination can better improve mood and behavior by affecting brain chemicals.

Who is the study for?
Adults with schizophrenia for at least a year, BMI under 35, stable symptoms, and not on conflicting meds can join. They must have moderate to severe negative symptoms but no major depressive or bipolar disorder. Women of childbearing potential need double contraception.
What is being tested?
The trial tests Roluperidone alone for a week then combined with Olanzapine for another ten days in adults with schizophrenia. It aims to understand the safety and how these drugs work together when taken by patients.
What are the potential side effects?
Potential side effects may include typical antipsychotic reactions like drowsiness, weight gain, dry mouth, restlessness (akathisia), increased blood sugar or cholesterol levels. Specific side effects from combining these drugs are being studied.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~screening, baseline, days 1, 7, 8, and 17, and day 31
This trial's timeline: 3 weeks for screening, Varies for treatment, and screening, baseline, days 1, 7, 8, and 17, and day 31 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Abnormal Involuntary Movement Scale (AIMS)
Adverse events
Barnes Akathisia Rating Scale (BARS)
+10 more
Other study objectives
Calgary Depression Scale for Schizophrenia (CDSS)
Clinical Global Impression - Severity Rating (CGI-S)
Positive and Negative Symptoms Scale (PANSS)

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: Treatment Phase 2Experimental Treatment2 Interventions
Roluperidone 64 mg oral and olanzapine 10 mg oral administered at the same time daily for 10 days on Days 8-17.
Group II: Treatment Phase 1Experimental Treatment1 Intervention
Roluperidone 64 mg monotherapy administered as an oral dose daily for 7 days on Days 1-7.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Roluperidone 64 mg
2017
Completed Phase 3
~540
Olanzapine 10 MG
2023
Completed Phase 1
~20

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for schizophrenia, such as Roluperidone and Olanzapine, work by antagonizing dopamine D2 and serotonin 5-HT2A receptors. This dual action helps reduce positive symptoms like hallucinations and delusions by modulating dopamine activity, while also addressing negative symptoms and cognitive deficits through serotonin receptor antagonism. Understanding these mechanisms is important for patients as it explains how these medications can improve their symptoms and informs them about potential side effects, aiding in better management of their condition.
Brexpiprazole and cariprazine: distinguishing two new atypical antipsychotics from the original dopamine stabilizer aripiprazole.Treatment of early onset schizophrenia: recent trends, challenges and future considerations.Schizophrenia - advances in drug therapy.

Find a Location

Who is running the clinical trial?

Minerva NeurosciencesLead Sponsor
5 Previous Clinical Trials
944 Total Patients Enrolled
~8 spots leftby Nov 2025