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Recruiting Phase 1, Phase 2 NCT03971487

NCT03971487 Ocrelizumab for Psychosis by Autoimmunity

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Clinical Trial Summary
NCT ID NCT03971487
Status Recruiting
Phase Phase 1, Phase 2
Sponsor The Methodist Hospital Research Institute
Condition Schizo-Affective Type of Psychosis
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2019-10-01
Primary Completion 2028-06-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 35 Years
Study Type INTERVENTIONAL
Interventions
Psychosis and cognitive assessmentsPhysical and neuro-cognitive evaluationsSafety labs and electrocardiogram

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

Phase 1 is the earliest stage of human testing — safety and dosage are the primary focus. Visits are frequent and medical supervision is intensive. You will be among the first people to receive this treatment.

This trial targets 40 participants in total. It began in 2019-10-01 with a primary completion date of 2028-06-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Some people who have what doctors currently call schizophrenia or bipolar disease may actually have a brain disease caused by auto-antibodies. Auto-antibodies are produced when the normal defense mechanism of the body goes wrong and begins to attack the body, similar to "friendly fire." Auto-antibodies attack brain receptors and then the person who has this problem begins to have hallucinations and other manifestations of schizophrenia, like feeling that people can see what they are thinking and also feeling that other people do not like them. If this disease is caused by auto-antibodies, typically the person is well until they are 15 years of age or older, but seldom older than 35 years. Then, in a matter of a few months they begin to have hallucinations and the other symptoms. Doctors still do not know whether some people with schizophrenia or bipolar disease have auto-antibodies attacking their brain. For this reason, in this study some of these patients will receive a treatment that suppresses the auto-antibodies and their symptoms after treatment will be compared with the symptoms of a group of similar patients who are given a preparation that looks like the real treatment, but it is not.

Eligibility Criteria

Inclusion Criteria: * Individuals of either sex, 18-35 years of age. * Having an active psychotic disorder meeting DSM-5 criteria, including a duration of at least six months, for Schizophrenia Spectrum Disorder, as defined by the Mini International Neuropsychiatric Interview (MINI). * A total PANSS ≥ 60 and a score ≥ 4 on at least 2 of the PANSS positive symptoms. * Normal academic performance at least until the age of 15 years and absence of psychiatric symptoms before the same age. * Ability to assent or consent to the performance of the study and participate in testing procedures. Exclusion Criteria: * The dose of antipsychotic medication (if they are on one) has been changed less than two weeks prior to baseline PANSS testing (Visit 2, see below). * Patient treated with a medication designed to suppress the immune system, other than standard analgesics or antipyretics, in the six months prior to randomization. * Vaccinated with a live-attenuated vaccine less than 4 weeks before ocrelizumab infusion or with a non-live vaccine less than 2 weeks before infusion. * Active infection, or history of or known presence of recurrent or chronic infection (for example, hepatitis B or C, Human Immunodeficiency Virus, syphilis, tuberculosis, PML). * History of brain tumor, stroke, severe head trauma or multiple sclerosis. * Active cancer, metabolic encephalopathy, severe cardiovascular or renal disease. * In the judgment of the PI, psychosis related to substance abuse or metabolic disorders. * Pregnancy or lactation. * Requirement for chronic treatment with systemic corticosteroids or immunosuppressants during the course of the study. * History of or currently active primary or secondary immunodeficiency. * History of severe allergic or anaphylactic reactions to humanized or murine monoclonal antibodies. * Contraindications to or intolerance of oral or IV corticosteroids.

Contact & Investigator

Central Contact

Joseph C Masdeu, MD, PhD

✉ jcmasdeu@houstonmethodist.org

📞 202-255-7899

Principal Investigator

Joseph C Masdeu, MD, PhD

PRINCIPAL INVESTIGATOR

HOUSTON METHODIST NEUROLOGICAL INSTITUTE

Frequently Asked Questions

Who can join the NCT03971487 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 35 Years, studying Schizo-Affective Type of Psychosis. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT03971487 trial and what does that mean for participants?

Phase 1 trials are the first stage of human testing. The primary goal is to assess safety and determine appropriate dosage levels. Participants are closely monitored. These trials typically involve a small number of volunteers.

Is NCT03971487 currently recruiting?

Yes, NCT03971487 is actively recruiting participants. Contact the research team at jcmasdeu@houstonmethodist.org for enrollment information.

Where is the NCT03971487 trial being conducted?

This trial is being conducted at Houston, United States.

Who is sponsoring the NCT03971487 clinical trial?

NCT03971487 is sponsored by The Methodist Hospital Research Institute. The principal investigator is Joseph C Masdeu, MD, PhD at HOUSTON METHODIST NEUROLOGICAL INSTITUTE. The trial plans to enroll 40 participants.

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