Research Study for Adults with First Episode/Early Phase Schizophrenia

Research Study for Adults with First Episode/Early Phase Schizophrenia

01 Oct 2025
Illinois, Chicago, 60601 Chicago USA

Research Study for Adults with First Episode/Early Phase Schizophrenia

Hello,

I wanted to let you know about a study that is taking place at our clinic. This study is sponsored by Vanguard

Research Group and our clinic is one of the research sites helping them with this study.

What is the purpose of this study?

Schizophrenia is a condition that negatively affects people’s mental health in different ways. For example, it can

affect a person’s mood, behavior, or cognition. Cobenfy is a new FDA approved drug for the treatment of the

positive symptoms of schizophrenia. Cobenfy is different from other antipsychotics as it has a new “mechanism

of action” compared to all other antipsychotics approved from the treatment of schizophrenia at this time. Since

Cobenfy is the first medication of its drug class to be FDA approved for schizophrenia, researchers are interested

to know how this new class of antipsychotics affects those with early phase schizophrenia specifically. This

clinical trial will test if Cobenfy can help improve the positive symptoms of patients with first episode/early

phase schizophrenia, better than other antipsychotics.

To be eligible to participate, you must:

❖ Be at least 18 years or older

❖ Have a primary diagnosis of schizophrenia

❖ Have been on a stable dose of 1 antipsychotic medication for at least 8 weeks before treatment with no

dose changes within the last 4 weeks.

❖ Have started your first antipsychotic treatment within the past 5 years.

Patients who meet eligibility criteria and enroll will come into our office to receive the study drug. Once

enrolled, in-person clinic visits will occur every 1-4 weeks for about 24 weeks until the end of treatment visit,

with a final follow-up visit 28 days after you last take the study drug (no more than 13 visits total).

If you decide to participate, the study drug will be provided by/paid for by our clinic and study related

assessments will be conducted during clinic visits. You may also be compensated for your participation and be

reimbursed for any study-related travel.

Want to learn more?

If you or someone you know is interested in learning more about this research study, please feel free to contact

us by calling 312-503-9092 or emailing.

Thank you for your time and I hope to hear from you soon.

Principal Investigator: Jeffrey Rado, MD

STU00223950

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