This study was terminated in the United States, in the United Kingdom, in Bulgaria, .... It is testing Efficacy of Lu AF35700 for schizophrenia.
SchizophreniaDrugOver 18 Years
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
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In plain English
Key information made simple
What is this study testing?
This study is testing whether the Efficacy of Lu AF35700 may be useful for adults experiencing schizophrenia.
What would participation involve?
Participants may receive the Efficacy of Lu AF35700, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in Bulgaria, in Japan, and in Russia.
Who is it mainly for?
This study appears to be mainly for adults with schizophrenia.
What should you check before joining?
Ask about the dose, safety monitoring, and possible side effects, whether there is placebo, randomization, or a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.
Your next step
Check the study details
Check the official source, then confirm these points with the research team.
Where are visits, can any be remote, and how much time is needed?
Costs and support
What costs, reimbursement or compensation apply?
Before joining
Questions to ask before joining
What are the exact eligibility criteria, and what could exclude someone?
How many visits, assessments, or follow-ups are expected, and over what period?
What risks, side effects, practical burdens, or alternatives should be understood first?
Who should be contacted to confirm locations, timing, compensation, and next steps?
Study clarity
Things to check before joining
Study start dateStarted: July 20, 2017
Recruitment status
Terminated
Enrollment listed in the registry
119
Sponsor
H. Lundbeck A/S
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Locations
United States, United Kingdom, Bulgaria, ...
Age range
Over 18 Years
Official registry ID
NCT03230864
Official title
Interventional, Randomized, Double-blind, Active-controlled Study of the Efficacy of Lu AF35700 in Patients With Early-in-disease or Late-in-disease Treatment-resistant Schizophrenia
Ask HopeStage to help me review this study
This record does not confirm open recruitment. We can help you understand it and explore other studies.
Study ID: NCT03230864. We help you review the study, but cannot decide medical eligibility.
Check recruitment and locations
Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability with the research team.
Tomsk National Research Medical Centre of the Russian Academy of Sciences
Tomsk
Site status: Not listed — confirm with the team
Yaroslavl Regional Clinical Psychiatric Hospital
Yaroslavl
Site status: Not listed — confirm with the team
Sverdlovsk Regional Clinical Psychiatric Hospital
Yekaterinburg
Site status: Not listed — confirm with the team
United Kingdom · 5 sites
Royal Edinburgh Hospital
Edinburgh
Site status: Not listed — confirm with the team
The Maudsley Hospital - GB0001
London
Site status: Not listed — confirm with the team
The Maudsley Hospital
London
Site status: Not listed — confirm with the team
Manchester Mental Health & Social Care NHS Trust - GB0003
Manchester
Site status: Not listed — confirm with the team
Manchester Mental Health & Social Care NHS Trust
Manchester
Site status: Not listed — confirm with the team
United States · 10 sites
University of California San Diego Health System
San Diego, California
Site status: Not listed — confirm with the team
Emory University Cognitive Neurology Clinic & ADRC
Atlanta, Georgia
Site status: Not listed — confirm with the team
Northwestern University
Chicago, Illinois
Site status: Not listed — confirm with the team
Corrigan Mental Health Center
Fall River, Massachusetts
Site status: Not listed — confirm with the team
University Of Massachusetts Medical Center
Worcester, Massachusetts
Site status: Not listed — confirm with the team
Michigan Clinical Research Institute PC
Ann Arbor, Michigan
Site status: Not listed — confirm with the team
Kalamazoo Community Mental Health and Substance Abuse Services
Kalamazoo, Michigan
Site status: Not listed — confirm with the team
PsychCare Consultants Research
St Louis, Missouri
Site status: Not listed — confirm with the team
Creighton University
Omaha, Nebraska
Site status: Not listed — confirm with the team
Psychiatric and Behavioral Solutions
Salt Lake City, Utah
Site status: Not listed — confirm with the team
In practice
For you
Participation may contribute to research. Personal benefit is not guaranteed.
Ask the research team to explain the activities, time commitment, and follow-up involved.
Study sites are listed. Confirm the relevant site and any travel before making plans.
Important
Not medical advice
Information from public sources.
Are you the study sponsor? Contact us to update this page: hi@hopestage.com
FAQ
Questions about this study
What is this study trying to understand?
This study is exploring medication or study treatment for people with schizophrenia. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.
Does this study involve a medication?
This appears to be a medication / drug study involving Lu AF35700, Risperidone, Olanzapine. Phase 3 studies are usually larger and aim to confirm effectiveness and safety in a broader group.
Who might this study be for?
This study may concern people with schizophrenia; age range: Over 18 Years. The criteria appear fairly broad, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.
What would I likely need to do?
You may need to take a study treatment and have regular medical follow-up. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.
What side effects, interactions, or treatment changes should I check?
If the study involves a medication, ask whether it is already approved, experimental, or being tested for a new use. Check possible side effects, interactions with current treatment, dose changes, monitoring, and what happens if you feel worse. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.
Will I need to travel or attend in-person visits?
The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.
Who is behind this study?
This study is sponsored by H. Lundbeck A/S, which appears to be unknown or unclear. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.
Can I still join this study?
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
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