A Multicenter, Long-Term Open-Label Safety Study of Adjunctive Troriluzole in Subjects with Obsessive Compulsive Disorder
This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.
OCDDrug
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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Study ID: EUCTR 2020-004654-30. We help you review the study, but cannot decide medical eligibility.
Check recruitment and locations
EU CTR and CTIS records checked by HopeStage on . Registry information can change. Always confirm availability with the research team.
This study transferred to CTIS. HopeStage uses that newer record for the displayed status. A country's status does not guarantee that an individual site accepts participants.
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Italy · 4 sites
ASST Fatebenefratelli Sacco — Department of Biomedical and Clinical Sciences “L. Sacco”
Milan
Country status: Not recruiting
Ospedale San Raffaele S.r.l. — Mood Disorder Unit
Milan
Country status: Not recruiting
Azienda Ospedaliera Universitaria Federico II Di Napoli — Laboratory of Molecular Psychiatry at Department of Neuroscience
Naples
Country status: Not recruiting
Azienda Ospedaliero-Universitaria San Luigi Gonzaga — Department of Neurosciences
Orbassano
Country status: Not recruiting
Spain · 5 sites
Bellvitge University Hospital — Department of Psychiatry
L'hospitalet De Llobregat
Country status: Not recruiting
Hospital Universitario Ramon Y Cajal — Department of Psychiatry and Psychology
Madrid
Country status: Not recruiting
Hospital Universitario Central De Asturias — Department of Psychiatry
Oviedo
Country status: Not recruiting
Hospital Universitario De Salamanca — Department of Psychiatry
Salamanca
Country status: Not recruiting
Hospital Alvaro Cunqueiro — Department of Psychiatry
Vigo
Country status: Not recruiting
In plain English
Key information made simple
What the source confirms
This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.
What should you check before joining?
Check the official protocol for eligibility, treatment, visits and assessments. If recruitment is listed, confirm with the team that a specific centre is still accepting participants before taking any next step.
What to expect
Your next step
Study sites are listed in the registry. Recruitment status can differ between sites. Ask the research team to confirm the location, any in-person visits, time commitment, costs or compensation, and participation criteria.
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 dateNot clearly listed
Recruitment status
Not recruiting
Enrollment listed in the registry
1,200
Sponsor
Biohaven Pharmaceuticals, Inc
Sponsor type
Other organization
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
Italy, Spain
Age range
Not clearly listed
Official registry ID
EUCTR 2020-004654-30
Official title
A Multicenter, Long-Term Open-Label Safety Study of Adjunctive Troriluzole in Subjects with Obsessive Compulsive Disorder
This study may no longer be open, but we can help you understand it and find similar studies.
Study ID: EUCTR 2020-004654-30. We help you review the study, but cannot decide medical eligibility.
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 does the official source confirm?
This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.
Is this study recruiting?
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.
How can I check the participation requirements?
Check the official protocol for the criteria, treatment and planned assessments. The research team must confirm visits, risks, open centres and your eligibility.
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This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.
This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.