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CompletedNCT02151656

F17464 in Acute Schizophrenia study

This study is completed. It focuses on schizophrenia and currently lists study information in France, Hungary, Latvia, Romania, and Russian Federation.

SchizophreniaDrugFrom 18 Years to 64 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.

Then choose your country and confirm availability with each study site.

In plain English

Key information made simple

What is this study testing?

This study is testing whether F17464 may be useful for adults experiencing schizophrenia.

What would participation involve?

Participants may receive F17464, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in France, in Hungary, and in Latvia.

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.

View official study record (opens in a new tab)
  • Recruitment and eligibility

    Is a site open, and who can take part?

  • Visits and time

    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

Study clarity

Things to check before joining

Study start dateJune 2014
Recruitment status
Completed
Enrollment listed in the registry
158
Sponsor
Pierre Fabre Medicament
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
France, Hungary, Latvia, ...
Age range
From 18 Years to 64 Years
Official registry ID
NCT02151656
Official title
Effects of F17464 in Acute Exacerbation of Schizophrenia

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Study ID: NCT02151656. 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.

View official study record (opens in a new tab)

The overall study status can differ from each site's status. Open a country to see its locations and their registry status.

France · 2 sites
  • Nîmes
    Nîmes
    Site status: Not listed — confirm with the team
  • Sotteville-lès-Rouen
    Sotteville-lès-Rouen
    Site status: Not listed — confirm with the team
Hungary · 3 sites
  • Balassagyarmat
    Balassagyarmat
    Site status: Not listed — confirm with the team
  • Budapest
    Budapest
    Site status: Not listed — confirm with the team
  • Gyula
    Gyula
    Site status: Not listed — confirm with the team
Latvia · 4 sites
  • Daugavpils
    Daugavpils
    Site status: Not listed — confirm with the team
  • Jelgava
    Jelgava
    Site status: Not listed — confirm with the team
  • Liepāja
    Liepāja
    Site status: Not listed — confirm with the team
  • Strenči
    Strenči
    Site status: Not listed — confirm with the team
Romania · 10 sites
  • Arad
    Arad
    Site status: Not listed — confirm with the team
  • Bucharest
    Bucharest
    Site status: Not listed — confirm with the team
  • Campulum G Muscel
    Campulum G Muscel
    Site status: Not listed — confirm with the team
  • Craiova
    Craiova
    Site status: Not listed — confirm with the team
  • Galati
    Galati
    Site status: Not listed — confirm with the team
  • Iași
    Iași
    Site status: Not listed — confirm with the team
  • Sibiu
    Sibiu
    Site status: Not listed — confirm with the team
  • Targoviste
    Targoviste
    Site status: Not listed — confirm with the team
  • Târgu Mureş
    Târgu Mureş
    Site status: Not listed — confirm with the team
  • Timișoara
    Timișoara
    Site status: Not listed — confirm with the team
Russia · 8 sites
  • Arkhangelsky District
    Arkhangelsky District
    Site status: Not listed — confirm with the team
  • Engel's
    Engel's
    Site status: Not listed — confirm with the team
  • Kazan'
    Kazan'
    Site status: Not listed — confirm with the team
  • Moscow
    Moscow
    Site status: Not listed — confirm with the team
  • Orenburg
    Orenburg
    Site status: Not listed — confirm with the team
  • Saratov
    Saratov
    Site status: Not listed — confirm with the team
  • Tomsk
    Tomsk
    Site status: Not listed — confirm with the team
  • Yekaterinburg
    Yekaterinburg
    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 F17464, Placebo. Phase 2 studies usually explore whether the intervention may work, while continuing to monitor safety.

Who might this study be for?

This study may concern people with schizophrenia; age range: From 18 Years to 64 Years. The criteria appear fairly specific, 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 Pierre Fabre Medicament, 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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