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Not recruitingEUCTR 2022-003743-10

A Quadruple Masked, Dose-Finding Study to Evaluate the Efficacy and Safety of Intranasal BPL-003, with Open Label Extension, in Patients with Treatment Resistant Depression

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.

DepressionDrug

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 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.

Your next step

Check the study details

Check the official source, then confirm these points with the research team.

View the historical EU CTR 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 dateNot clearly listed
Recruitment status
Not recruiting
Enrollment listed in the registry
203
Sponsor
Beckley Psytech Ltd.
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
Germany, Poland, Spain
Age range
Not clearly listed
Official registry ID
EUCTR 2022-003743-10
Official title
A Quadruple Masked, Dose-Finding Study to Evaluate the Efficacy and Safety of Intranasal BPL-003, with Open Label Extension, in Patients with Treatment Resistant Depression

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.

View the historical EU CTR record (opens in a new tab)View the current CTIS record (opens in a new tab)
Current CTIS country statuses
Historical EU CTR country statuses

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

Germany · 5 sites
  • Charite Universitaetsmedizin Berlin KöR — Psychiatry and Neurosciences
    Berlin
    Country status: Not recruiting
  • OVID Clinic Berlin GmbH — Medical Direction
    Berlin
    Country status: Not recruiting
  • Universitätsklinikum Frankfurt — Psychosomatik und Psychotherapie
    Frankfurt am Main
    Country status: Not recruiting
  • Zentralinstitut Fuer Seelische Gesundheit — Molecular Neuroimaging
    Mannheim
    Country status: Not recruiting
  • Universitaetsklinikum Tuebingen AöR — Klinik für Psychiatrie und Psychotherapie
    Tuebingen
    Country status: Not recruiting
Poland · 5 sites
  • Centrum Badan Klinicznych Pi-House Sp. z o.o. — N/A
    Gdansk
    Country status: Not recruiting
  • Uniwersyteckie Centrum Kliniczne — Klinika Psychiatrii Dorosłych
    Gdansk
    Country status: Not recruiting
  • Samodzielny Publiczny Zaklad Opieki Zdrowotnej Centralny Szpital Kliniczny Uniwersytetu Medycznego W Lodzi — Klinika Zaburzeń Afektywnych i Psychotycznych
    Lodz
    Country status: Not recruiting
  • Inventiva Biomedical And Research Sp. z o.o. — N/A
    Tuszyn
    Country status: Not recruiting
  • Instytut Psychiatrii I Neurologii — Zakład Farmakologii i Fizjologii Układu Nerwowego
    Warsaw
    Country status: Not recruiting
Spain · 6 sites
  • Hospital Clinic De Barcelona — -
    Barcelona
    Country status: Not recruiting
  • Hospital Del Mar — -
    Barcelona
    Country status: Not recruiting
  • Hospital Sant Joan De Deu Barcelona — -
    Esplugues De Llobregat
    Country status: Not recruiting
  • Hospital Universitario Hm Puerta Del Sur — -
    Mostoles
    Country status: Not recruiting
  • Centro de Salud Mental La Corredoria — -
    Oviedo
    Country status: Not recruiting
  • Hospital Universitario De Salamanca — -
    Salamanca
    Country status: Not recruiting

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Study ID: EUCTR 2022-003743-10. 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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