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TerminatedNCT00622245

Three Doses Lu AA34893 for depression

This study was terminated in Australia, in France, in Canada, .... It is testing Three Doses Lu AA34893 for depression.

Bipolarity, DepressionDrugFrom 18 Years to 65 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 Lu AA34893 may be useful for adults experiencing bipolarity.

What would participation involve?

Participants may receive Lu AA34893, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in Australia, in Austria, and in Belgium.

Who is it mainly for?

This study appears to be mainly for adults with bipolarity.

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 dateJanuary 2008
Recruitment status
Terminated
Enrollment listed in the registry
166
Sponsor
H. Lundbeck A/S
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
Australia, France, Canada, ...
Age range
From 18 Years to 65 Years
Official registry ID
NCT00622245
Official title
Randomised, Double-blind, Parallel-group, Placebo-controlled, and Active Referenced Study of Lu AA34893 to Evaluate the Efficacy and Safety of Three Doses Lu AA34893 in the Treatment of Depression in Patients With Bipolar I or II Disorder

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.

Australia · 3 sites
  • AU001
    Brisbane
    Site status: Not listed — confirm with the team
  • AU003
    Dandenong
    Site status: Not listed — confirm with the team
  • AU002
    Malvern
    Site status: Not listed — confirm with the team
Austria · 3 sites
  • AT002
    Vienna
    Site status: Not listed — confirm with the team
  • AT001
    Vienna
    Site status: Not listed — confirm with the team
  • AT003
    Vienna
    Site status: Not listed — confirm with the team
Belgium · 3 sites
  • BE004
    Brussels
    Site status: Not listed — confirm with the team
  • BE003
    Charleroi
    Site status: Not listed — confirm with the team
  • BE002
    Diest
    Site status: Not listed — confirm with the team
Bulgaria · 1 site
  • BG004
    Stara Zagora
    Site status: Not listed — confirm with the team
Canada · 3 sites
  • CA303
    London
    Site status: Not listed — confirm with the team
  • CA301
    Montreal
    Site status: Not listed — confirm with the team
  • CA302
    Orléans
    Site status: Not listed — confirm with the team
France · 4 sites
  • FR001
    Clermont-Ferrand
    Site status: Not listed — confirm with the team
  • FR007
    Orvault
    Site status: Not listed — confirm with the team
  • FR004
    Paris
    Site status: Not listed — confirm with the team
  • FR002
    Sartrouville
    Site status: Not listed — confirm with the team
Germany · 3 sites
  • DE004
    Berlin
    Site status: Not listed — confirm with the team
  • DE003
    Bochum
    Site status: Not listed — confirm with the team
  • DE002
    Gelsenkirchen
    Site status: Not listed — confirm with the team
Lithuania · 5 sites
  • LT005
    Kaunas
    Site status: Not listed — confirm with the team
  • LT003
    Kaunas Region
    Site status: Not listed — confirm with the team
  • LT004
    Klaipėda
    Site status: Not listed — confirm with the team
  • LT001
    Vilnius
    Site status: Not listed — confirm with the team
  • LT002
    Vilnius
    Site status: Not listed — confirm with the team
Malaysia · 3 sites
  • MY004
    Klang
    Site status: Not listed — confirm with the team
  • MY005
    Kota Kinabalu
    Site status: Not listed — confirm with the team
  • MY002
    Kuala Lumpur
    Site status: Not listed — confirm with the team
Philippines · 3 sites
  • PH002
    Las Piñas
    Site status: Not listed — confirm with the team
  • PH003
    Mandaluyong
    Site status: Not listed — confirm with the team
  • PH001
    Mandaue City
    Site status: Not listed — confirm with the team
Poland · 1 site
  • PL002
    Gdansk
    Site status: Not listed — confirm with the team
Romania · 4 sites
  • RO001
    Arad
    Site status: Not listed — confirm with the team
  • RO002
    Bucharest
    Site status: Not listed — confirm with the team
  • RO003
    Cluj-Napoca
    Site status: Not listed — confirm with the team
  • RO005
    Craiova
    Site status: Not listed — confirm with the team
Slovakia · 2 sites
  • SK001
    Bratislava
    Site status: Not listed — confirm with the team
  • SK002
    Prešov
    Site status: Not listed — confirm with the team
South Korea · 4 sites
  • KR004
    Inchon
    Site status: Not listed — confirm with the team
  • KR003
    Jeonju
    Site status: Not listed — confirm with the team
  • KR005
    Kyunggi-do
    Site status: Not listed — confirm with the team
  • KR002
    Seoul
    Site status: Not listed — confirm with the team
Sweden · 5 sites
  • SE006
    Halmstad
    Site status: Not listed — confirm with the team
  • SE003
    Lund
    Site status: Not listed — confirm with the team
  • SE005
    Malmö
    Site status: Not listed — confirm with the team
  • SE002
    Sollentuna
    Site status: Not listed — confirm with the team
  • SE001
    Stockholm
    Site status: Not listed — confirm with the team
Taiwan · 1 site
  • TW002
    Taichung
    Site status: Not listed — confirm with the team
Ukraine · 1 site
  • UA003
    Lviv
    Site status: Not listed — confirm with the team
United Kingdom · 1 site
  • GB001
    Oxford
    Site status: Not listed — confirm with the team

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.

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Study ID: NCT00622245. 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 is this study trying to understand?

This study is exploring medication or study treatment for people with bipolarity. 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 AA34893, Quetiapine fumarate, 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 bipolarity; age range: From 18 Years to 65 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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