- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Manic and bipolar mood disorders and disturbances.
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| EudraCT Number: 2017-000803-25 | Sponsor Protocol Number: RGH-MD-25 | Start Date*: 2019-10-02 | ||||||||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | ||||||||||||||||||
| Full Title: A DOUBLE-BLIND, PLACEBO-CONTROLLED, RANDOMIZED WITHDRAWAL, MULTICENTER CLINICAL TRIAL EVALUATING THE EFFICACY, SAFETY, AND TOLERABILITY OF CARIPRAZINE IN A DOSE-REDUCTION PARADIGM IN THE PREVENTION... | ||||||||||||||||||
| Medical condition: Bipolar I disorder | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BG (Completed) RO (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-006861-39 | Sponsor Protocol Number: GH001-BD-202 | Start Date*: 2022-06-20 | |||||||||||
| Sponsor Name:GH Research Ireland Limited | |||||||||||||
| Full Title: A Phase 2 Clinical Trial of GH001 in Patients with Bipolar II Disorder and a Current Major Depressive Episode (GH001-BD-202) | |||||||||||||
| Medical condition: Bipolar II Disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-023992-24 | Sponsor Protocol Number: MEMAP1 | Start Date*: 2011-08-26 | |||||||||||
| Sponsor Name:University of Leipzig | |||||||||||||
| Full Title: International randomised double-blind placebo-controlled study on the initial treatment of acute mania with methylphenidate | |||||||||||||
| Medical condition: acute mania and hypomania (ICD-10: F30.0, F30.1, F31.0, F31.1) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Prematurely Ended) BE (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012003-26 | Sponsor Protocol Number: RIS-NAP-4022 | Start Date*: 2010-04-13 | |||||||||||||||||||||
| Sponsor Name:Janssen-Cilag International, NV | |||||||||||||||||||||||
| Full Title: Evaluation of Growth, Sexual Maturation, and Prolactin-Related Adverse Events in the Pediatric Population Exposed to Atypical Antipsychotic Drugs | |||||||||||||||||||||||
| Medical condition: Long-term safety data in children and adolescents will be collected from a population of patients with a diagnosis of schizophrenia, bipolar mania, autistic disorder or conduct and other disruptive... | |||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Prematurely Ended) BE (Prematurely Ended) GR (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2006-005734-20 | Sponsor Protocol Number: R076477-SCA-3002 | Start Date*: 2008-04-24 | |||||||||||
| Sponsor Name:Janssen L.P. | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy and Safety of Flexible Dose Paliperidone ER in the Treatment of Subjects with Schizoaffective Disorder | |||||||||||||
| Medical condition: Schizoaffective disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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Query did not match any studies.