- Trials with a EudraCT protocol (49)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
49 result(s) found for: Depressive Disorder, Treatment-Resistant AND Depression.
Displaying page 1 of 3.
EudraCT Number: 2018-004208-20 | Sponsor Protocol Number: GH001-MDD-102 | Start Date*: 2019-08-21 | |||||||||||||||||||||
Sponsor Name:Gh Research Limited | |||||||||||||||||||||||
Full Title: A phase 1/2 study of GH001 in patients with treatment-resistant depression | |||||||||||||||||||||||
Medical condition: Treatment-resistant depression | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-006089-40 | Sponsor Protocol Number: 2006TUDOR_01 | Start Date*: 2007-03-20 | |||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | |||||||||||||
Full Title: High dose corticosteroid pulses in treatment-resistant depression : a randomized double-blind placebo-controlled pilot study | |||||||||||||
Medical condition: Resistant depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002160-24 | Sponsor Protocol Number: BP25712 | Start Date*: 2012-04-12 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | ||||||||||||||||||
Full Title: A Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Investigate the Efficacy and Safety of RO4995819 Versus Placebo, as Adjunctive Therapy in Patients with Major D... | ||||||||||||||||||
Medical condition: Major Depressive Disorder | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) DE (Completed) SK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-005457-25 | Sponsor Protocol Number: PCN-101-21 | Start Date*: 2021-08-30 | |||||||||||
Sponsor Name:Perception Neuroscience, Inc | |||||||||||||
Full Title: A randomized, placebo-controlled, double-blind study to assess the safety and efficacy of intravenous PCN-101 in treatment-resistant depression | |||||||||||||
Medical condition: Treatment-resistant depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001637-27 | Sponsor Protocol Number: LQD | Start Date*: 2016-09-20 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:South London and Maudsley NHS Foundation Trust [...] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomised pragmatic trial comparing the clinical and cost effectiveness of lithium and quetiapine augmentation in treatment resistant depression. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Treatment resistant major depressive disorder (single episode or recurrent). Treatment resistant depression, defined as failure to respond to two or more adequate doses of antidepressant in the cur... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002577-22 | Sponsor Protocol Number: COMP003 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:COMPASS Pathfinder, Limited | ||||||||||||||||||
Full Title: The safety and efficacy of psilocybin as an adjunctive therapy in participants with treatment-resistant depression | ||||||||||||||||||
Medical condition: treatment resistant depression | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003288-36 | Sponsor Protocol Number: COMP001 | Start Date*: 2018-03-09 | ||||||||||||||||
Sponsor Name:COMPASS Pathways, Ltd | ||||||||||||||||||
Full Title: The Safety and Efficacy of Psilocybin in Participants with Treatment Resistant Depression (P-TRD) | ||||||||||||||||||
Medical condition: Treatment-Resistant Depression (P-TRD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) DE (Completed) PT (Completed) NL (Completed) IE (Completed) DK (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004005-11 | Sponsor Protocol Number: ESKETINTRD2003 | Start Date*: 2013-12-17 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Double-Blind, Doubly-Randomized, Placebo-Controlled Study of Intranasal Esketamine in an Adaptive Treatment Protocol to Assess Safety and Efficacy in Treatment-Resistant Depression (SYNAPSE) | |||||||||||||
Medical condition: Treatment Resistant Major Depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000574-26 | Sponsor Protocol Number: GH001-TRD-201 | Start Date*: 2022-11-25 | |||||||||||
Sponsor Name:GH Research Ireland Limited | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, Phase 2b trial with an open-label extension to determine the safety and efficacy of GH001 in patients with treatment-resistant depression | |||||||||||||
Medical condition: Treatment-resistant depression (TRD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Trial now transitioned) CZ (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006510-36 | Sponsor Protocol Number: NL79264.091.21 | Start Date*: 2021-12-21 | |||||||||||
Sponsor Name:Radboudumc | |||||||||||||
Full Title: Exploring the Pharmacomicrobiomics of Depression | |||||||||||||
Medical condition: Major Depressive Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000778-71 | Sponsor Protocol Number: CN162-007 | Start Date*: 2011-11-15 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Active Controlled, Comparative, Fixed-Dose, Dose Response Study of the Efficacy and Safety of BMS-820836 in Patients with Treatment Resistant Major Depress... | |||||||||||||
Medical condition: Subjects with Treatment Resistant Major Depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) AT (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000908-91 | Sponsor Protocol Number: D1443L00044 | Start Date*: 2008-10-16 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A randomised, 6-week, multicentre, open-label, rater-blinded parallelgroup study comparing Quetiapine extended release monotherapy and augmentation with Lithium augmentation in patients with Treatm... | |||||||||||||
Medical condition: Treatment resistant depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SK (Completed) AT (Completed) HU (Completed) DK (Prematurely Ended) BE (Completed) GB (Completed) IT (Completed) PT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024371-12 | Sponsor Protocol Number: CN162-010 | Start Date*: 2011-11-15 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A multicenter, Double-blind 58 week Rollover Study to assess the Safety and Tolerability of BMS-820836 in Patients with Treatment Resistant Major Depression. | |||||||||||||
Medical condition: Subjects with Treatment Resistant Major Depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Temporarily Halted) SE (Completed) FI (Prematurely Ended) AT (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003196-35 | Sponsor Protocol Number: 13HH0762 | Start Date*: 2015-01-07 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: Assessing the subjective intensity of oral psilocybin in patients with treatment-resistant depression: A Pilot Study | |||||||||||||
Medical condition: Major depressive disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004169-28 | Sponsor Protocol Number: SC17.02 | Start Date*: 2018-06-21 | |||||||||||
Sponsor Name:I.R.C.C.S. FONDAZIONE S.LUCIA | |||||||||||||
Full Title: Augmentation versus switch: comparative effectiveness research trial for antidepressant incomplete and non-responders with treatment resistant depression | |||||||||||||
Medical condition: Non-responders with Treatment Resistant Depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002232-16 | Sponsor Protocol Number: TAK-653-2001 | Start Date*: 2017-12-15 | |||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc, a wholly owned subsidiary of Takeda Pharmaceutical Company, Ltd | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of TAK-653 in the Treatment of Subjects with Treatment-Resistant Depression | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022841-93 | Sponsor Protocol Number: CN162-006 | Start Date*: 2011-07-08 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Active-Controlled Study of the Efficacy and Safety of Flexibly-Dosed BMS-820836 in Patients with Treatment Resistant Major Depression Revised protocol ... | |||||||||||||
Medical condition: Subjects with Treatment Resistant Major Depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000090-23 | Sponsor Protocol Number: UoB1651 | Start Date*: 2013-06-19 | |||||||||||
Sponsor Name:University of Bristol | |||||||||||||
Full Title: Mirtazapine added to SSRIs for treatment resistant depression in primary care: a placebo controlled randomised controlled trial | |||||||||||||
Medical condition: Treatment resistant depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004584-20 | Sponsor Protocol Number: ESKETINTRD3001 | Start Date*: 2015-09-16 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Multicenter, Active-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Fixed Doses of Intranasal Esketamine Plus an Oral Antidepressant in Adult Subj... | |||||||||||||
Medical condition: Treatment-resistant Major Depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SK (Completed) HU (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004588-19 | Sponsor Protocol Number: ESKETINTRD3005 | Start Date*: 2015-08-04 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Randomized, Double-blind, Multicenter, Active-controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Intranasal Esketamine Plus an Oral Antidepressant in Elderly Subjects with Tre... | |||||||||||||
Medical condition: Treatment-resistant Major Depression | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) BE (Completed) ES (Completed) GB (Completed) LT (Completed) FI (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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