- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: MDMA.
Displaying page 1 of 1.
| EudraCT Number: 2010-024543-33 | Sponsor Protocol Number: P64 | Start Date*: 2011-04-14 |
| Sponsor Name:Maastricht University | ||
| Full Title: Can memantine prevent memory impairment induced by MDMA in humans | ||
| Medical condition: none | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001718-13 | Sponsor Protocol Number: MP18 | Start Date*: 2019-10-18 |
| Sponsor Name:MAPS Europe B.V. | ||
| Full Title: An Open- Label, Phase 2, Multicenter Feasibility Study if Manualized MDMA-Assisted Psychotherapy with an fMRI sub-study Assessing Changes in Brain Activity in Subjects with Posttraumatic Stress Dis... | ||
| Medical condition: post-traumatic stress disorder (PTSD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) CZ (Completed) NO (Completed) DE (Completed) GB (GB - no longer in EU/EEA) ES (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-005596-39 | Sponsor Protocol Number: MPELONG | Start Date*: 2022-09-07 |
| Sponsor Name:MAPS Europe B.V. | ||
| Full Title: Long-Term Safety and Persistence of Effectiveness of Manualized MDMA Assisted Therapy for the Treatment of Posttraumatic Stress Disorder | ||
| Medical condition: post-traumatic stress disorder (PTSD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-000805-26 | Sponsor Protocol Number: PSYKFORSK_MAT-MDD | Start Date*: 2021-11-19 |
| Sponsor Name:Østfold Hospital Trust | ||
| Full Title: An Open-Label, Phase 2, Feasibility Study of Manualized MDMA-Assisted Psychotherapy in Subjects with Major Depressive Disorder | ||
| Medical condition: Major Depressive Disorder | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002547-42 | Sponsor Protocol Number: BIMA2016 | Start Date*: 2017-02-20 | |||||||||||
| Sponsor Name:Imperial College London, Joint Research Compliance Office | |||||||||||||
| Full Title: Open-Label Proof of Concept Feasibility Study to Explore the Safety, Tolerability and Potential Role of MDMA-Assisted Psychotherapy for the Treatment of Detoxified Patients with Alcohol Use Disorder. | |||||||||||||
| Medical condition: Alcohol Use Disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001169-26 | Sponsor Protocol Number: SNR-04 | Start Date*: 2019-05-02 | |||||||||||
| Sponsor Name:SyneuRx International (Taiwan) Corp | |||||||||||||
| Full Title: An Adaptive, Phase IIb/III, Multi-center, Prospective, Randomized, Double-Blind Placebo-controlled Study of the Safety and Efficacy of NaBen® (sodium benzoate), a D-Amino Acid Oxidase Inhibitor, as... | |||||||||||||
| Medical condition: Treatment for Schizophrenia in Adults | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001170-42 | Sponsor Protocol Number: SNR05 | Start Date*: 2019-07-12 |
| Sponsor Name:SyneuRx International (Taiwan) Corp | ||
| Full Title: An adaptive Phase II/III, Double-Blind, Randomized, Placebo-controlled, Two-Part, Dose-Finding, Multi-center Study of the Safety and Efficacy of NaBen® (sodium benzoate), a D-Amino Acid Oxidase In... | ||
| Medical condition: Treatment for Refractory Schizophrenia in Adults | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) GB (GB - no longer in EU/EEA) PL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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