- Trials with a EudraCT protocol (306)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (49)
306 result(s) found for: TAU.
Displaying page 1 of 16.
| EudraCT Number: 2021-000473-83 | Sponsor Protocol Number: PET-tau-FACEHBI | Start Date*: 2021-12-15 |
| Sponsor Name:Fundació ACE-Institut Català de Neurociències Aplicades | ||
| Full Title: PET imaging study of the brain tau deposit in individuals with subjective cognitive decline and mild cognitive impairment: FACEHBI cohort. | ||
| Medical condition: Subjective cognitive impairment and mild cognitive decline in evaluation for diagnosis of Alzheimer's Disease. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-004634-41 | Sponsor Protocol Number: IIBSP-FPI-2019-108 | Start Date*: 2021-08-25 |
| Sponsor Name:Institut de Recerca HSCSP | ||
| Full Title: Study of the positron emission tomography (PET) tracer for tau 18F-PI-2620 in individuals with Down syndrome | ||
| Medical condition: Taupathies | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004466-34 | Sponsor Protocol Number: 18-07 | Start Date*: 2019-05-16 |
| Sponsor Name:Amsterdam UMC VUmc | ||
| Full Title: Tau PET imaging in cognitively normal elderly subjects: A twin approach | ||
| Medical condition: Cognitively healthy elderly, aged 60-100 years old. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-003473-94 | Sponsor Protocol Number: UCL-2016-121 | Start Date*: 2019-05-20 |
| Sponsor Name:Cliniques Universitaires Saint-Luc | ||
| Full Title: Tau and Amyloid PET imaging in normal aging, early Alzheimer's disease and related syndroms. | ||
| Medical condition: Alzheimer’s disease (AD) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-004290-84 | Sponsor Protocol Number: tau-PET/BBRC2019 | Start Date*: 2020-04-29 |
| Sponsor Name:BarcelonaBeta Brain Research Center | ||
| Full Title: Characterization of cerebral tau aggregates with 18F-RO6958948 PET in the ALFA population. | ||
| Medical condition: Alzheimer's Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001257-27 | Sponsor Protocol Number: S61444 | Start Date*: 2018-05-22 |
| Sponsor Name:KU Leuven | ||
| Full Title: Cognitive brain circuits and the spread of tau in vivo in humans | ||
| Medical condition: Alzheimer disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-003733-15 | Sponsor Protocol Number: B-003 | Start Date*: 2013-11-13 |
| Sponsor Name:VU University medical center | ||
| Full Title: The Dutch CSF and PET Biomarker Concordance of Alzheimer’s Disease pathology study | ||
| Medical condition: Patients visiting the VUmc Alzheimer Center with objective cognitive complaints or diagnosed with Alzheimer's Disease. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-002511-22 | Sponsor Protocol Number: 20-05 | Start Date*: 2023-06-08 |
| Sponsor Name:Amsterdam UMC VUmc | ||
| Full Title: Synaptic density and tau pathology in Alzheimer's disease | ||
| Medical condition: Amyloid-beta positive individuals across the Alzheimer's disease continuum | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-003891-11 | Sponsor Protocol Number: LMT-01-02-18 | Start Date*: 2019-07-16 | |||||||||||
| Sponsor Name:Life Molecular Imaging SA | |||||||||||||
| Full Title: An Open Label, Single Center Study, to evaluate the Safety and Imaging Characteristics of [18F]PI-2620 as PET Radioligand for Imaging Tau deposition in the brains of subjects with amnestic mild cog... | |||||||||||||
| Medical condition: Alzheimer's Disease Amnestic Mild Cognitive Impairment | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000978-35 | Sponsor Protocol Number: STOP-SPG5 | Start Date*: 2015-10-21 |
| Sponsor Name:University Hospital Tübingen | ||
| Full Title: Statin Treatment of Oxysterol Pathology in SPG5: a Randomized Controlled Trial -Proof of Principle | ||
| Medical condition: SPG5 | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-001114-14 | Sponsor Protocol Number: ST261-DS-02-002 | Start Date*: 2004-10-22 |
| Sponsor Name:SIGMA-TAU | ||
| Full Title: BIOAVAILABILITY AND BIOEQUIVALENCE OF TWO ORAL FORMULATION OF L-PROPIONYLCARNITINE TABLET VS SACHET IN HEALTHY VOLUNTEERS AT THE DOSE OF 2 G OPEN, RANDOMISED, TWO-WAYS CROSS-OVER, SINGLE DOSE STUDY | ||
| Medical condition: BIOEQUIVALENCE /BIOAVAILABILITY STUDY | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male | |
| Trial protocol: IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-002223-28 | Sponsor Protocol Number: PHAO14-CH/TEPTAU | Start Date*: 2016-11-30 |
| Sponsor Name:CHRU DE TOURS | ||
| Full Title: Tau brain imaging in typical and atypical Alzheimer’s Disease (AD) | ||
| Medical condition: Alzheimer's diseases | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-004816-39 | Sponsor Protocol Number: CA012-004 | Start Date*: 2016-08-11 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Phase 1/2a Study of BMS-986178 Administered Alone and in Combination with Nivolumab or Ipilimumab in Advanced Solid Tumors | |||||||||||||
| Medical condition: Advanced Solid Tumors | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) NL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-004656-22 | Sponsor Protocol Number: IIBSP-THK-2015-77 | Start Date*: 2017-10-10 |
| Sponsor Name:Institut de Recerca HSCSP | ||
| Full Title: Pilot study of the [18F]THK-5351 positron emission tomography (PET) tracer in different tauopathies. | ||
| Medical condition: Taupatías | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-001336-22 | Sponsor Protocol Number: AX-PC-201 | Start Date*: 2004-11-03 |
| Sponsor Name:Axonyx Inc. | ||
| Full Title: Effect of Phenserine Treatment on Amyloid in Brains of Patients with Mild Probable Alzheimer’s Disease as studied by Positron Emission Tomography (PET). A Randomised, three Months Double-Blind, Pla... | ||
| Medical condition: Alzheimer’s Disease (AD) is the most common disease leading to dementia and it affects approximately 4 to 8% of the population aged above 65 years. The disease incidence is closely correlated with ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-000970-31 | Sponsor Protocol Number: TUD-ASLith-057 | Start Date*: 2013-11-27 | |||||||||||
| Sponsor Name:Technische Universität Dresden | |||||||||||||
| Full Title: Randomized, placebo-controlled multicenter trial of lithium plus treatment as usual (TAU) for acute suicidal ideation and behaviour in patients with suicidal major depressive episode | |||||||||||||
| Medical condition: Diagnosis of a major depressive episode; inpatient at screening visit; suicidal ideation/behaviour present defined by a clinical rating of ≥ 8 on the Sheehan Suicidality Tracking Scale (S-STS) at... | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003763-56 | Sponsor Protocol Number: ST3073-ST3074-DM13-001 | Start Date*: 2014-01-09 | |||||||||||
| Sponsor Name:Sigma-Tau Industrie Farmaceutiche Riunite S.p.A. | |||||||||||||
| Full Title: Proof of Concept Study of Eurartesim® in Patients with Imported Uncomplicated Plasmodium Vivax Malaria | |||||||||||||
| Medical condition: Patients affected by uncomplicated Plasmodium vivax malaria | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) ES (Completed) NL (Completed) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-002226-11 | Sponsor Protocol Number: SIMaMCI | Start Date*: 2008-10-07 |
| Sponsor Name:Charité - Unversitätsmedizin Berlin | ||
| Full Title: Randomized Controlled Trial of Simvastatin in Amnestic MCI Patients | ||
| Medical condition: Amnestic mild cognitive impairment (MCI) denotes clinical conditions in the border zone between normal cognitive functioning and dementia. The definition of amnestic MCI by Petersen and his co-work... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-004244-28 | Sponsor Protocol Number: BAN2401-G000-303 | Start Date*: 2023-04-17 | |||||||||||
| Sponsor Name:Eisai Ltd. | |||||||||||||
| Full Title: AHEAD 3-45 Study: A Placebo-Controlled, Double-Blind, Parallel Treatment Arm, 216 Week Study with an Extension Phase to Evaluate Efficacy and Safety of Treatment With BAN2401 in Subjects With Prec... | |||||||||||||
| Medical condition: Preclinical Alzheimer's Disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000116-30 | Sponsor Protocol Number: 63733657ALZ2002 | Start Date*: 2021-04-07 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Assess the Efficacy and Safety of JNJ-63733657, an Anti-tau Monoclonal Antibody, in Participants with Early Alzh... | |||||||||||||
| Medical condition: Early Alzheimer’s Disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) FR (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.