- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Spatial orientation.
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EudraCT Number: 2005-003410-15 | Sponsor Protocol Number: 6251 7976 | Start Date*: 2005-11-21 |
Sponsor Name:Neurology Unit | ||
Full Title: A twelve-month double-blind placebo-controlled cross-over study of the effect ofAricept treatment on cognitive dysfunction in multiple sclerosis. | ||
Medical condition: Multiple sclerosis is a devastating inflammation in the central nervous system and it can often give cognitive dysfunction, affecting memory, mental concentration. Lately it has been shown that the... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002328-35 | Sponsor Protocol Number: CANTABRICO | Start Date*: 2020-11-11 | |||||||||||
Sponsor Name:AstraZeneca Farmacéutica Spain, S.A | |||||||||||||
Full Title: A Phase IIIB, Single Arm Study, of Durvalumab in Combination with Platinum-Etoposide for Untreated Patients with Extensive-Stage Small Cell Lung Cancer reflecting Real World Clinical Practice in Sp... | |||||||||||||
Medical condition: Extensive-Stage Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002454-20 | Sponsor Protocol Number: 35RC15_9724 | Start Date*: 2016-10-17 | |||||||||||
Sponsor Name:CHU de Rennes | |||||||||||||
Full Title: Apomorphine Pump in Early Stage of Parkinson’s Disease | |||||||||||||
Medical condition: Parkinson’s disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005263-16 | Sponsor Protocol Number: NSC15001 | Start Date*: 2016-07-11 | ||||||||||||||||
Sponsor Name:Pharmatrophix Inc | ||||||||||||||||||
Full Title: A 6-months prospective, multi-center, double-blind, placebo-controlled, randomized, adaptive-trial-design study to evaluate safety, tolerability and exploratory endpoints of either placebo or two d... | ||||||||||||||||||
Medical condition: Mild to moderate Alzheimer's disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) CZ (Completed) DE (Completed) SE (Completed) ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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