WHO ICTRP trial
Efficacy and safety of S 38093 versus placebo, in co-administration with…
EUCTR2011-005862-40-DE · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2011-005862-40-DE |
|---|---|
| Public title | Efficacy and safety of S 38093 versus placebo, in co-administration with donepezil in patients with moderate Alzheimer's Disease |
| Scientific title | Efficacy and safety of 3 doses of S 38093 (2, 5 and 20 mg/day) versus placebo, in co-administration with donepezil (10 mg/day) in patients with moderate Alzheimer’s Disease. A 24-week international, multi-centre, randomised, double-blind, placebo-controlled phase IIb study. |
| Primary sponsor | Institut de Recherches Internationales Servier |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Countries | Portugal;Slovakia;Finland;Spain;Austria;United Kingdom;Italy;Mexico;Canada;Argentina;Brazil;Poland;Australia;Germany;Sweden |
| Conditions | moderate Alzheimer's disease MedDRA version: 17.0 Level: LLT Classification code 10001896 Term: Alzheimer's disease System Organ Class: 100000004852 ;Therapeutic area: Diseases [C] - Nervous System Diseases [C10] |
| Interventions | Product Name: S38093 Product Code: S38093-2 Pharmaceutical Form: Film-coated tablet INN or Proposed INN: S38093 Current Sponsor code: S38093-2 Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 2… |
| Registration date | Jan 6, 2012 |
| Target size | 700 |
| Secondary IDs | CL2-38093-012 |
| Registry page | clinicaltrialsregister.eu |
At a glance
- No Results available
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: