WHO ICTRP trial
A 76-week prospective, open-label, multicenter study to evaluate the long-term…
EUCTR2007-000350-31-FR · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2007-000350-31-FR |
|---|---|
| Public title | A 76-week prospective, open-label, multicenter study to evaluate the long-term effect of Exelon® capsule and transdermal patch on worsening of the underlying motor symptoms of PD in patients with mild to moderately severe dementia associated with Parkinson’s disease (PDD). |
| Scientific title | A 76-week prospective, open-label, multicenter study to evaluate the long-term effect of Exelon® capsule and transdermal patch on worsening of the underlying motor symptoms of PD in patients with mild to moderately severe dementia associated with Parkinson’s disease (PDD). |
| Primary sponsor | Novartis Pharma AG |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Countries | France;Spain;Italy |
| Conditions | Mild to moderately severe dementia associated with Parkinson’s disease (PDD). MedDRA version: 9.1 Level: LLT Classification code 10012284 Term: Dementia due to Parkinson's disease |
| Interventions | Trade Name: Exelon Pharmaceutical Form: Capsule, hard INN or Proposed INN: rivastigmine Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 1.5- Trade Name: Exelon Pharmaceutical Form: Capsule, hard INN or… |
| Registration date | Oct 25, 2007 |
| Target size | 550 |
| Secondary IDs | CENA713B2315 |
| Registry page | clinicaltrialsregister.eu |
At a glance
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: