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Drug Use-results survey for Reminyl 4mg/8mg/12mg Tablets, 4mg/8mg/12mg OD Tablets, 4mg/mL Oral Solution

Drug Use-results survey for Reminyl 4mg/8mg/12mg Tablets, 4mg/8mg/12mg OD Tablets, 4mg/mL Oral Solution - Drug Use-results survey for Reminyl 4mg/8mg/12mg Tablets, 4mg/8mg/12mg OD Tablets, 4mg/mL Oral Solution

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000015897
Enrollment
1900
Registered
2014-12-15
Start date
2011-05-16
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild to moderately severe dementia of the Alzheimer&#39

Interventions

None listed

Sponsors

Janssen Pharmaceutical K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with mild to moderately severe dementia of the Alzheimer's type

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Safety(Adverse drug reactions) Effectiveness (Clinical Global Impression-Improvement scale)

Countries

Japan

Contacts

Public ContactHirokazu Shirai

Janssen Pharmaceutical K.K. Safety Risk Management Dept.

hshirai3@ITS.JNJ.com03-4411-5951

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026