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AVP-786 in the Treatment of Subjects with Agitation Associated with Dementia of the Alzheimer’s Type

Phase 1
Conditions
Agitation Associated with Dementia of the Alzheimer's Type
Therapeutic area: Diseases [C] - Nervous System Diseases [C10]
MedDRA version: 20.0 Level: PT Classification code 10001497 Term: Agitation System Organ Class: 10037175 - Psychiatric disorders
Registration Number
EUCTR2017-001339-38-FR
Lead Sponsor
Avanir Pharmaceuticals Inc.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
Not specified
Target Recruitment
412
Inclusion Criteria

1. Diagnosis of probable AD according to the 2011 NIA-AA working
groups criteria.
2. The patient has clinically significant, moderate/severe agitation at the
time of screening and for at least 2 weeks prior to randomization.
3. The diagnosis of agitation must meet the IPA provisional definition of agitation.
4. CGIS-Agitation score is = 4 (moderately ill) at Screening and Baseline.
5. MMSE score between 6 and 26 (inclusive) at Screening and Baseline.
6. Caregiver must be willing and able to comply with study procedures,including not administering any prohibited medications during the course of the study.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 103
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 309

Exclusion Criteria

1. Patient has dementia predominantly of non-Alzheimer's type (e.g.,
vascular dementia, frontotemporal dementia, Parkinson's disease,
substance-induced dementia).
2. Patients with symptoms of agitation that are not secondary to AD
(e.g., secondary to pain, other psychiatric disorder, or delirium).
3. Patients with myasthenia gravis (contraindication for quinidine).

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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