Efficacy of ORM-12741 on Agitation/Aggression Symptoms in Alzheimer's Disease

NCT ID: NCT02471196

Last Updated: 2018-02-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 308 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-08-14
• Study Completion Date: 2017-12-04

Brief Summary

This study evaluates the effect of ORM-12741 on agitation/aggression symptoms in Alzheimer's disease. Two thirds of the patients will receive ORM-12741 and one third will receive placebo.

Detailed Description

ORM-12741 is a potent and selective alpha-2C adrenoceptor (AR)-antagonist. Previous results suggest that the compound may have positive effects on both cognitive and neuropsychiatric symptoms of Alzheimer's Disease. In this study, the effect of ORM-12741 will be evaluated on agitation/aggression symptoms and other neuropsychiatric symptoms. Furthermore, cognition and psychotic and depressive symptoms will be evaluated.

Conditions

Alzheimer's Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

ORM-12741 low dose

ORM-12741 low dose twice a day for 12 weeks.

Group Type: EXPERIMENTAL

ORM-12741

Intervention Type: DRUG

ORM-12741 low dose twice a day

ORM-12741 high dose

ORM-12741 high dose twice a day for 12 weeks.

Group Type: EXPERIMENTAL

ORM-12741

Intervention Type: DRUG

ORM-12741 high dose twice a day

Placebo

Placebo twice a day for 12 weeks.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Placebo twice a day

Interventions

ORM-12741

ORM-12741 low dose twice a day

Intervention Type: DRUG

ORM-12741

ORM-12741 high dose twice a day

Intervention Type: DRUG

Placebo

Placebo twice a day

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Written informed consent (IC) for participation in the study (co-signed by the subject's next of kin or caregiver, or other legally acceptable representative.
• Written IC obtained from a consistently available caregiver informant who is knowledgeable of the subject's condition and its progression and is willing to accompany the subject to all visits and supervise the administration of the study medication.
• Age of 55-90 years (inclusive).
• Male or female subjects with diagnosis of probable Alzheimer's Disease.
• Brain imaging (computed tomography [CT] or magnetic resonance imaging [MRI]) consistent with a diagnosis of Alzheimer's Disease (within 18 months or at screening).
• Mini-mental state examination (MMSE) score between 10-24 (inclusive).
• Clinically significant agitation meeting the International Psychogeriatric Association Provisional Criteria for Agitation in Cognitive Impairment. The agitation symptoms need to have been present for at least 4 weeks before the screening visit.
• Neuropsychiatric Inventory agitation/aggression item score at least 4 at screening visit.

Exclusion Criteria

• Modified Hachinski Ischemia Score (MHIS) > 4.
• Changes in AChE inhibitor (donepezil, rivastigmine or galantamine) dosing within 2 months prior to screening.
• Changes in memantine dosing within 2 months prior to the screening.
• Changes in antidepressant dosing or addition of another antidepressant medication within 2 months prior to the screening.
• Use of antipsychotics at any dose within 1 month prior to screening.
• Use of benzodiazepines, other than short-acting sleep medications, for night at a maximum of 3 nights/week, within 2 months prior to screening.
• Use of any anticholinergic medication within 2 months prior to screening.
• Current use (within the 30 days prior to screening) of medications with known relevant alpha-2C AR affinity (e.g. mirtazapine, mianserin, clonidine, guanfacine or tizanidine) or with high noradrenaline transporter affinity (reboxetine, venlafaxine or duloxetine).
• Current use of other psychotropic agents, unless the dosing has been stable during the last 2 months prior to the screening.
• Myocardial infarction or other clinically significant ischemic cardiac disease, heart failure, or arrhythmia tendency within the past 2 years.
• Current or history of malignancy within 5 years before screening.
• Suicidal ideation in the 6 months before screening or current suicide risk based on the Colombia-Suicide Severity Rating Scale (C-SSRS) (items 4 and 5 exclusionary) or current risk of suicide based on the investigator's judgement.
• Specific findings in MRI or CT that could in the opinion of the investigator affect cognitive function (such as cortical infarct or silent lacuna in a region known to affect cognition).
• Supine heart rate < 48 bpm or > 100 bpm.
• Systolic blood pressure (SBP) > 160 mmHg or diastolic blood pressure (DBP) > 100 mmHg after a 5-minute rest.
• Symptomatic orthostatic hypotension.
• QTc-Fridericia (QTcF) repeatedly > 450 ms in males or > 470 ms in females.
• Clinically significantly abnormal thyroid-stimulating hormone (TSH), vitamin B12 or folate serum levels at screening.
• Resides in a skilled nursing facility.

• Minimum Eligible Age: 55 Years
• Maximum Eligible Age: 90 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Janssen Pharmaceuticals

INDUSTRY

Sponsor Role: collaborator

Orion Corporation, Orion Pharma

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Juha Rinne, Prof

Role: PRINCIPAL_INVESTIGATOR

Clinical Research Services Turku - CRST Oy

Locations

Clinical Research Services Turku - CRST Oy

Turku, , Finland

Countries

Finland

Other Identifiers

3098012

Identifier Type: -

Identifier Source: org_study_id