Nuedexta in the Treatment of Pseudobulbar Affect in Patients With Alzheimer's Disease

NCT ID: NCT01832350

Last Updated: 2019-10-29

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE4
• Total Enrollment: 34 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-08-28
• Study Completion Date: 2016-12-01

Brief Summary

The primary objective of this study is to test the hypothesis that Nuedexta (20/10) administered orally will reduce Pseudobulbar Affect (PBA) frequency and severity (CNS-Lability Scale and PLACS), with satisfactory safety and high tolerability in patients with Alzheimer's Disease (AD). The primary objective will be evaluated using a study endpoint at 1, 13, 26 weeks after initiation of treatment. The secondary objective of this study is to evaluate the benefit of treatment with Nuedexta (20/10) on cognition and functionality as demonstrated in the Rey Auditory Verbal Learning Test (RAVLT), Trail making A and B, Wechsler Memory Scale (WMS) logical memory and delayed recall, Controlled Oral Word Association (COWA), Clinical Dementia Rating (CDR), Neuropsychiatric Inventory (NPI), Alzheimer's Disease Cooperative Study Activities of Daily Living Inventory (ADCSADL) and the 11-item Alzheimer's Disease Assessment Scale-Cognitive subscore (ADAS-Cog11).

Conditions

Alzheimer's Disease; Pseudobulbar Affect (PBA)

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Nuedexta (20/10)

Drug: Nuedexta (20/10) administered orally, two times a day (every 12 hours), during a 26-week period.

Group Type: EXPERIMENTAL

Nuedexta (20/10)

Intervention Type: DRUG

Drug: Nuedexta (20/10) administered orally, two times a day, every 12 hours, during a 26-week period.

Interventions

Nuedexta (20/10)

Drug: Nuedexta (20/10) administered orally, two times a day, every 12 hours, during a 26-week period.

Intervention Type: DRUG

Other Intervention Names

Dextromethorphan/Quinidine

Eligibility Criteria

Inclusion Criteria

• Male/female 55 to 90 years, inclusive.
• Meets National Institute of Neurological and Communicative Disorders and Stroke/Alzheimer's Disease and Related Disorders Association criteria for probable AD.
• Modified Hachinski Ischemia Scale score of ≤4.
• Folstein Mini Mental State Exam score 16-26 at Visit 1.
• Geriatric Depression Scale score ≤6. For patient with history of depression, he/she have been on steady dose of anti-depressant for at least 3 months.
• Clinical history and relevant symptoms of Pseudobulbar Affect.
• Center for Neurologic Study-Lability Scale score at baseline ≥13.
• Stable hematologic, hepatic, and renal function, with no clinically significant symptoms, and with clinical laboratory results (CBC, clinical chemistry, and urinalysis) up to 1-fold higher than upper limit of normal range.
• Resting respiratory rate 12-20/minute.
• MRI or CT scan within past 12 months; no findings inconsistent with diagnosis of AD.
• ECG (within 4 weeks prior to entry)with no evidence of clinically significant abnormalities.
• Concurrent treatment with an acetylcholinesterase inhibitor or memantine allowed; must be on stable dose at least 2 months before screening. Dosing must remain stable throughout the study.
• Use of SSRI's allowed. Must have used for 3 months prior to study entry; dose must remain unchanged during course of study.
• No current symptoms of depressive disorder.
• Score of 19 or lower in the Beck Depression Inventory.
• Agrees to use no prohibited medications during study.

Exclusion Criteria

• Has current serious or unstable illnesses that, in investigator's opinion, could interfere with analysis of safety and efficacy data; has life expectancy <2 years.
• No reliable caregiver in frequent contact with patient (at least 10 hours/week.
• Current or prior history of major psychiatric disturbance.
• Have been in other clinical study within 30 days of entry.
• Score of 20 or higher in Beck Depression Inventory.
• Multiple episodes of head trauma, history within last year of serious infectious disease affecting the brain, head trauma resulting in protracted loss of consciousness, or myasthenia gravis.
• Within the last 5 years, history of a primary or recurrent malignant disease.
• Known sensitivity to quinidine or dextromethorphan.
• History of human immunodeficiency virus, multiple or severe drug allergies, or severe post-treatment hypersensitivity reactions.
• History of chronic alcohol or drug abuse/dependence within the past 5 years.
• Judged by investigator to be at serious risk for suicide.
• Has a recent or current lab result indicating clinically significant lab abnormality.
• At Visit 1 has ALT/SGPT values ≥2 times upper limit of normal (ULN); AST/SGOT values ≥3 times the ULN; total bilirubin values ≥2 times the ULN.
• Resting diurnal oxygen saturation <95%.
• Received dextromethorphan and quinidine within previous 6 months.
• Hypotension (systolic BP <100 mm Hg); postural syncope; unexplained syncope.
• Used medications that affect the CNS (except for AD) for less than 4 weeks.
• On disallowed concomitant medications.
• Experiencing acute exacerbation of underlying neurological disorder within previous 2 months.

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

Sponsors

Avanir Pharmaceuticals

INDUSTRY

Sponsor Role: collaborator

St. Joseph's Hospital and Medical Center, Phoenix

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jiong Shi, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix AZ

Locations

Barrow Neurological Institute

Phoenix, Arizona, United States

Countries

United States

References

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Reference Type: BACKGROUND

PMID: 16387982 (View on PubMed)

Green RL. Regulation of Affect. Semin Clin Neuropsychiatry. 1998 Jul;3(3):195-200.

Reference Type: BACKGROUND

PMID: 10085207 (View on PubMed)

Lieberman A, Benson DF. Control of emotional expression in pseudobulbar palsy. A personal experience. Arch Neurol. 1977 Nov;34(11):717-9. doi: 10.1001/archneur.1977.00500230087017.

Reference Type: BACKGROUND

PMID: 911237 (View on PubMed)

Starkstein SE, Migliorelli R, Teson A, Petracca G, Chemerinsky E, Manes F, Leiguarda R. Prevalence and clinical correlates of pathological affective display in Alzheimer's disease. J Neurol Neurosurg Psychiatry. 1995 Jul;59(1):55-60. doi: 10.1136/jnnp.59.1.55.

Reference Type: BACKGROUND

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Reference Type: BACKGROUND

PMID: 1748077 (View on PubMed)

Pioro EP, Brooks BR, Cummings J, Schiffer R, Thisted RA, Wynn D, Hepner A, Kaye R; Safety, Tolerability, and Efficacy Results Trial of AVP-923 in PBA Investigators. Dextromethorphan plus ultra low-dose quinidine reduces pseudobulbar affect. Ann Neurol. 2010 Nov;68(5):693-702. doi: 10.1002/ana.22093.

Reference Type: BACKGROUND

PMID: 20839238 (View on PubMed)

Strowd RE, Cartwright MS, Okun MS, Haq I, Siddiqui MS. Pseudobulbar affect: prevalence and quality of life impact in movement disorders. J Neurol. 2010 Aug;257(8):1382-7. doi: 10.1007/s00415-010-5550-3. Epub 2010 Apr 8.

Reference Type: BACKGROUND

PMID: 20376475 (View on PubMed)

Wolf JK, Santana HB, Thorpy M. Treatment of "emotional incontinence" with levodopa. Neurology. 1979 Oct;29(10):1435-6. doi: 10.1212/wnl.29.10.1435-b. No abstract available.

Reference Type: BACKGROUND

PMID: 573397 (View on PubMed)

Other Identifiers

AVP923

Identifier Type: -

Identifier Source: org_study_id