Double Blind Study of Trp01 in Patients With Alzheimer's Disease

Alzheimer's Disease Clinical Trial

Official title:

Double Blind Medium Term Efficacy Study of Trp01 in Patients With Mild to Moderate Alzheimer's Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00202124
• Other study ID #: DFW-TRP01
• Status: Completed
• Phase: Phase 4
• First received: September 13, 2005
• Last updated: September 13, 2005
• Start date: April 2001
• Est. completion date: March 2002

Study information

• Verified date: November 2002
• Source: Queen's University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Health Canada
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine whether tryptophan is effective in the treatment of mild to moderate Alzheimer's Disease (AD).

Description:

The clinical trial will be a double-blind, placebo-controlled study with patients being randomized in a 2:1 ratio into groups A and B, respectively:

Group A: TRP01 1g b.i.d. for 26 weeks

Group B: placebo capsules b.i.d. for 26 weeks

After the initial screening, clinic visits will take place at 0, 13 and 26 weeks. The blinding will be maintained until all patients have completed the 26-week trial. Any patients wishing to continue taking the medication upon completion of the trial will be provided a prescription for the drug and may purchase it at their own expense.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 12
• Est. completion date: March 2002
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A and older

Eligibility

Inclusion Criteria:

Patients will be selected in order to fulfill both of the following definitions:

• Dementia according to DSM-IV criteria :

• development of multiple cognitive deficits manifested by both memory impairment and one or more of the following cognitive disturbances: aphasia, apraxia, agnosia, disturbance in executive functioning

• the above-mentioned deficits cause significant impairment in social or occupational functioning

• they do not occur exclusively during the course of delirium

• Dementia according to communicative disorders and stroke criteria (NINCDS-ADRDA)

• dementia established clinically and documented by a Folstein Mini-Mental State Examination (MMSE)

• deficits in two or more areas of cognition

• progressive worsening of memory and other cognitive functions

• no disturbance of consciousness

• absence of systematic disorders or other brain diseases that in and of themselves can account for progressive deficit in memory and cognition

Furthermore, patients must fulfill the following criteria:

• men, or postmenopausal or surgically sterilized women

• with severity of dementia of mild to moderate degree as reflected by a score of greater than 14 but less than 26 on the MMSE

• with a minimum one-year duration of the symptomatology (progressive worsening of memory and other cognitive functions)

• living at home or in an institution provided that they have reliable caregivers

• able to perform the required psychometric tests and evaluations. Visual and auditory acuity (with glasses or hearing aid if required) must be sufficient to complete the protocol-specified procedures.

• Clinical laboratory battery (see section 7.2.2) must yield results within normal limits or determined as not clinically significant by the study physician for the patient’s sex and age

• Patients and their substitute decision-makers must have signed the written informed consent form

Exclusion Criteria:

Patients with any of the following will not be included in the study:

• Patients with any other cause of dementia as evidenced by medical history, general physical and neurological examination, laboratory tests, and neuroradiological findings:

• Vascular dementia, as evidenced by Modified Hachinski Ischemia Scale

• Depressive pseudementia, as evidenced by cognitive disturbances concomitant to a major depressive episode according to DSM-IV and/or a history of more than one major depressive episode

• DSM-IV criteria for any major psychiatric disorder including schizophrenia, alcohol or substance abuse

• Huntington’s chorea or Parkinson’s disease, evidenced by neurological examination, with an onset prior to or concurrent with dementia

• Creutzfeldt-Jakob disease

• Intracranial mass lesion

• Clinically important head injury

• History or current evidence of stroke

• Onset of dementia following cardiac arrest or heart surgery

• Neurosyphilis

• Seropositivity for HIV

• Vitamin B12 deficiency

• Uncorrected hypothyroidism (i.e. abnormal free T4, ultrasensitive TSH)

• Patients with other relevant concomitant diseases:

• Patients with history or current evidence of a sleep disorder

• Patients with a clinically significant cardiovascular, renal, hepatic, pulmonary, gastrointestinal, endocrine, metabolic, opthalmologic, or hematologic condition

• Current evidence or history within the past year of myocardial infarction (MI), congestive heart failure

• Blood pressure at screening of > 180 mm Hg systolic or 100 mm Hg diastolic

• Impaired renal, hepatic, or gastrointestinal function, which could interfere with drug absorption, metabolism or excretion

• Seizure disorder

• Diabetes

• Earlier diagnosis or current evidence of cataracts

• Progressive fatal disease (other than AD)

• Treatment with any other investigational drug in the last 8 weeks prior to screening

• Previous administration of TRP01

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Alzheimer Disease
• Alzheimer's Disease

Intervention

Drug:
• Tryptophan

Locations

Country	Name	City	State
Canada	Queen's University	Kingston	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
Queen's University

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	1. MMSE score
Primary	2. Alzheimer’s Disease Assessment Scale, cognitive subpart (ADAS-Cog) as an evaluation of cognitive functioning
Secondary	1. Alzheimer’s Disease Cooperative Study – Clinical Global Impression of Change (ADCS-CGIC)
Secondary	2. Neuropsychiatric Inventory (NPI)
Secondary	3. Disability Assessment for Dementia (DAD)
Secondary	4. Physical Self-Maintenance Scale (PSMS)
Secondary	5. Functional Activities Questionnaire (FAQ)