Safety and Tolerability of AQW051 in Elderly Healthy Volunteers.

NCT00418002 | Completed Phase 1

• 1 other identifier: CAQW051A2102
• Study Type: interventional
• Target: 72
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to assess safety and tolerability of AQW051 administered in single and multiple doses to elderly healthy volunteers. In addition, pharmacokinetic effects will be assessed and the possible effects on cognition.

Conditions

Healthy

Keywords

Single-rising dose , multiple rising dose, elderly, cognitive, , pharmacokinetic, impairment.; Healthy elderly male and female subjects

Outcome Measures

Primary Outcomes (1)

• Safety and tolerability.

Secondary Outcomes (4)

• Pharmacokinetics at the end of the study.

• Effect of AQW051 on cognition as assessed by a computerized cognitive test battery.

• To assess a potential food effect on pharmacokinetics of AQW051.

• To explore the drug abuse liability potential of AQW051.

Interventions

AQW051 DRUG

Eligibility Criteria

• Age: 60 Years - 80 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Healthy male and postmenopausal female subjects between 60 to 80 years of age and in good health as determined by past medical history.
• Male subjects must be using a double-barrier local contraception.
• Body mass index must be within the range of 18 to 33. Subjects must weigh at least 50 kg to participate in this study.
• The regular intake of concomitant drugs including thyroxine, paracetamol, low dose non-steroidal anti-inflammatory drugs, lipid lowering drugs, vitamins and dietary supplements without caffeine and nicotinic acid, and hormone replacement therapy is allowed, if on stable treatment for at least 3 months. Intake of nutritional supplements (e.g. omega-3, vitamins, minerals, cod-liver oil) is allowed.
• Able to communicate well with the investigator, to understand and comply with the requirements of the study. Understand and sign the written informed consent.

You may not qualify if:

• Smokers (use of tobacco products in the previous 3 months).
• Use of any prescription drugs within 4 weeks prior dosing, or over-the-counter medication (e.g. herbal supplements) within 2 weeks prior to study start except noted previously
• Use of any central nervous system active drug and anticholinergic drugs during the previous 3 months and use of any drug or treatment known to cause major organ system toxicity during the previous 3 months is prohibited.
• A past personal or close family medical history of clinically significant cardiac abnormalities.
• Current diagnosis of cardiac arrhythmia derived from ECG and/or Holter ECG.
• Current diagnosis of cardiovascular disease.
• Current diagnosis or history of autonomic dysfunction (e.g. history of fainting, orthostatic hypotension, sinus arrhythmia).
• History of Acute or chronic bronchospastic disease (including asthma and chronic obstructive pulmonary disease) Clinically significant drug allergy or history of atopic allergy (asthma, urticaria, eczematous dermatitis) Known hypersensitivity or severe adverse event to darifenacin or similar drugs Any surgical or medical condition which might significantly alter the absorption, distribution, metabolism or excretion of drugs or which may jeopardize participation in the study Immunodeficiency diseases, including a positive HIV (ELISA and Western blot) test result Positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result. Drug or alcohol abuse within the 12 months prior to dosing.
• Diagnosis of cognitive impairment (Mini Mental State Exam \< 27).
• History or current diagnosis of a cerebrovascular disease (e.g., stroke, transient ischemic attacks, aneurysms).
• Current DSM-IV diagnosis of major depression and/or any other DSM-IV Axis 1 diagnosis that may interfere with the evaluation of the patient's response to study medication, including other primary neurodegenerative dementia, schizophrenia, or bipolar disorder.
• History or current diagnosis of an active, uncontrolled seizure disorder.
• History of head injury or any other neurological disorder.

Sponsors & Collaborators

• Novartis: lead

Study Sites (1)

Novartis Investigative Site

Horsham, United Kingdom

Location

MeSH Terms

Interventions

3-(6-p-tolylpyridin-3-yloxy)-1-azabicyclo(2.2.2)octane

Study Officials

• Novartis

  Investigator site

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY

Study Record Dates

• First Submitted: January 3, 2007
• First Posted: January 4, 2007
• Study Start: May 1, 2006
• Last Updated: June 22, 2007

Record last verified: 2007-06

Locations

GB (1)