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Study Evaluating the Effect of Lecozotan SR on the QTc Interval

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Wyeth

Status and phase

Completed
Phase 1

Conditions

Healthy
Alzheimer Disease

Treatments

Drug: Moxifloxacin
Drug: Lecozotan SR

Study type

Interventional

Funder types

Industry

Identifiers

NCT00499642
3098B1-133

Details and patient eligibility

About

This is a randomized, double-blind, placebo- and moxifloxacin (open-label)-controlled, 4-period crossover study.

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women and men aged 18 to 55 years inclusive.
  • Healthy as determined by the investigator on the basis of medical history, physical examination, clinical laboratory test results, vital signs, and 12-lead electrocardiogram (ECG).

Exclusion criteria

  • History of any clinically important drug allergy.
  • Positive findings of urine drug screen (eg, amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine, and opiates).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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