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Study to Investigate Safety, Tolerability and Pharmacokinetics of a Single Ascending Dose of AZD1704

AstraZeneca logo

AstraZeneca

Status and phase

Completed
Phase 1

Conditions

Pain

Treatments

Drug: AZD1704

Study type

Interventional

Funder types

Industry

Identifiers

NCT00692042
D0980C00001

Details and patient eligibility

About

The primary aim for this study is to investigate the safety and tolerability of the AZD1704, first time in man.

Enrollment

80 patients

Sex

All

Ages

20 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteers, man or woman of non child-bearing potential
  • Provision of signed informed consent.

Exclusion criteria

  • History of somatic disease/condition that may interfere with the objectives ot the study, as judged by the Investigator. History of seizures, with the exception of single occasions fever induced seizures in childhood.
  • History of previous or ongoing psychiatric disease/condition including psychosis, affective disorder, anxiety disorder, borderline state and personality disorder according to the criteria in the DSM of Mental Disorder, 4th edition
  • History of use of antipsychotic, antidepressant or anxiolytic drugs for the treatment of psychiatric disease or symptoms, prescribed as well as non-prescribed use.

Trial design

80 participants in 1 patient group

1
Experimental group
Treatment:
Drug: AZD1704

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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