CompletedPhase 1ketamine

A Study to Assess the pharmacoMRI Effects of AUT00206 in Healthy Males

Sponsored by Autifony Therapeutics Limited

NCT ID
NCT02935725
Target Enrollment
22 participants
Start Date
2016-10
Est. Completion
2017-11

About This Study

A Phase 1, Single-centre, Double-blind, Placebo controlled Crossover Study to Assess the pharmacoMRI Effects of AUT00206 in Healthy Male Participants

Conditions Studied

Schizophrenia

Interventions

  • Low dose AUT00206 800mg
  • High dose AUT00206 2000 mg
  • Placebo
  • Ketamine
  • Saline

Eligibility

Sex:MALE
Age:18 Years - 45 Years
Healthy Volunteers:Yes
View full eligibility criteria
Inclusion Criteria:

* Male aged 18 to 45 years, inclusive at Visit 1.
* Healthy on the basis of medical history, psychiatric history, physical examination, vital signs, 12-lead electrocardiogram (ECG), haematology, blood chemistry and urinalysis within 6 weeks of Visit 2.
* Right-handed.
* Not a regular smoker (maximum 5 cigarettes per week or equivalent).

Exclusion Criteria:

* History of, or current condition of, migraine headaches or has undergone operations to the head.
* History of significant claustrophobia.

Study Locations (1)

University Of Manchester
London, United Kingdom

This trial is not recruiting

This study has completed enrollment. Check back for results or find similar trials.

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Data Source
ClinicalTrials.gov

Last updated from source