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Brain Imaging Study of F17464

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01689038
Enrollment
8
Registered
2012-09-20
Start date
2012-11-30
Completion date
2013-02-28
Last updated
2013-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Volunteers

Brief summary

Assess the binding rate of F17464 to cerebral receptors in healthy volunteers.

Interventions

DRUGF17464

Single dose

Sponsors

Pierre Fabre Medicament
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Male healthy volunteers

Exclusion criteria

* Presence or positive history of severe medical illness or psychiatric conditions

Design outcomes

Primary

MeasureTime frameDescription
Binding rate to cerebral receptorsup to 29 hoursby brain imaging

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026