Last updated: 11/03/2018 12:26:57
An open label positron emission tomography study in healthy male subjects to compare binding of the D2/3 agonist radiotracer 11CPHNO with that of reference D2/3 antagonist 11Craclopride, in terms of vulnerability to changes in endogenous dopamine elicited by an acute amphetamine challenge
Clinicaltrials.gov ID
Not applicable
EudraCT ID
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EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: An open label positron emission tomography study in healthy male subjects to compare binding of the D2/3 agonist radiotracer 11CPHNO with that of reference D2/3 antagonist 11Craclopride, in terms of vulnerability to changes in endogenous dopamine elicited by an acute amphetamine challenge
Trial description: An open label positron emission tomography study in healthy male subjects to compare binding of the D2/3 agonist radiotracer 11CPHNO with that of reference D2/3 antagonist 11Craclopride, in terms of vulnerability to changes in endogenous dopamine elicited by an acute amphetamine challenge
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2010-17-02
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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