Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Repeated Doses of PF-04958242 in Healthy Volunteers
Completed · Phase 1 · Has a placebo group
Conditions studied: Schizophrenia
In brief
This study aims to assess the safety, tolerability, and pharmacokinetics of PF-04958242 at a number of ascending doses administered once daily for 14 days in healthy volunteers.
Key facts
- Study ID
- NCT01511510
- Run by
- Biogen
- People needed
- 39
- Starts
- 2011-06-01
- Expected to finish
- 2011-11-01
- Last updated by the study team
- 2019-11-21
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy male and/or female subjects of non-child bearing potential Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight >50 kg (110 lbs)
You may not qualify if…
- Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease
- History of seizures or of a condition with risk of seizures
- Pregnant or nursing females, and females of child bearing potential
Where it is running
- Pfizer Investigational Site — New Haven, Connecticut, United States
Full record on ClinicalTrials.gov
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