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Clinical Trials/NCT00331175
NCT00331175
Completed
Phase 1

A Phase 1, Randomized, Placebo- And Positive Controlled Study To Assess The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of Single Escalating Doses Of Intravenous Peptide YY3-36 In Otherwise Healthy Overweight Adult Subjects

Pfizer1 site in 1 country31 target enrollmentJuly 2006
ConditionsObesity

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Obesity
Sponsor
Pfizer
Enrollment
31
Locations
1
Primary Endpoint
Food intake
Status
Completed
Last Updated
19 years ago

Overview

Brief Summary

The purpose of this trial is to evaluate the safety and tolerability of single escalating doses of Peptide YY3-36 and to determine effects on food intake and serum hormones when administered by intravenous infusion to otherwise healthy overweight adult subjects.

Registry
clinicaltrials.gov
Start Date
July 2006
End Date
December 2006
Last Updated
19 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Pfizer

Eligibility Criteria

Inclusion Criteria

  • BMI 27-35 kg/m2

Exclusion Criteria

  • Women of childbearing potential

Outcomes

Primary Outcomes

Food intake

Secondary Outcomes

  • Plasma biomarkers, safety, toleration

Study Sites (1)

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