Clinical Trials Directory

Trials / Completed

CompletedNCT01301456

Single-Dose And Multiple-Dose Safety And Tolerability Study Of PF-04856883 In Type 2 Diabetic Adult Females

A Phase 1, Double-blind, Placebo-controlled, Randomized, Parallel Group Study To Assess The Safety, Tolerability, Pharmacokinetics, And Pharmacodynamics Of Pf-04856883 In Adult Female Subjects With Type 2 Diabetes Mellitus

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
84 (actual)
Sponsor
Pfizer · Industry
Sex
Female
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this study is to evaluate the safety and tolerability of PF-04856883 (CVX-096) in adult female subjects with Type 2 diabetes mellitus on high dose of metformin.

Conditions

Interventions

TypeNameDescription
BIOLOGICALPlaceboSingle subcutaneous injection of placebo
BIOLOGICALPF-04856883Single subcutaneous injection of PF-04856883
BIOLOGICALPF-04856883Single subcutaneous injection of PF-04856883
BIOLOGICALPF-04856883Single subcutaneous injection of PF-04856883
BIOLOGICALPlaceboSingle subcutaneous injection of placebo
BIOLOGICALPF-04856883Single subcutaneous injection of PF-04856883
BIOLOGICALPF-04856883Single subcutaneous injection of PF-04856883
BIOLOGICALPF-04856883Single subcutaneous injection of PF-04856883
BIOLOGICALPlaceboMultiple weekly subcutaneous injections of placebo for 3 weeks
BIOLOGICALPF-04856883Multiple weekly subcutaneous injections of PF-04856883 for 3 weeks
BIOLOGICALPF-04856883Multiple weekly subcutaneous injections of PF-04856883 for 3 weeks
BIOLOGICALPF-04856883Multiple weekly subcutaneous injections of PF-04856883 for 3 weeks
BIOLOGICALPF-04856883Multiple weekly subcutaneous injections of PF-04856883 for 3 weeks

Timeline

Start date
2011-03-01
Primary completion
2011-12-01
Completion
2012-04-01
First posted
2011-02-23
Last updated
2018-02-09
Results posted
2018-02-09

Locations

7 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01301456. Inclusion in this directory is not an endorsement.