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

NCT01301456 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 84

Last updated 2018-02-09

Study results available
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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

BIOLOGICAL

Placebo

Single subcutaneous injection of placebo

BIOLOGICAL

PF-04856883

Single subcutaneous injection of PF-04856883

BIOLOGICAL

PF-04856883

Single subcutaneous injection of PF-04856883

BIOLOGICAL

PF-04856883

Single subcutaneous injection of PF-04856883

BIOLOGICAL

Placebo

Single subcutaneous injection of placebo

BIOLOGICAL

PF-04856883

Single subcutaneous injection of PF-04856883

BIOLOGICAL

PF-04856883

Single subcutaneous injection of PF-04856883

BIOLOGICAL

PF-04856883

Single subcutaneous injection of PF-04856883

BIOLOGICAL

Placebo

Multiple weekly subcutaneous injections of placebo for 3 weeks

BIOLOGICAL

PF-04856883

Multiple weekly subcutaneous injections of PF-04856883 for 3 weeks

BIOLOGICAL

PF-04856883

Multiple weekly subcutaneous injections of PF-04856883 for 3 weeks

BIOLOGICAL

PF-04856883

Multiple weekly subcutaneous injections of PF-04856883 for 3 weeks

BIOLOGICAL

PF-04856883

Multiple weekly subcutaneous injections of PF-04856883 for 3 weeks

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2011-12-31
Completion
2012-04-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01301456 on ClinicalTrials.gov