A Phase 1 Study To Evaluate The Safety And Tolerability Of PF-06252616 In Healthy Subjects

NCT01616277 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 86

Last updated 2014-09-25

No results posted yet for this study

Summary

The purpose of this study is to determine if the study drug, PF-06252616 is safe and well tolerated when given to adult healthy volunteers.

Conditions

  • Healthy

Interventions

BIOLOGICAL

PF-06252616

1.0 milligram per kilogram of PF-06252616, IV infusion, single dose

DRUG

Placebo

Placebo for PF-06252616, IV infusion, single dose

BIOLOGICAL

PF-06252616

3.0 milligram per kilogram of PF-06252616, IV infusion, single dose

DRUG

Placebo

Placebo for PF-06252616, IV infusion, single dose

BIOLOGICAL

PF-06252161

10.0 milligram per kilogram of PF-06252616, IV infusion, single dose

DRUG

Placebo

Placebo for PF-06252616, IV infusion, single dose

BIOLOGICAL

PF-06252616

3.0 milligram per kilogram of PF-06252616, Subcutaneous injection, single dose

DRUG

Placebo

Placebo for PF-06252616, Subcutaneous injection, single dose

BIOLOGICAL

PF-06252616

10.0 miligram per kilogram of PF-06252616, IV infusion, repeat dose

DRUG

Placebo

Placebo for PF-06252616, IV infusion, repeat dose

BIOLOGICAL

PF-06252616

20.0 milligram per kilogram of PF-06252616, IV infusion, single dose

DRUG

Placebo

Placebo for PF-06252616, IV infusion, single dose

BIOLOGICAL

PF-06252616

40.0 milligram per kilogram of PF-06252616, IV infusion, single dose

DRUG

Placebo

Placebo for PF-06252616, IV infusion, single dose

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
64 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2014-08-31
Completion
2014-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs
Companies

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 NCT01616277 on ClinicalTrials.gov