A Phase 1 Study To Evaluate The Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Of Pf-05230907 In Healthy Volunteers

NCT01897142 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 49

Last updated 2016-04-22

No results posted yet for this study

Summary

The purpose of this study is to determine what the study drug does to the body, what the body does to the study drug, and if the study drug is safe and well tolerated when given to adult healthy volunteers.

Conditions

  • Healthy

Interventions

BIOLOGICAL

PF-05230907

0.1 micrograms per kilogram of PF-05230907, IV bolus, single dose

DRUG

Placebo for PF-05230907

0.1 micrograms per kilogram of placebo for PF-05230907, IV bolus, single dose

BIOLOGICAL

PF-05230907

0.3 micrograms per kilogram of PF-05230907, IV bolus, single dose

DRUG

Placebo for PF-05230907

0.3 micrograms per kilogram of placebo for PF-05230907, IV bolus, single dose

BIOLOGICAL

PF-05230907

1 micrograms per kilogram of PF-05230907, IV bolus, single dose

DRUG

Placebo for PF-05230907

1 micrograms per kilogram of placebo for PF-05230907, IV bolus, single dose

BIOLOGICAL

PF-05230907

2 micrograms per kilogram of PF-05230907, IV bolus, single dose

DRUG

Placebo for PF-05230907

2 micrograms per kilogram of placebo for PF-05230907, IV bolus, single dose

BIOLOGICAL

PF-05230907

3 micrograms per kilogram of PF-05230907, IV bolus, single dose

DRUG

Placebo for PF-05230907

3 micrograms per kilogram of placebo for PF-05230907, IV bolus, single dose

BIOLOGICAL

PF-05230907

5 micrograms per kilogram of PF-05230907, IV bolus, single dose

DRUG

Placebo for PF-05230907

5 micrograms per kilogram of placebo for PF-05230907, IV bolus, single dose

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE

Eligibility

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

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2015-03-31
Completion
2015-03-31

Countries

  • Belgium

Study Locations

More Related Trials

Entities

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 NCT01897142 on ClinicalTrials.gov