Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Doses of AbGn-168 in Psoriasis

NCT00848055 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2013-11-01

No results posted yet for this study

Summary

The general aim of the trial is to determine the safety, tolerability and pharmacologic profile of single escalating doses of AbGn-168 administered subcutaneously or intravenously to patients with chronic plaque psoriasis

Conditions

Interventions

DRUG

AbGn168 intravenous infusion

single dose intravenous infusion

DRUG

AbGn168 intravenous infusion

single dose intravenous infusion

DRUG

AbGn168 intravenous infusion

single dose intravenous infusion

DRUG

AbGn168 intravenous infusion

single dose intravenous infusion

DRUG

AbGn168 intravenous infusion

single dose intravenous infusion

DRUG

AbGn168 intravenous infusion

single dose intravenous infusion

DRUG

AbGn168 intravenous infusion

single dose intravenous infusion

DRUG

AbGn168 subcutaneous injection

single dose subcutaneous injection

Sponsors & Collaborators

Principal Investigators

  • Boehringer Ingelheim · Boehringer Ingelheim

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2010-10-31

Countries

  • United States
  • Germany

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 NCT00848055 on ClinicalTrials.gov