A Study of Adalimumab After Dose Escalation in Japanese Subjects With Crohn's Disease

NCT01958827 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2016-04-12

Study results available
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Summary

The purpose of this study is to investigate the efficacy, safety and pharmacokinetics after dose escalation in Japanese subjects with Crohn's Disease.

Conditions

Interventions

BIOLOGICAL

Adalimumab

Adalimumab pre-filled syringe, administered by subcutaneous injection.

Sponsors & Collaborators

Principal Investigators

  • Morio Ozawa, MS · AbbVie

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2015-03-31
Completion
2015-10-31

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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 NCT01958827 on ClinicalTrials.gov