A Study of AK106-001616 in Patients With Rheumatoid Arthritis (RA)

NCT01285752 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 240

Last updated 2016-07-25

No results posted yet for this study

Summary

To investigate the efficacy and safety of AK106-001616 in patients with rheumatoid arthritis.

Conditions

Interventions

DRUG

AK106-001616

DRUG

AK106-001616

DRUG

Active comparator

Sponsors & Collaborators

  • Asahi Kasei Pharma Corporation

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2011-02-28
Primary Completion
2012-01-31
Completion
2012-12-31

Countries

  • Czechia
  • Germany
  • Hungary
  • Poland
  • Slovakia
  • Ukraine
  • United Kingdom

Study Locations

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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 NCT01285752 on ClinicalTrials.gov