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Terminated Phase 2 Interventional

A Trial of NNC0109-0012, an Anti-IL-20 Biologic, in Patients With Active Rheumatoid Arthritis Who Are Inadequate Responders to Methotrexate

ClinicalTrials.gov ID: NCT01636843

Public ClinicalTrials.gov record NCT01636843. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 10, 2026, 11:28 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomised, Double Blind, Placebo-controlled, Multiple Dose, Phase 2b, 24 Week Trial Followed by an Open Label Extension of NNC0109-0012, an Anti-IL-20 Biologic, in Patients With Active Rheumatoid Arthritis Who Are Inadequate Responders to Methotrexate

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial is conducted in Europe, North America and South America. The aim of this trial is to investigate the clinical efficacy of NNC0109-0012, a human monoclonal antibody, compared to placebo when administered as weekly repeat subcutaneous (under the skin) injections in to patients with active rheumatoid arthritis (RA) with inadequate responses to methotrexate (MTX) while on a stable background of MTX therapy.

Study identification

NCT ID
NCT01636843
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
298 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 29, 2012
Primary completion
Nov 9, 2014
Completion
Nov 9, 2014
Last update posted
Sep 4, 2018

2012 – 2014

United States locations

U.S. sites
29
U.S. states
20
U.S. cities
29
Facility City State ZIP Site status
Novo Nordisk Investigational Site Huntington Beach California 92646
Novo Nordisk Investigational Site La Mesa California 91942
Novo Nordisk Investigational Site Los Angeles California 90022
Novo Nordisk Investigational Site Placentia California 92870
Novo Nordisk Investigational Site Upland California 91786
Novo Nordisk Investigational Site Palm Harbor Florida 34684
Novo Nordisk Investigational Site Rock Island Illinois 61201
Novo Nordisk Investigational Site Springfield Illinois 62704
Novo Nordisk Investigational Site South Bend Indiana 46601
Novo Nordisk Investigational Site Cedar Rapids Iowa 52401-2112
Novo Nordisk Investigational Site Wichita Kansas 67206
Novo Nordisk Investigational Site Elizabethtown Kentucky 42701-2988
Novo Nordisk Investigational Site Lake Charles Louisiana 70601
Novo Nordisk Investigational Site Hagerstown Maryland 21740
Novo Nordisk Investigational Site St Louis Missouri 63117
Novo Nordisk Investigational Site Kalispell Montana 59901
Novo Nordisk Investigational Site Freehold New Jersey 07728
Novo Nordisk Investigational Site Toms River New Jersey 08755
Novo Nordisk Investigational Site Albuquerque New Mexico 87102
Novo Nordisk Investigational Site Brooklyn New York 11201-4326
Novo Nordisk Investigational Site Lake Success New York 11042
Novo Nordisk Investigational Site Charlotte North Carolina 28210
Novo Nordisk Investigational Site Norman Oklahoma 73069
Novo Nordisk Investigational Site Orangeburg South Carolina 29118
Novo Nordisk Investigational Site Jackson Tennessee 38305
Novo Nordisk Investigational Site Memphis Tennessee 38119
Novo Nordisk Investigational Site Houston Texas 77008
Novo Nordisk Investigational Site Mesquite Texas 75150-5615
Novo Nordisk Investigational Site Beckley West Virginia 25801-2805

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 110 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01636843, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 4, 2018 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01636843 live on ClinicalTrials.gov.

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