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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 Anti-TNFa Biologics

ClinicalTrials.gov ID: NCT01636817

Public ClinicalTrials.gov record NCT01636817. 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 Nov 6, 2026, 8:40 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. 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 Anti-TNFa Biologics

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 s.c. (subcutaneous, under the skin) injections to patients with active rheumatoid arthritis (RA) who are inadequate responders to anti-TNFa biologics and are on a stable background of methotrexate (MTX) therapy.

Study identification

NCT ID
NCT01636817
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
239 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
Aug 2012 (Type not available)
Primary completion
Nov 2014 (Actual)
Completion
Nov 2014 (Actual)
Last update posted
Sep 5, 2018

2012 – 2014

United States locations

U.S. sites
92
U.S. states
32
U.S. cities
84
Facility City State ZIP Site status
Novo Nordisk Investigational Site Huntsville Alabama 35801 —
Novo Nordisk Investigational Site Tuscaloosa Alabama 35406 —
Novo Nordisk Investigational Site Mesa Arizona 85202 —
Novo Nordisk Investigational Site Phoenix Arizona 85037 —
Novo Nordisk Investigational Site Scottsdale Arizona 85258-4523 —
Novo Nordisk Investigational Site Glendale California 91204 —
Novo Nordisk Investigational Site Hemet California 92543 —
Novo Nordisk Investigational Site Huntington Beach California 92646 —
Novo Nordisk Investigational Site La Mesa California 91942 —
Novo Nordisk Investigational Site Lakewood California 90712 —
Novo Nordisk Investigational Site Long Beach California 90806 —
Novo Nordisk Investigational Site Long Beach California 90808-2146 —
Novo Nordisk Investigational Site Los Angeles California 90022 —
Novo Nordisk Investigational Site Placentia California 92870 —
Novo Nordisk Investigational Site San Diego California 92101 —
Novo Nordisk Investigational Site Santa Monica California 90409 —
Novo Nordisk Investigational Site Upland California 91786 —
Novo Nordisk Investigational Site Boca Raton Florida 33486 —
Novo Nordisk Investigational Site Fort Lauderdale Florida 33334 —
Novo Nordisk Investigational Site Gainesville Florida 32607 —
Novo Nordisk Investigational Site Jupiter Florida 33468 —
Novo Nordisk Investigational Site New Port Richey Florida 34652 —
Novo Nordisk Investigational Site Ocala Florida 34474 —
Novo Nordisk Investigational Site Orlando Florida 32804 —
Novo Nordisk Investigational Site Tampa Florida 33613 —
Novo Nordisk Investigational Site Venice Florida 34292 —
Novo Nordisk Investigational Site West Palm Beach Florida 33407 —
Novo Nordisk Investigational Site Decatur Georgia 30033 —
Novo Nordisk Investigational Site Idaho Falls Idaho 83404 —
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 Kansas City Kansas 66160 —
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 Shreveport Louisiana 71105 —
Novo Nordisk Investigational Site Baltimore Maryland 21239 —
Novo Nordisk Investigational Site Columbia Maryland 21045 —
Novo Nordisk Investigational Site Cumberland Maryland 21502 —
Novo Nordisk Investigational Site Hagerstown Maryland 21740 —
Novo Nordisk Investigational Site Worcester Massachusetts 01605 —
Novo Nordisk Investigational Site Ann Arbor Michigan 48109-0100 —
Novo Nordisk Investigational Site Battle Creek Michigan 49018 —
Novo Nordisk Investigational Site Flowood Mississippi 39232-9306 —
Novo Nordisk Investigational Site Flowood Mississippi 39232 —
Novo Nordisk Investigational Site St Louis Missouri 63117 —
Novo Nordisk Investigational Site St Louis Missouri 63139-2338 —
Novo Nordisk Investigational Site St Louis Missouri 63141-6819 —
Novo Nordisk Investigational Site Lincoln Nebraska 68516 —
Novo Nordisk Investigational Site Clifton New Jersey 07012 —
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 Albany New York 12206 —
Novo Nordisk Investigational Site Brooklyn New York 11201-4326 —
Novo Nordisk Investigational Site Lake Success New York 11042 —
Novo Nordisk Investigational Site Chapel Hill North Carolina 27599 —
Novo Nordisk Investigational Site Charlotte North Carolina 28210 —
Novo Nordisk Investigational Site Greensboro North Carolina 27408 —
Novo Nordisk Investigational Site Raleigh North Carolina 27617 —
Novo Nordisk Investigational Site Wilmington North Carolina 28401-6442 —
Novo Nordisk Investigational Site Cincinnati Ohio 45219 —
Novo Nordisk Investigational Site Columbus Ohio 43203 —
Novo Nordisk Investigational Site Toledo Ohio 43606 —
Novo Nordisk Investigational Site Norman Oklahoma 73069 —
Novo Nordisk Investigational Site Oklahoma City Oklahoma 73103 —
Novo Nordisk Investigational Site Tulsa Oklahoma 74135 —
Novo Nordisk Investigational Site Bend Oregon 97701 —
Novo Nordisk Investigational Site Lake Oswego Oregon 07035 —
Novo Nordisk Investigational Site Hershey Pennsylvania 17033-2360 —
Novo Nordisk Investigational Site Charleston South Carolina 29406 —
Novo Nordisk Investigational Site Charleston South Carolina 29407-7757 —
Novo Nordisk Investigational Site Columbia South Carolina 29204-2409 —
Novo Nordisk Investigational Site Orangeburg South Carolina 29118 —
Novo Nordisk Investigational Site Jackson Tennessee 38305 —
Novo Nordisk Investigational Site Memphis Tennessee 38104 —
Novo Nordisk Investigational Site Memphis Tennessee 38119 —
Novo Nordisk Investigational Site Amarillo Texas 79124 —
Novo Nordisk Investigational Site Austin Texas 78721 —
Novo Nordisk Investigational Site Carrollton Texas 75007 —
Novo Nordisk Investigational Site Houston Texas 77008 —
Novo Nordisk Investigational Site Houston Texas 77034 —
Novo Nordisk Investigational Site Houston Texas 77090 —
Novo Nordisk Investigational Site McKinney Texas 75071 —
Novo Nordisk Investigational Site Sugar Land Texas 77479 —
Novo Nordisk Investigational Site Waco Texas 76708-3244 —
Novo Nordisk Investigational Site Arlington Virginia 22205 —
Novo Nordisk Investigational Site Seattle Washington 98122 —
Novo Nordisk Investigational Site Tacoma Washington 98405 —
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 72 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01636817, 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 5, 2018 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01636817 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →