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Completed Phase 2 Interventional Results available

Evaluation of Efficacy and Safety of MEDI2070 in Patients With Active, Moderate-to-severe Crohn's Disease.

ClinicalTrials.gov ID: NCT01714726

Public ClinicalTrials.gov record NCT01714726. 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 11, 2026, 5:29 PM 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 Phase 2a Study to Evaluate the Efficacy and Safety of MEDI2070 in Subjects With Moderate to Severe Crohn's Disease Who Have Failed or Are Intolerant to Anti-tumor Necrosis Factor-alpha Therapy

Brief summary

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

The study is designed to evaluate the clinical efficacy and safety of MEDI2070 as compared to placebo. Investigational product will be administered as intravenous infusion in double-blind period, and as a subcutaneous injection in open-label period

Study identification

NCT ID
NCT01714726
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
121 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 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
Jan 31, 2013
Primary completion
May 19, 2014
Completion
Dec 13, 2016
Last update posted
May 25, 2021

2013 – 2016

United States locations

U.S. sites
26
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
Research Site Encinitas California 92024
Research Site Los Angeles California 45242
Research Site San Diego California 92114
Research Site Torrance California 90505
Research Site Lakewood Colorado 80215
Research Site Jacksonville Florida 32256
Research Site Miami Florida 33136
Research Site Winter Park Florida 32789
Research Site Macon Georgia 31201
Research Site Chicago Illinois 60637
Research Site Baton Rouge Louisiana 70809
Research Site Hammond Louisiana 70403
Research Site Baltimore Maryland 21201
Research Site Chevy Chase Maryland 20815
Research Site Ann Arbor Michigan 48109
Research Site Troy Michigan 48098
Research Site Belton Missouri 64012
Research Site New York New York 10021
Research Site New York New York 10029
Research Site Asheville North Carolina 28801
Research Site Charlotte North Carolina 28207
Research Site Cincinnati Ohio 45219
Research Site Lima Ohio 45806
Research Site Germantown Tennessee 38138
Research Site San Antonio Texas 78229
Research Site Seattle Washington 98195

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 54 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01714726, 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 May 25, 2021 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01714726 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →