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Terminated Phase 2 Interventional Results available

Efficacy and Safety of TD-1473 in Crohn's Disease

ClinicalTrials.gov ID: NCT03635112

Public ClinicalTrials.gov record NCT03635112. 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 Oct 19, 2026, 1:09 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 2 Multi-Center, Randomized, Double-Blind, Placebo˗Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Induction Therapy With 2 Doses of TD-1473 in Subjects With Moderately-to-Severely Active Crohn's Disease

Brief summary

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

A Phase 2 study to evaluate the efficacy, safety and tolerability of TD-1473 in subjects with moderately-to-severely active Crohn's Disease with up to 48 weeks of treatment.

Study identification

NCT ID
NCT03635112
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Theravance Biopharma
Industry
Enrollment
167 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Nov 19, 2018 (Actual)
Primary completion
Dec 30, 2021 (Actual)
Completion
Dec 30, 2021 (Actual)
Last update posted
Mar 13, 2023

2018 – 2021

United States locations

U.S. sites
44
U.S. states
19
U.S. cities
42
Facility City State ZIP Site status
Theravance Biopharma Investigational Site Birmingham Alabama 35233-2110 —
Theravance Biopharma Investigational Site Mobile Alabama 36688 —
Theravance Biopharma Investigational Site Scottsdale Arizona 85259-5499 —
Theravance Biopharma Investigational Site La Jolla California 92093 —
Theravance Biopharma Investigational Site Los Angeles California 90048 —
Theravance Biopharma Investigational Site Oakland California 94612 —
Theravance Biopharma Investigational Site Santa Monica California 90404 —
Theravance Biopharma Investigational Site Aventura Florida 33180 —
Theravance Biopharma Investigational Site Clearwater Florida 33765 —
Theravance Biopharma Investigational Site Hialeah Florida 33013 —
Theravance Biopharma Investigational Site Hollywood Florida 33021 —
Theravance Biopharma Investigational Site Largo Florida 33777 —
Theravance Biopharma Investigational Site Miami Florida 33135 —
Theravance Biopharma Investigational Site New Port Richey Florida 34653 —
Theravance Biopharma Investigational Site St. Petersburg Florida 33710 —
Theravance Biopharma Investigational Site Tampa Florida 33603 —
Theravance Biopharma Investigational Site Tampa Florida 33606 —
Theravance Biopharma Investigational Site New Lenox Illinois 60451 —
Theravance Biopharma Investigational Site Kansas City Kansas 66160 —
Theravance Biopharma Investigational Site Louisville Kentucky 40202 —
Theravance Biopharma Investigational Site Rockville Maryland 20850 —
Theravance Biopharma Investigational Site Brockton Massachusetts 02302 —
Theravance Biopharma Investigational Site Wyoming Michigan 49519 —
Theravance Biopharma Investigational Site St Louis Missouri 63110 —
Theravance Biopharma Investigational Site Las Vegas Nevada 89133 —
Theravance Biopharma Investigational Site Utica New York 13502 —
Theravance Biopharma Investigational Site Gastonia North Carolina 28504 —
Theravance Biopharma Investigational Site Greenville North Carolina 27834 —
PMG Research of Salisbury Salisbury North Carolina 28144 —
Theravance Biopharma Investigational Site Tulsa Oklahoma 74136 —
Theravance Biopharma Investigational Site Pittsburgh Pennsylvania 15212 —
Theravance Biopharma Investigational Site Uniontown Pennsylvania 15401 —
Theravance Biopharma Investigational Site Orangeburg South Carolina 29118 —
Theravance Biopharma Investigational Site Rock Hill South Carolina 29732 —
Theravance Biopharma Investigational Site Boerne Texas 78006 —
Theravance Biopharma Investigational Site El Paso Texas 79936 —
Theravance Biopharma Investigational Site Garland Texas 75044 —
Theravance Biopharma Investigational Site Harlingen Texas 78550 —
Theravance Biopharma Investigational Site Houston Texas 77058 —
Theravance Biopharma Investigational Site San Antonio Texas 78215 —
Theravance Biopharma Investigational Site San Antonio Texas 78229 —
Theravance Biopharma Investigational Site Southlake Texas 76092 —
Theravance Biopharma Investigational Site Spring Texas 77386 —
Theravance Biopharma Investigational Site Lansdowne Town Center Virginia 20176 —

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 134 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03635112, 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 Mar 13, 2023 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03635112 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →