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Terminated Phase 2 Interventional Results available

A Study to Test if TEV-53275 is Effective in Relieving Asthma

ClinicalTrials.gov ID: NCT04847674

Public ClinicalTrials.gov record NCT04847674. 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 28, 2026, 11:45 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 Phase 2, Multicenter, Randomized, Double Blind, Placebo Controlled, Parallel Group Study to Assess the Safety, Efficacy and Pharmacodynamics of TEV 53275 Administered Subcutaneously in Adult Patients With Persistent Eosinophilic Asthma

Brief summary

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

The primary objective of the study is to evaluate the efficacy of TEV-53275 administered subcutaneously (sc) in adult participants with persistent asthma and an eosinophilic phenotype compared to placebo. A secondary objective is to evaluate the efficacy of TEV-53275 compared to placebo assessed by lung function, asthma symptoms, rescue medication use, and quality of life measures. Another secondary objective is to evaluate the safety and tolerability of TEV-53275 administered sc in adult participants with persistent asthma and an eosinophilic phenotype compared with placebo, and lastly, to evaluate the immunogenicity of TEV-53275 administered sc in adult participants with persistent asthma and an eosinophilic phenotype.

Study identification

NCT ID
NCT04847674
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
97 participants

Conditions and interventions

Conditions

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
May 3, 2021
Primary completion
Apr 27, 2022
Completion
Apr 27, 2022
Last update posted
Jun 7, 2023

2021 – 2022

United States locations

U.S. sites
77
U.S. states
25
U.S. cities
65
Facility City State ZIP Site status
Teva Investigational Site 15188 Hoover Alabama 35244 —
Teva Investigational Site 15174 Peoria Arizona 85381 —
Teva Investigational Site 15202 Phoenix Arizona 85031 —
Teva Investigational Site 15205 Tucson Arizona 85712 —
Teva Investigational Site 15178 Bakersfield California 93301 —
Teva Investigational Site 15196 Bakersfield California 93309 —
Teva Investigational Site 15176 Encinitas California 92024 —
Teva Investigational Site 15156 Huntington Beach California 92647 6818 —
Teva Investigational Site 15209 Inglewood California 90303 —
Teva Investigational Site 15194 Los Angeles California 90017 —
Teva Investigational Site 15143 Los Angeles California 90025 —
Teva Investigational Site 15212 Los Angeles California 91436 —
Teva Investigational Site 15151 Mission Viejo California 92691 —
Teva Investigational Site 15210 North Hollywood California 91606 —
Teva Investigational Site 15136 San Jose California 95117 —
Teva Investigational Site 15157 Stockton California 95207 —
Teva Investigational Site 15158 Upland California 91786 —
Teva Investigational Site 15167 Walnut Creek California 94598 —
Teva Investigational Site 15133 Westminster California 92683 —
Teva Investigational Site 15166 Colorado Springs Colorado 80907 —
Teva Investigational Site 15200 Lafayette Colorado 80026 —
Teva Investigational Site 15139 Wheat Ridge Colorado 80033 —
Teva Investigational Site 15182 Boynton Beach Florida 33435 —
Teva Investigational Site 15147 Hialeah Florida 33012 —
Teva Investigational Site 15134 Hialeah Florida 33016 —
Teva Investigational Site 15152 Leesburg Florida 34748 —
Teva Investigational Site 15149 Miami Florida 33144 —
Teva Investigational Site 15211 Miami Florida 33155 —
Teva Investigational Site 15206 Miami Florida 33165 —
Teva Investigational Site 15215 Miami Florida 33165 —
Teva Investigational Site 15141 Miami Florida 33173 —
Teva Investigational Site 15169 Miami Lakes Florida 33014 —
Teva Investigational Site 15170 North Palm Beach Florida 33408 —
Teva Investigational Site 15130 Orlando Florida 32819 —
Teva Investigational Site 15140 Tallahassee Florida 32308-4355 —
Teva Investigational Site 15132 Tampa Florida 33607 —
Teva Investigational Site 15135 Sugar Hill Georgia 30518 —
Teva Investigational Site 15183 Normal Illinois 61761 —
Teva Investigational Site 15198 Overland Park Kansas 66210 —
Teva Investigational Site 15187 Zachary Louisiana 70791 —
Teva Investigational Site 15148 Baltimore Maryland 21236 —
Teva Investigational Site 15190 North Dartmouth Massachusetts 02747 —
Teva Investigational Site 15175 Columbia Missouri 65203 —
Teva Investigational Site 15145 Rolla Missouri 65401 —
Teva Investigational Site 15144 St Louis Missouri 63141 —
Teva Investigational Site 15137 Bellevue Nebraska 68123-4303 —
Teva Investigational Site 15164 Skillman New Jersey 08558 —
Teva Investigational Site 15165 The Bronx New York 10455 —
Teva Investigational Site 15181 Charlotte North Carolina 28277 —
Teva Investigational Site 15179 Elizabeth City North Carolina 27909 —
Teva Investigational Site 15193 Greensboro North Carolina 27410 —
Teva Investigational Site 15153 Monroe North Carolina 28112 —
Teva Investigational Site 15168 Raleigh North Carolina 27607 —
Teva Investigational Site 15173 Cincinnati Ohio 45231 —
Teva Investigational Site 15131 Toledo Ohio 43617 —
Teva Investigational Site 15201 Edmond Oklahoma 73034 —
Teva Investigational Site 15204 Tulsa Oklahoma 74133 —
Teva Investigational Site 15180 Medford Oregon 97504 —
Teva Investigational Site 15172 Portland Oregon 97239 —
Teva Investigational Site 15192 Jenkintown Pennsylvania 19046 —
Teva Investigational Site 15185 Pittsburgh Pennsylvania 15241 —
Teva Investigational Site 15161 Clinton South Carolina 29325 —
Teva Investigational Site 15159 Rock Hill South Carolina 29732 —
Teva Investigational Site 15162 Austin Texas 78759 —
Teva Investigational Site 15138 Dallas Texas 75231 —
Teva Investigational Site 15154 Dallas Texas 75231 —
Teva Investigational Site 15171 Denton Texas 76210 —
Teva Investigational Site 15155 El Paso Texas 79903-3508 —
Teva Investigational Site 15189 Houston Texas 77030 —
Teva Investigational Site 15184 Houston Texas 77070 —
Teva Investigational Site 15199 Houston Texas 77084 —
Teva Investigational Site 15191 Houston Texas 77087 —
Teva Investigational Site 15160 McKinney Texas 75069 —
Teva Investigational Site 15197 San Antonio Texas 78258 —
Teva Investigational Site 15195 Williamsburg Virginia 23188 —
Teva Investigational Site 15150 Bellingham Washington 98225 —
Teva Investigational Site 15142 Greenfield Wisconsin 53228 —

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04847674, 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 Jun 7, 2023 · Synced Sep 28, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04847674 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →