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Completed Phase 2 Interventional Results available

TD-0903 for ALI Associated With COVID-19

ClinicalTrials.gov ID: NCT04402866

Public ClinicalTrials.gov record NCT04402866. 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 20, 2026, 9:54 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, Randomized, Double-Blind, Placebo-Controlled, Parallel-group, Multi-center Study of an Inhaled Pan-Janus Kinase Inhibitor, TD-0903, to Treat Symptomatic Acute Lung Injury Associated With COVID-19

Brief summary

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

This Phase 2 study will evaluate the efficacy, safety, pharmacodynamics and pharmacokinetics of inhaled TD-0903 compared with a matching placebo in combination with standard of care (SOC) in hospitalized patients with confirmed COVID-19 associated acute lung injury and impaired oxygenation.

Study identification

NCT ID
NCT04402866
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Theravance Biopharma
Industry
Enrollment
235 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 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
Jun 24, 2020 (Actual)
Primary completion
Apr 21, 2021 (Actual)
Completion
Apr 21, 2021 (Actual)
Last update posted
Mar 17, 2022

2020 – 2021

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Theravance Biopharma Investigational Site Duarte California 91010 —
Theravance Biopharma Investigational Site Denver Colorado 80220 —
Theravance Biopharma Investigational Site Sebring Florida 33870 —
Theravance Biopharma Investigational Site Boston Massachusetts 02135 —
Theravance Biopharma Investigational Site Fall River Massachusetts 02720 —
Theravance Biopharma Investigational Site Kalispell Montana 59901 —
Theravance Biopharma Investigational Site Glens Falls New York 12801 —
Theravance Biopharma Hyde Park New York 11040 —
Theravance Biopharma Investigational Site Columbus Ohio 43214 —
Theravance Biopharma Investigational Site Allentown Pennsylvania 18103 —
Theravance Biopharma Investigational Site Bethlehem Pennsylvania 18015 —
Theravance Biopharma Investigational Site Wenatchee Washington 98801 —

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04402866, 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 17, 2022 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04402866 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →