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Completed Phase 2 Interventional Results available

Study of Efficacy and Safety of MAS825 in Patients With COVID-19

ClinicalTrials.gov ID: NCT04382651

Public ClinicalTrials.gov record NCT04382651. 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 1, 2026, 10:14 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, Randomized, Placebo-controlled, Participant and Investigator Blinded, Multi-center Study to Assess Efficacy and Safety of MAS825 for the Treatment of SARS-CoV-2 Infected Patients With COVID-19 Pneumonia and Impaired Respiratory Function

Brief summary

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

This clinical study was designed to assess the efficacy and safety of MAS825 for the treatment of severe acute respiratory syndrome coronavirus 2 (SARS-Cov-2) infected patients with coronavirus disease 2019 (COVID-19) pneumonia and impaired respiratory function.

Study identification

NCT ID
NCT04382651
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
140 participants

Conditions and interventions

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
Jun 10, 2020
Primary completion
Jan 5, 2021
Completion
Apr 20, 2021
Last update posted
Aug 9, 2022

2020 – 2021

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
20
Facility City State ZIP Site status
Novartis Investigative Site Chula Vista California 91911
Novartis Investigative Site Glendale California 91206
Novartis Investigative Site Irvine California 92697
Novartis Investigative Site La Mesa California 91942
Novartis Investigative Site Santa Monica California 90404
Novartis Investigative Site Torrance California 90503
Novartis Investigative Site Denver Colorado 80220
Novartis Investigative Site Washington D.C. District of Columbia 20037
Novartis Investigative Site Idaho Falls Idaho 83404
Novartis Investigative Site Alexandria Louisiana 71301
Novartis Investigative Site Baton Rouge Louisiana 70809
Novartis Investigative Site Lafayette Louisiana 70596
Novartis Investigative Site Boston Massachusetts 02115
Novartis Investigative Site Boston Massachusetts 02118
Novartis Investigative Site Brooklyn New York 11219
Novartis Investigative Site Asheville North Carolina 28805
Novartis Investigative Site Columbus Ohio 43214
Novartis Investigative Site Bend Oregon 97701
Novartis Investigative Site Philadelphia Pennsylvania 19140
Novartis Investigative Site Houston Texas 77030
Novartis Investigative Site Mesquite Texas 75149

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04382651, 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 Aug 9, 2022 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04382651 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →