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Completed Phase 3 Interventional Results available

Study of Efficacy and Safety of Canakinumab Treatment for CRS in Participants With COVID-19-induced Pneumonia

ClinicalTrials.gov ID: NCT04362813

Public ClinicalTrials.gov record NCT04362813. 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 Jul 22, 2026, 2:42 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

Phase 3 Multicenter, Randomized, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of Canakinumab on Cytokine Release Syndrome in Patients With COVID-19-induced Pneumonia (CAN-COVID)

Study identification

NCT ID
NCT04362813
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
454 participants

Conditions and interventions

Interventions

  • Canakinumab Drug
  • Placebo Drug

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
Apr 29, 2020
Primary completion
Sep 15, 2020
Completion
Dec 21, 2020
Last update posted
Jan 23, 2022

2020

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
13
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35294
Novartis Investigative Site Glendale California 91206
Novartis Investigative Site San Francisco California 94110
Novartis Investigative Site San Francisco California 94143
Novartis Investigative Site Chicago Illinois 60611
Novartis Investigative Site Baltimore Maryland 21201
Novartis Investigative Site Boston Massachusetts 02115
Novartis Investigative Site Boston Massachusetts 02118
Novartis Investigative Site Brooklyn New York 11219
Novartis Investigative Site Chapel Hill North Carolina 27599
Novartis Investigative Site Cleveland Ohio 44106-5000
Novartis Investigative Site Philadelphia Pennsylvania 19140
Novartis Investigative Site Houston Texas 77030
Novartis Investigative Site Richmond Virginia 23298
Novartis Investigative Site Tacoma Washington 98405

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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04362813, 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 Jan 23, 2022 · Synced Jul 22, 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 protocol, eligibility criteria, and contact information for NCT04362813 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →