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Terminated Phase 2 Interventional Accepts healthy volunteers Results available

A Study to Assess the Safety, Tolerability, and Efficacy of Namilumab in Participants With Active Cardiac Sarcoidosis

ClinicalTrials.gov ID: NCT05351554

Public ClinicalTrials.gov record NCT05351554. 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 21, 2026, 8:19 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 Randomized, Double-blind, Placebo-controlled, Phase 2a Study With an Open-label Cohort to Assess the Safety, Tolerability, and Efficacy of Namilumab in Subjects With Active Cardiac Sarcoidosis

Study identification

NCT ID
NCT05351554
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Kinevant Sciences GmbH
Industry
Enrollment
1 participant

Conditions and interventions

Interventions

  • Namilumab Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 22, 2022
Primary completion
Nov 14, 2022
Completion
Dec 12, 2022
Last update posted
Apr 16, 2025

2022

United States locations

U.S. sites
12
U.S. states
12
U.S. cities
12
Facility City State ZIP Site status
Kinevant Study Site Palo Alto California 94304
Kinevant Study Site Denver Colorado 80206
Kinevant Study Site New Haven Connecticut 06519
Kinevant Study Site Gainesville Florida 32610
Kinevant Study Site Iowa City Iowa 52242
Kinevant Study Site Baltimore Maryland 21234
Kinevant Study Site Boston Massachusetts 02115
Kinevant Study Site Ann Arbor Michigan 48109
Kinevant Study Site New York New York 10029
Kinevant Study Site Cleveland Ohio 44195
Kinevant Study Site Portland Oregon 97239
Kinevant Study Site Charleston South Carolina 29425

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 NCT05351554, 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 Apr 16, 2025 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05351554 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →