Status:
TERMINATED
A Study to Assess the Efficacy and Safety of Namilumab in Participants With Chronic Pulmonary Sarcoidosis
Lead Sponsor:
Kinevant Sciences GmbH
Conditions:
Sarcoidosis, Pulmonary
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
This is a randomized, double-blind, placebo-controlled study with an open-label extension (OLE).
Detailed Description
This is a randomized, double-blind, placebo-controlled study with an OLE. Participants will be randomized to receive namilumab or placebo in the 26-week Double-blind Treatment Period of the study. Na...
Eligibility Criteria
Inclusion
- Inclusion Criteria :
- Male or female age ≥18 years
- Able and willing to provide written informed consent, which includes compliance with study requirements and restrictions listed in the consent form
- Greater than or equal to 6-month history of documented sarcoidosis including histological confirmation in the subject's medical records
- Evidence of sarcoidosis as indicated by: a) HRCT consistent with Pulmonary Sarcoidosis AND; b) Medical Research Council Dyspnea scale \>1 (i.e., Grade 2 or more) AND; c) One or more of the following is present: i) Screening FDG-PET scan consistent with active pulmonary sarcoidosis AND SUVmax ≥ 3; ii) Recent history of worsening sarcoidosis; iii) Recent history that tapering OCS and/or ISTs resulted in an increase of pulmonary disease
- Body Mass Index (BMI) ≤ 40 kg/m2 at Screening
- Vaccinations for COVID-19 with completion of the primary series at least 2 weeks prior to randomization
- Exclusion Criteria
- Hospitalized for any respiratory illness ≤ 30 days prior to or during Screening
- Greater than or equal to 20% fibrosis as indicated on HRCT-scan assessed by central read prior to randomization
- Hemoglobin ≤ 9.5 g/dL
- Participation in another interventional clinical trial (IP/Device) within 6 months prior to Screening, during screening and throughout the duration of the study
- ECG abnormalities that warrant further clinical investigation or management at Screening
- Systolic blood pressure (SBP) \<90 or \>180mm Hg; Diastolic blood pressure (DBP) \<60 or \>110 mm Hg at Screening
- Has documented laboratory-confirmed SARS-CoV-2 infection with pulmonary involvement or signs/symptoms of long COVID as determined by approved testing ≤ 6 months prior to randomization
- Other significant pulmonary disease or conditions that prevent subject from performing acceptable spirometry
- Females who are pregnant or breastfeeding or intend to be during the course of the study
- Any other acute or chronic medical condition, psychiatric condition, or laboratory abnormality, that in the judgment of the Investigator or Sponsor, may increase the risk associated with study participation or investigational product administration, or may interfere with the interpretation of study results, and would make the participant inappropriate for entry into this study
- Subjects who are treatment naive
- Other protocol-defined inclusion/exclusion criteria apply.
Exclusion
Key Trial Info
Start Date :
August 31 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 9 2025
Estimated Enrollment :
107 Patients enrolled
Trial Details
Trial ID
NCT05314517
Start Date
August 31 2022
End Date
April 9 2025
Last Update
September 12 2025
Active Locations (47)
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1
Kinevant Study Site
Birmingham, Alabama, United States, 35233
2
Kinevant Study Site
Palo Alto, California, United States, 94304
3
Kinevant Study Site
Valencia, California, United States, 91355
4
Kinevant Study Site
Denver, Colorado, United States, 80206