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Recruiting Phase 1 NCT07115745

A Study of Healthy Donor CD19-targeted Allogeneic CAR T Cells in Participants With Severe, Refractory Autoimmune Diseases

Phase 1 – testing safety in a small group of people
Conditions: Refractory Autoimmune Diseases

Sponsor: Juno Therapeutics, Inc., a Bristol-Myers Squibb Company

trial.available_in: БГ
Overview
The purpose of this study is to determine the safety, tolerability, optimal dose, and preliminary efficacy of BMS-986515, a healthy donor (HD) allogeneic CD19-targeted CART cell product, in participants with severe, refractory autoimmune diseases.
Who can participate
Inclusion Criteria \- Systemic lupus erythematosus (SLE) population:. i) Diagnosis of SLE based on the 2019 American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR). ii) Participant must be positive for at least one of the following antibodies at screening: anti-nuclear antibody, anti-dsDNA, anti-histone, anti-chromatin or anti-Sm antibody. iii) Inadequate response or intolerance to steroids and immunosuppressive therapies. iv) Participants must have active disease at screening. \- Inflammatory myopathy (IIM) population:. i) Participants meeting the 2017 American College of Rheumatology (ACR) / European League Against Rheumatism (EULAR) classification criteria. ii) Participants must meet criteria for with severe, refractory IIM. iii) Participants who had inadequate response to steroids and prior immunosuppressive therapies. iv) Evidence of active disease. \- Systemic sclerosis (SSc) population:. i) Participant must fulfill the 2013 American College of Rheumatology (ACR)/ European League Against Rheumatism (EULAR) classification criteria for systemic sclerosis. ii) Inadequate disease response or intolerance to prior therapies. iii) Participants diagnosed with progressive systemic sclerosis including skin disease and/or interstitial lung disease. \- Rheumatoid arthritis (RA) population:. i) Participants with difficult to treat RA. ii) Participants with a diagnosis of RA meeting 2010 ACR/EULAR criteria. iii) Rheumatoid arthritis disease activity at screening and baseline visit. iv) Inadequate disease response or intolerance to standard of care therapy. Exclusion Criteria \- All participants:. i) Any other systemic autoimmune disease. ii) Pregnant or nursing women. iii) Active hepatitis B, C or HIV. iv) Prior history of malignancies. v) Uncontrolled or active infection. vi) History of certain cardiovascular conditions within 6 months prior to screening. vii) Previous CAR-T cell therapy. viii) Significant lung impairment. ix) Inadequate organ function. x) Active, clinically significant, central nervous system (CNS) disorders. * SLE population:. i) Participants who have SLE because of drugs or have other autoimmune diseases along with SLE. * IIM population:. i) Participants who have other forms of myopathies other than IIM. ii) Severe muscle damage. * SSc population:. i) People who have high blood pressure in the arteries of the lungs caused by SSc, which needs regular treatment to keep it under control. ii) Rapidly deteriorating SSc, or history of severe kidney disease. * RA population:. i) People who have additional autoimmune diseases along with RA. * Other protocol-defined inclusion/exclusion criteria apply.
Locations 10
Australia (1)
Local Institution - 0007
Camperdown , New South Wales
NOT_YET_RECRUITING
Brazil (1)
Local Institution - 0040
Salvador , Estado de Bahia
NOT_YET_RECRUITING
Czech Republic (1)
Local Institution - 0004
Prague , Praha 5
NOT_YET_RECRUITING
France (1)
CHU Strasbourg-Hautepierre
Strasbourg , Alsace
Marc SCHERLINGER, Site 0005
Germany (1)
Local Institution - 0023
Düsseldorf , North Rhine-Westphalia
NOT_YET_RECRUITING
Israel (1)
Sheba Medical Center
Ramat Gan , Central District
Merav Lidar, Site 0015
Poland (1)
Uniwersyteckie Centrum Kliniczne
Gdansk , Pomeranian Voivodeship
Anna Wojteczek, Site 0019
Romania (1)
ARENSIA Exploratory Medicine
Cluj-Napoca , Cluj
Ciprian Tomuleasa, Site 0003
Spain (1)
Hospital Universitari Vall d'Hebron
Barcelona , Barcelona [Barcelona]
Alfredo Guillen-Del-Castillo, Site 0011
United States (1)
Local Institution - 0041
Boston , Massachusetts
NOT_YET_RECRUITING
Technical details
Status
Recruiting
Phase
Phase 1
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
04.09.2025
Completion date
16.08.2030
Registry ID
NCT07115745
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.