A Study of Healthy Donor CD19-targeted Allogeneic CAR T Cells in Participants With Severe, Refractory Autoimmune Diseases
Recruiting · NCT07115745 · Interventional (participants receive a specific treatment) · Lead sponsor: Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
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 take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 1
Study type
Interventional (participants receive a specific treatment)
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.
Where it is running
28 locations listed across 2 US states.
- Brigham And Womens Hospital - Boston, Massachusetts, United States
- Duke University - Durham, North Carolina, United States
- Charité - Universitaetsmedizin Berlin - Campus Bejnamin Franklin - Berlin, Germany
- Fundeni Clinical Institute - Bucharest, Romania
- Universitätsklinikum Carl Gustav Carus an der TU Dresden - Dresden, Germany
- Local Institution - 0031 - Hamburg, Germany
- Hadassah Medical Center - Jerusalem, Israel
- Local Institution - 0039 - Porto Alegre, Brazil
- Revmatologicky ustav - Prague, Czechia
- Local Institution - 0038 - São Paulo, Brazil
- CHU Strasbourg-Hautepierre - Strasbourg, Alsace, France
- Hospital Universitari Vall d'Hebron - Barcelona, Barcelona [Barcelona], Spain
- Hospital de la Santa Creu i Sant Pau - Barcelona, Catalunya [Cataluña], Spain
- Sheba Medical Center - Ramat Gan, Central District, Israel
- ARENSIA Exploratory Medicine - Cluj-Napoca, Cluj, Romania
- Local Institution - 0040 - Salvador, Estado de Bahia, Brazil
- Hospital Universitario Ramón y Cajal - Madrid, Madrid, Comunidad de, Spain
- Local Institution - 0007 - Camperdown, New South Wales, Australia
- Hopital Claude Huriez - CHU de Lille - Lille, Nord, France
- Universitaetsklinikum Duesseldorf - Düsseldorf, North Rhine-Westphalia, Germany
- Uniwersyteckie Centrum Kliniczne - Gdansk, Pomeranian Voivodeship, Poland
- Local Institution - 0004 - Prague, Praha 5, Czechia
- Local Institution - 0008 - Brisbane, Queensland, Australia
- Universitaetsklinikum Schleswig-Holstein Campus Kiel - Kiel, Schleswig-Holstein, Germany
- Szpital Specjalistyczny nr 1 w Bytomiu - Bytom, Silesian Voivodeship, Poland
- Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie Panstwowy Instytut Badawczy w Gliwicach - Gliwice, Silesian Voivodeship, Poland
- Local Institution - 0013 - Clayton, Victoria, Australia
- Local Institution - 0017 - Lodz, Łódź Voivodeship, Poland