Tests donor-derived CD19 CAR T cells in people with severe autoimmune diseases
Tests donor-derived CAR T cells in adults with severe, hard-to-treat autoimmune diseases.
Key facts
- Who runs it
- Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
- Where
- Boston and Durham, United StatesSee the 2 sitesAlso in 9 other countries, 26 sites
- Trial code
- NCT07115745
- EU 2024-517681-41-00
- U1111-1308-9273
- Registry title
- A Study of Healthy Donor CD19-targeted Allogeneic CAR T Cells in Participants With Severe, Refractory Autoimmune Diseases
- Status
- Recruiting
- Phase
- Phase 1
- People taking part
- 125 people, planned
- Started
- 4 Sept 2025
- Expected to end
- 16 Aug 2030
- Type of study
- Interventional
- Treatments tested
- BMS-986515
- Fludarabine
- Cyclophosphamide
- Tocilizumab
- Record updated
- 14 July 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with severe autoimmune disease that did not respond to usual treatment: lupus, inflammatory myopathy, systemic sclerosis or rheumatoid arthritis.
- Age
- 18 years or older
- Sex
- All sexes can join.
- Disease stage
- Severe, refractory (hard to treat) disease that is active. Lupus, inflammatory myopathy, systemic sclerosis (skin and/or lung disease that is getting worse) or difficult to treat rheumatoid arthritis.
- Earlier treatment
- Poor response to, or could not tolerate, earlier treatments such as steroids and immunosuppressive therapies. Previous CAR-T cell therapy is not allowed.
- Biomarker or test result
- For lupus: positive for at least one of these antibodies at screening: anti-nuclear, anti-dsDNA, anti-histone, anti-chromatin or anti-Sm.
Main reasons for not taking part
- Any other systemic autoimmune disease
- Pregnant or nursing women
- Active hepatitis B, hepatitis C or HIV
- Past cancer, or uncontrolled or active infection
- Previous CAR-T cell therapy
The registry criteria, word for word
Show all 23 criteriaShow less
Who can take part
- Systemic lupus erythematosus (SLE) population:
- Diagnosis of SLE based on the 2019 American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR)
- 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
- Inadequate response or intolerance to steroids and immunosuppressive therapies
- Participants must have active disease at screening
- Inflammatory myopathy (IIM) population:
- Participants meeting the 2017 American College of Rheumatology (ACR) / European League Against Rheumatism (EULAR) classification criteria
- Participants must meet criteria for with severe, refractory IIM. iii) Participants who had inadequate response to steroids and prior immunosuppressive therapies
- Evidence of active disease
- Systemic sclerosis (SSc) population:
- Participant must fulfill the 2013 American College of Rheumatology (ACR)/ European League Against Rheumatism (EULAR) classification criteria for systemic sclerosis
- 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:
- 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
Who cannot take part
- Previous CAR-T cell therapy. viii) Significant lung impairment. ix) Inadequate organ function. x) Active, clinically significant, central nervous system (CNS) disorders
- 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
- SLE population:; Participants who have SLE because of drugs or have other autoimmune diseases along with SLE
- Rapidly deteriorating SSc, or history of severe kidney disease
- RA population:; People who have additional autoimmune diseases along with RA
- All participants:
- IIM population:; Participants who have other forms of myopathies other than IIM. ii) Severe muscle damage
- SSc population:; People who have high blood pressure in the arteries of the lungs caused by SSc, which needs regular treatment to keep it under control
- Other protocol-defined inclusion/exclusion criteria apply
Where in United States
Also in 9 other countries, 26 sites
- Brigham and Womens HospitalBoston, United StatesContact: Neda Shahriari, Site 0041Taking people
- Duke UniversityDurham, United StatesContact: Ankoor Shah, Site 0037Taking people
About the trial
What the trial wants to find out
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.
The group in the trial
- BMS-986515 AdministrationTreatment being tested
Treatment: BMS-986515, Fludarabine, Cyclophosphamide, and Tocilizumab
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorData and sources
- Registry record
- Listed on ClinicalTrials.gov and on the EU's official list of trials (CTIS).
- Official title
- A Phase 1, Multicenter, Open-label Study of BMS-986515, Healthy Donor Allogeneic CD19-targeted Chimeric Antigen Receptor (CAR) T Cells, in Participants With Severe, Refractory Autoimmune Diseases
- Plain-language title
- Tests donor-derived CD19 CAR T cells in people with severe autoimmune diseasesGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 12 November 2026.
- Record updated
- 14 July 2026