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Taking people in United StatesPhase 1

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
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

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data 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