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NCT Number: NCT07115745

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

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

BMS-986515

Genetic

Specified dose on specified days

Fludarabine

Drug

Specified dose on specified days

Cyclophosphamide

Drug

Specified dose on specified days

Tocilizumab

Drug

Specified dose on specified days

Primary outcomes

  1. Number of participants with treatment-emergent adverse events (TEAEs)

    Time frame: Up to 24 months post BMS-986515 infusion

    All participants

  2. Number of participants with serious AEs (SAEs)

    Time frame: Up to 24 months post BMS-986515 infusion

    All participants

  3. Number of participants with AEs of special interest (AESIs)

    Time frame: Up to 24 months post BMS-986515 infusion

    All participants

  4. Number of participants with laboratory abnormalities

    Time frame: Up to 24 months post BMS-986515 infusion

    All participants

  5. Number of participants with Dose-Limiting Toxicities (DLTs)

    Time frame: Up to 24 months post BMS-986515 infusion

    All participants

  6. Number of participants with DLTs that occur during the DLT evaluation period

    Time frame: 28 days post-BMS-986515 infusion

    All participants

Secondary outcomes

  1. Maximum observed concentration (Cmax)

    Time frame: Up to 2 years

    All participants

  2. Area under the concentration-time curve (AUC)

    Time frame: Up to 2 years

    All participants

  3. Time of maximum observed concentration (Tmax)

    Time frame: Up to 2 years

    All participants

  4. Number of participants with interstitial lung disease (ILD) with no worsening of pulmonary function from baseline to Week 24

    Time frame: Up to 2 years

    All participants

  5. Number of participants with a humoral immune response (anti-therapeutic antibodies) against BMS-986515

    Time frame: Up to 2 years

    All participants

  6. Number of participants who achieve definition of remission in systemic lupus erythematosus (DORIS) remission at Week 24

    Time frame: Up to Week 24

    Systemic lupus erythematosus (SLE) participants

  7. Number of participants who achieve Lupus Low Disease Activity State (LLDAS) at Week 24

    Time frame: Up to Week 24

    SLE participants

  8. Change in proteinuria measured by urine protein creatinine ratio (UPCR) from baseline to Week 24

    Time frame: Up to Week 24

    SLE participants

  9. Change in Health Assessment Questionnaire-Disability Index (HAQ-DI) from baseline to Week 24

    Time frame: Up to Week 24

    SLE, systemic sclerosis (SSc), and rheumatoid arthritis (RA) participants

  10. Number of participants who achieve Myositis Response Criteria Total Improvement Score (MRC TIS) at Week 24

    Time frame: Up to Week 24

    Inflammatory myopathy (IIM) participants

  11. Change in International Myositis Outcome Assessment Collaborative Study Group (IMACS) outcome measure set for disease activity at week 24 from baseline

    Time frame: Up to Week 24

    IIM participants

  12. Change in Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI) at week 24 from baseline

    Time frame: Up to Week 24

    Dermatomyositis (DM) participants only

  13. Number of participants who achieve an minimal clinically important differences in SSc (MCID) from baseline of the modified Rodnan Skin Score (mRSS) at Week 24

    Time frame: Up to Week 24

    SSc participants

  14. Change from baseline of the Revised Composite Response Index in Systemic Sclerosis (CRISS) at Week 24

    Time frame: Up to Week 24

    SSc participants

  15. Number of participants with low disease activity at Week 24 from baseline

    Time frame: Up to Week 24

    RA participants

Study contacts

Contact information is provided by the study sponsor or research team.

BMS Clinical Trials Contact Center www.BMSClinicalTrials.com

CONTACT

[email protected]

855-907-3286

First line of the email MUST contain NCT # and Site #.

CONTACT

Sponsors and collaborators

Lead sponsor

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

Industry

Registry information

Official study 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

Important dates

Study start
2025
Primary completion
2029
Study completion
2030
First posted
Aug 11, 2025
Registry last updated
Jul 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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