Recruiting
Phase 1

BMS-986515

Sponsor:

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

Code:

NCT07115745

Conditions

Refractory Autoimmune Diseases

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

BMS-986515

Fludarabine

Cyclophosphamide

Tocilizumab

Study Details

Brief summary:

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.

Conditions

Refractory Autoimmune Diseases

Study ID

NCT07115745

Start date

Sep 4, 2025

Status verified date

Jul, 2026

Completion date

Aug 16, 2030

Anticipated

Primary completion date

Mar 15, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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.

Study Design

Enrollment

125 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: BMS-986515 Administration

Interventions

BMS-986515

Specified dose on specified days

Fludarabine

Specified dose on specified days

Cyclophosphamide

Specified dose on specified days

Tocilizumab

Specified dose on specified days

Primary outcome measure

  • Number of participants with treatment-emergent adverse events (TEAEs) [ Time Frame: Up to 24 months post BMS-986515 infusion ]
  • Number of participants with serious AEs (SAEs) [ Time Frame: Up to 24 months post BMS-986515 infusion ]
  • Number of participants with AEs of special interest (AESIs) [ Time Frame: Up to 24 months post BMS-986515 infusion ]
  • Number of participants with laboratory abnormalities [ Time Frame: Up to 24 months post BMS-986515 infusion ]
  • Number of participants with Dose-Limiting Toxicities (DLTs) [ Time Frame: Up to 24 months post BMS-986515 infusion ]
  • Number of participants with DLTs that occur during the DLT evaluation period [ Time Frame: 28 days post-BMS-986515 infusion ]

Central Contacts and Locations

Central contacts

BMS Clinical Trials Contact Center www.BMSClinicalTrials.com

855-907-3286Clinical.Trials@bms.com

Locations

Brigham And Womens Hospital

Recruiting

Boston, Massachusetts, United States, 02115

Contacts

Neda Shahriari, Site 0041

617-732-4918

Duke University

Recruiting

Durham, North Carolina, United States, 27705-2771

Contacts

Ankoor Shah, Site 0037

919-681-5698

More Information

Sponsor

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

Last update posted

Jul 14, 2026

Last verified

Jul, 2026

Keywords

  • CAR-T
  • Cell Therapy
  • Autoimmune disease
  • Systemic lupus erythematosus
  • idiopathic inflammatory myopathy
  • systemic sclerosis
  • rheumatoid arthritis
  • Musculoskeletal Diseases
  • Myositis
  • Lupus Erythematosus, Systemic
  • Scleroderma, Systemic
  • Scleroderma, Diffuse
  • Autoimmune Diseases
  • Sclerosis
  • Skin Diseases
  • Connective tissue diseases
  • BMS-986515
  • Allogeneic CAR T
  • CD19 Allogeneic CAR T
  • AlloCAR T, Cell Therapy
  • CAR T
  • SLE
  • Lupus Nephritis
  • SSc
  • IIM
  • Polymyositis
  • Dermatomyositis
  • RA

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Juno Therapeutics, Inc., a Bristol-Myers Squibb Company on 2026-07-14.