BMS-986515
GeneticSpecified dose on specified days
NCT Number: NCT07115745
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 1
Local Institution - 0007, Camperdown, New South Wales, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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.
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.
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.
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
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.
i) Participants who have SLE because of drugs or have other autoimmune diseases along with SLE.
i) Participants who have other forms of myopathies other than IIM. ii) Severe muscle damage.
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.
i) People who have additional autoimmune diseases along with RA.
Specified dose on specified days
Specified dose on specified days
Specified dose on specified days
Specified dose on specified days
Time frame: Up to 24 months post BMS-986515 infusion
All participants
Time frame: Up to 24 months post BMS-986515 infusion
All participants
Time frame: Up to 24 months post BMS-986515 infusion
All participants
Time frame: Up to 24 months post BMS-986515 infusion
All participants
Time frame: Up to 24 months post BMS-986515 infusion
All participants
Time frame: 28 days post-BMS-986515 infusion
All participants
Time frame: Up to 2 years
All participants
Time frame: Up to 2 years
All participants
Time frame: Up to 2 years
All participants
Time frame: Up to 2 years
All participants
Time frame: Up to 2 years
All participants
Time frame: Up to Week 24
Systemic lupus erythematosus (SLE) participants
Time frame: Up to Week 24
SLE participants
Time frame: Up to Week 24
SLE participants
Time frame: Up to Week 24
SLE, systemic sclerosis (SSc), and rheumatoid arthritis (RA) participants
Time frame: Up to Week 24
Inflammatory myopathy (IIM) participants
Time frame: Up to Week 24
IIM participants
Time frame: Up to Week 24
Dermatomyositis (DM) participants only
Time frame: Up to Week 24
SSc participants
Time frame: Up to Week 24
SSc participants
Time frame: Up to Week 24
RA participants
Contact information is provided by the study sponsor or research team.
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com
CONTACT
First line of the email MUST contain NCT # and Site #.
CONTACT
Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
Industry
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
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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