AD-PluReceptor NK Cells plus Tafasitamab-Cxix and Lymphodepleting Chemotherapy for the Treatment of Patients with Systemic Sclerosis or System Lupus Erythematosus
This phase I/II trial tests the safety, side effects and best dose of AD-PluReceptor natural killer (NK) cells plus tafasitamab-cxix and lymphodepleting chemotherapy, with fludarabine and cyclophosphamide, for the treatment of patients with systemic sclerosis or systemic lupus erythematosus. AD-PluReceptor-NK cells are genetically engineered cells created from umbilical cord blood to attack cells involved in autoimmune disorders such as systemic sclerosis or systemic lupus erythematosus. Giving chemotherapy with tafasitamab-cxix, fludarabine and cyclophosphamide may help kill autoimmune cells in the body to prepare for the AD-PluReceptor NK cells. Giving PluReceptor NK cells plus tafasitamab-cxix and lymphodepleting chemotherapy may be safe and tolerable in treating patients with systemic sclerosis or systemic lupus erythematosus.
Inclusion Criteria
- SYSTEMIC SCLEROSIS: Diagnosis of systemic sclerosis (SSc) defined as follows: * Fulfilling 2013 American College of Rheumatology (ACR) and European League Against Rheumatism classification (EULAR) criteria for SSc * Antinuclear antibody (ANA) by immunofluorescence positive at titer ≥ 1:80 at screening or prior to screening
- SYSTEMIC SCLEROSIS: SSc disease activity * Diffuse SSc meeting the following criteria: ** Disease duration ≤ 5 years (from onset of first non-Raynaud manifestation) AND ** Modified Rodnan Skin Score (mRSS) ≥ 15 at screening * Participants diagnosed with diffuse or limited cutaneous SSc AND progressive interstitial lung disease (ILD) on high resolution computed tomography (HRCT) and ≤ 5 years duration (from onset of first non-Raynaud manifestation) defined by either (1) or (2) ** Progressive ILD as defined by Raghu et al (≥ 2 of the following): *** Worsening respiratory symptoms *** Physiological evidence of disease progression (≥ 1 of the following): **** Absolute decline in forced vital capacity (FVC) ≥ 5% predicted within 1 year of follow-up **** Absolute decline in diffuse lung carbon monoxide (DLCO) (corrected for hemoglobulin [Hb]) ≥ 10% predicted within 1 year of follow-up radiological evidence of disease progression **** Increased extent or severity of traction bronchiectasis and bronchiolectasis **** New ground-glass opacity with traction bronchiectasis **** New fine reticulation **** Increased extent or increased coarseness of reticular abnormality **** New or increased honeycombing **** Increased lobar volume loss ** FVC < 80% predicted and moderate to severe ILD, as assessed by a radiologist
- SYSTEMIC SCLEROSIS: Inadequate response to at least 2 of the following treatments used for at least 3 months: mycophenolate, cyclophosphamide, rituximab, and/or tocilizumab
- SYSTEMIC LUPUS ERYTHEMATOSUS: A clinical diagnosis of systemic lupus erythematosus (SLE), based on the 2019 European League Against Rheumatism (EULAR)/ American College of Rheumatology (ACR) classification criteria for adult SLE
- SYSTEMIC LUPUS ERYTHEMATOSUS: Positive anti-nuclear antibody (ANA) titer ≥1:80 or positive anti-double strand deoxyribonucleic acid (dsDNA) antibody at screening
- SYSTEMIC LUPUS ERYTHEMATOSUS (LUPUS NEPHRITIS [LN] ONLY): Active, biopsy-proven lupus nephritis class III or IV, with or without the presence of Class V, using the 2018 Revised International Society of Nephrology/Renal Pathology Society criteria
- SYSTEMIC LUPUS ERYTHEMATOSUS: Diagnosed with active SLE. Subjects with either LN or without LN will be eligible if they meet the following criteria: * For LN subjects: Urine protein-to-creatinine ratio (UPCR) ≥ 1 mg/mg on 2 first morning void urine samples during screening despite prior or current treatment with standard of care therapy for at least 12 weeks, including corticosteroids, mycophenolate mofetil (MMF)/mycophenolic acid (MPA), cyclophosphamide (CY), calcineurin inhibitors, belimumab, and/or rituximab. * For non-renal SLE subjects: Systemic Lupus Erythematosus Disease Activity Index (SLEDAI)-2K ≥ 8 and clinical SLEDAI-2K ≥ 6 (excluding headache, alopecia, mucosal ulcers, fever, and organic brain syndrome) during screening despite prior or current treatment with standard of care therapy, including corticosteroids, rituximab or other B cell depleting agents, CY, MMF/MPA, azathioprine, methotrexate, 6-mercaptopurine, sirolimus, tacrolimus, thalidomide, leflunomide, mizorbine, anifrolumab, and/or belimumab
- SYSTEMIC LUPUS ERYTHEMATOSUS: If a subject is currently receiving: * Standard immunosuppressive therapy (including MMF/MPA, CY, azathioprine, antimalarial therapy, methotrexate, 6-mercaptopurine, sirolimus, tacrolimus, thalidomide, leflunomide, or mizorbine), the therapy must have been initiated at least 12 weeks prior to screening and on a stable dose for at least 8 weeks prior to screening, except for dose reduction due to safety or tolerability. * A renin-angiotensin-aldosterone inhibitor, (including direct renin inhibitors, angiotensin converting enzyme [ACE] inhibitors, angiotensin receptor blockers [ARBs], and mineralocorticoid receptor blockers), the subject must be on a stable dose for at least 8 weeks prior to screening. A sodium-glucose cotransporter-2 (SGLT2) inhibitor, the subject must be on a stable dose for at least 8 weeks prior to screening. * Regarding oral corticosteroid, doses < 0.5 mg/kg prednisone equivalent at the time of infusion are required
- SYSTEMIC LUPUS ERYTHEMATOSUS: Adequate renal function, defined as: * For LN subjects: Estimated glomerular filtration rate of ≥ 45 mL/min/1.73m^2 using the chronic kidney disease-epidemiology equation. * For non-renal SLE subjects: Estimated glomerular filtration rate of ≥ 60 mL/min/1.73m^2 using the chronic kidney disease-epidemiology equation
- Able to provide informed consent
- Age ≥ 18 to ≤ 65 years
- All subjects should be up to date on age-appropriate recommended vaccinations, including against coronavirus 2019 (COVID-19/SARS-CoV-2), as per Centers for Disease Control and Prevention (CDC) or institutional guidelines for immune-compromised individuals vaccination requirement
- Peripheral blood absolute neutrophil count (ANC) ≥ 1 × 10^9/L, unless the neutropenia is deemed to be caused by the underlying autoimmune disease
- Hemoglobin ≥ 8 g/dl, unless the anemia is deemed to be caused by the underlying autoimmune disease
- Platelet count ≥ 50 × 10^9/L without platelet transfusion support, unless the thrombocytopenia is deemed to be caused by the underlying autoimmune disease. No clinically significant active bleeding
- Aspartate aminotransferase (AST) / alanine aminotransferase (ALT) ≤ 1.5 × upper limit of normal (ULN) and total bilirubin < 1.5 × ULN (or direct bilirubin < 1.5× ULN with documented Gilbert’s syndrome)
- Oxygen saturation (SaO2) ≥ 92% on room air
- Adequate cardiac function, defined as left ventricular ejection fraction (LVEF) ≥ 45% as assessed by echocardiogram (ECHO) or multigated acquisition (MUGA) scan
- Recovery to ≤ grade 1 or baseline of any non-hematological toxicities due to prior therapy
- Negative pregnancy test in women of child bearing potential (WOCBP)
- All participants who are able to have children must practice effective birth control while on study and up to 3 months post completion of therapy. Acceptable forms of birth control for female patients include hormonal birth control, intrauterine device, diaphragm with spermicide, condom with spermicide, or abstinence, for the length of the study. If the participant is a female and becomes pregnant or suspects pregnancy, she must immediately notify her doctor. If the participant becomes pregnant during this study, she will be taken off this study. Men who are able to have children must use effective birth control while on the study. If the male participant fathers a child or suspects that he has fathered a child while on the study, he must immediately notify his doctor. Participant is willing and able to adhere to the study visit schedule and other protocol requirements and willing to sign informed consent.
Exclusion Criteria
- SYSTEMIC SCLEROSIS: SSc related pulmonary arterial hypertension (PAH) requiring active treatment
- SYSTEMIC SCLEROSIS: Rapidly progressive SSc related lower gastrointestinal (GI) (small and large intestines) involvement (requiring parenteral nutrition); active gastric antral vascular ectasia
- SYSTEMIC SCLEROSIS: Prior scleroderma renal crisis
- SYSTEMIC SCLEROSIS: Uncontrolled or rapidly progressive ILD (FVC < 50; DLCO < 50%); oxygen saturation (SaO2) < 92% (room air at rest); or who have required mechanical breathing assistance (ventilator) within 1 year of signing informed consent
- SYSTEMIC LUPUS ERYTHEMATOSUS: Treatment with rituximab or other B cell-depleting agent within 26 weeks prior to screening, or within 12 weeks if there are laboratory results indicating presence of CD19+B cells
- SYSTEMIC LUPUS ERYTHEMATOSUS: Treatment with voclosporin or other calcineurin inhibitor within 8 weeks prior to screening
- SYSTEMIC LUPUS ERYTHEMATOSUS: Treatment with anifrolumab, belimumab, or other biologic agent within 12 weeks prior to screening
- SYSTEMIC LUPUS ERYTHEMATOSUS (LN ONLY): For LN subjects only: Evidence of severe chronicity on kidney biopsy, defined as a modified National Institute of Health chronicity index score of 3+ for any of the following individual biopsy features: total glomerulosclerosis score, fibrous crescents, tubular atrophy, or interstitial fibrosis
- SYSTEMIC LUPUS ERYTHEMATOSUS: A diagnosis of antiphospholipid antibody syndrome by the 2006 Revised Sapporo International Consensus Criteria at the time of screening
- SYSTEMIC LUPUS ERYTHEMATOSUS: The presence of biopsy-proven kidney disease other than active lupus nephritis
- SYSTEMIC LUPUS ERYTHEMATOSUS: Moderate-to-severe chronic pulmonary disease, including asthma requiring or refractory to medium or high-dose inhaled corticosteroids combined with other longer-acting medications, In subjects who have had pulmonary function tests: Spirometry results of forced expiratory volume (FEV1)/forced vital capacity < 0.7 and FEV1 < 80% predicted after bronchodilators, or diffusing capacity of the lungs for carbon monoxide results < 60% predicted
- SYSTEMIC LUPUS ERYTHEMATOSUS: Active, severe cardiac manifestations of SLE, including constrictive pericarditis, hemodynamically significant pericardial effusions, and myocarditis at the time of screening
- Other systemic autoimmune diseases (e.g., multiple sclerosis, psoriasis, inflammatory bowel disease, etc.) are excluded. Participants with type I autoimmune diabetes mellitus, thyroid autoimmune disease, Celiac disease, or secondary Sjögren’s syndrome are not excluded
- Uncontrolled medical, psychological, familial, sociological, or geographical conditions that do not permit compliance with the protocol, as judged by the Investigator; or unwillingness or inability to follow the procedures required in the protocol
- Active, clinically significant central nervous system pathology
- Prior history of malignancies or lymphoproliferative disease, following are allowed: Basal or squamous cell carcinoma of the skin, carcinoma in situ of the cervix or breast. History of malignancy that has been treated with a curative intent and is in remission > 2 years may be allowed after discussion with principal investigator (PI)
- Active hepatitis B, active hepatitis C, active syphilis, any human immunodeficiency virus (HIV), human lymphocytic T-cell virus type 1 and/or type 2 (HTLV-1 and/or HTLV-2)
- Uncontrolled or active systemic fungal, bacterial, viral, or other infection despite appropriate anti-infective treatment at screening or within 72 hours before LD chemotherapy, or 5 days before AD-PluReceptor administration
- History of any one of the following cardiovascular conditions within the 6 months prior to screening: Class III or IV heart failure as defined by the New York Heart Association, myocardial infarction, unstable angina, or other clinically significant cardiac disease
- Prior CAR T cell therapy, genetically modified T cell therapy, concurrent immunosuppressive drugs, e.g., mycophenolate mofetil, systemic steroids, tocilizumab. Immunosuppressive medications are allowed if not being used for management of SLE, LN or SSc
- History of anaphylactic or severe systemic reaction to fludarabine (FLU), cytarabine (CY), or any of their metabolites
- Active infection requiring medical intervention at screening
- Current symptoms of severe, progressive, or uncontrolled renal, hepatic, hematological, gastrointestinal (on total parenteral nutrition [TPN]), pulmonary, psychiatric, cardiac, neurological, or cerebral disease, including severe and uncontrolled infections, such as sepsis and opportunistic infections
- Concomitant medical conditions that, in the opinion of the investigator, might place the subject at unacceptable risk for participation in this study, interfere with the assessment of the effects or safety of the investigational product or with the study procedures
- Autoimmune disorder other than SLE or SSc requiring immunosuppressive therapies
Additional locations may be listed on ClinicalTrials.gov for NCT06434363.
Locations matching your search criteria
United States
Texas
Houston
PRIMARY OBJECTIVE:
I. To determine the safety, tolerability and optimal cell dose of AD-PluReceptor plus tafasitamab cxix and lymphodepleting chemotherapy in patients with systemic sclerosis and systemic lupus erythematosus (including lupus nephritis).
SECONDARY OBJECTIVES:
I. To assess the overall response rate.
II. To evaluate the persistence and kinetics of infused allogeneic donor AD-PluReceptor cells in the recipient.
III. To conduct comprehensive immune reconstitution studies.
IV. To evaluate the number of patients not requiring any systemic immunosuppressive therapy for their autoimmune disease at 1 year post infusion.
OUTLINE: This is a phase I, dose-escalation study of AD-PluReceptor-NK cells followed by a phase II dose-expansion study.
Patients receive tafasitamab-cxix intravenously (IV) over 1.5-2.5 hours on days -3, 0, +4, +11, +18, +25, lymphodepletion chemotherapy with fludarabine and cyclophosphamide IV on days -5 to -3 and AD-PluReceptor NK cells IV over 30 minutes on day 0. Patients undergo echocardiography (ECHO) or multigated acquisition (MUGA) scan, chest x-ray and may undergo computed tomography (CT) scan during screening, and blood and urine sample collection throughout the study. Patients may also optionally undergo kidney biopsy on study.
After completion of study treatment, patients are followed up at day 3, 7, 14, 21, week 4, 8, 12, 16, month 6, 9, 12, 24 then periodically for up to 15 years.
Trial PhasePhase I/II
Trial Typetreatment
Lead OrganizationM D Anderson Cancer Center
Principal InvestigatorChitra Hosing
- Primary ID2024-0208
- Secondary IDsNCI-2024-04434
- ClinicalTrials.gov IDNCT06434363