A Study of KITE-363 in Participants With Refractory Autoimmune Diseases

ID#: NCT07038447

Age: 18 years - 66+

Gender: All

Healthy Subjects: No

Study Phase: Phase 1

Recruitment Status: Enrolling by invitation

Start Date: July 02, 2025

End Date: July 01, 2029

Summary: This study will have two Phases: Phase 1a and Phase 1b. The goal of this clinical study is to learn more about the study drug KITE-363, to establish dosing, tolerability, safety, and preliminary efficacy of KITE-363 in participants with refractory autoimmune diseases. The primary objectives of this study are: Phase 1a: To evaluate the safety and tolerability of KITE-363 in participants with autoimmune disease. To determine the recommended dose for Phase 1b. Phase 1b: To evaluate the safety and efficacy of KITE-363 in participants with autoimmune disease.
Eligibility: Key

Inclusion Criteria: Inclusion Criteria for systemic lupus erythematosus (SLE) and lupus nephritis (LN):

- Age ≥ 18 years

- Meet the European Alliance of Associations for Rheumatology (EULAR)- American College of Rheumatology (ACR) 2019 classification criteria for SLE

- Presence of either double-stranded deoxyribonucleic acid (DNA) anti- double-stranded DNA (anti-dsDNA) and/or anti-Smith antibodies at screening per local laboratory.

- Moderate to severe, active disease defined as at least one British Isles Lupus Assessment Group (BILAG-A) score or 2 BILAG B (excluding constitutional and/or neuropsychiatric organ system).

- Refractory to steroids and inadequate response or intolerance to at least 2 of the following treatments, used for at least 3 months each: cyclophosphamide, mycophenolate mofetil or its derivatives, belimumab, anifrolumab, rituximab, obinutuzumab, methotrexate, azathioprine, cyclosporin, tacrolimus, or voclosporin.

- For LN: Refractory to steroids and inadequate response or intolerance to at least 2 of the following treatments, used for at least 3 months each: cyclophosphamide, mycophenolate mofetil or its derivatives, belimumab, rituximab, obinutuzumab, azathioprine, cyclosporin, tacrolimus, or voclosporin Inclusion Criteria for LN:

- Renal biopsy-proven Class III or intravenous (IV) ± V LN according to the revised International Society of Nephrology and Renal Pathology Society (ISN/RPS) criteria within 6 months prior to or during screening

- Evidence of active LN at screening Inclusion Criteria for systemic sclerosis (SSc):

- Age ≥ 18 years

- Diffuse Systemic Sclerosis (SSc) according to ACR/EULAR 2013 classification criteria with active skin disease and/or progressive SSc-interstitial lung disease (ILD) OR limited SSc with progressive ILD.

- Refractory or intolerance to 1 of the following for a minimum of 3 months and/or contraindication: mycophenolate mofetil or its derivatives, methotrexate, tocilizumab (or other IL-6 inhibitor), rituximab (or other B-cell depleting agent), nintedanib (or other antifibrotic agents), cyclophosphamide.

- High-resolution computer tomography (HRCT) scan and pulmonary function test (PFT) within 3 months prior to screening. Inclusion Criteria for idiopathic inflammatory myopathy (IIM):

- Age ≥ 18 years

- Probable or definite IIM based on EULAR/ACR 2017 classification (excluding inclusion body myositis).

- Active disease demonstrated by electromyography (EMG), magnetic resonance imaging (MRI) or muscle enzymes

- Moderate to severe disease activity

- Positive for myositis specific antibodies for patients with non-dermatomyostitis IIM

- HRCT scan and PFT within 3 months prior to screening.

- Refractory or intolerance to at least 1 month of glucocorticoids and standardized use of at least 2 immunosuppressant/modulator (eg, intravenous gamma globulins, methotrexate, mycophenolate mofetil and its derivatives, azathioprine, cyclophosphamide, calcineurin inhibitors, Janus kinase (JAK) inhibitors, rituximab or other B-cell depleting agent). Inclusion Criteria for all Cohorts:

- Adequate hepatic, renal, pulmonary, and cardiac function. Key

Exclusion Criteria: Exclusion Criteria for all Cohorts:

- Females of childbearing potential who are pregnant or breast feeding.

- Dialysis within the past year.

- History of malignancy, within the last 5 years.

- Hypogammaglobulinemia requiring immunoglobulin replacement.

- History of autologous or allogeneic stem cell transplant and/or organ transplant.

- Prior treatment with cellular therapy, gene therapy and/or T-cell engager therapy.

- Known history of HIV infection, or hepatitis B or C virus infections.

- Active or untreated latent tuberculosis (TB).

- Active or uncontrolled infections.

- Nonspecific, overlap, mixed autoimmune diseases not clearly identified into any of the studied cohorts. Exclusion Criteria for LN:

- Significant pre-existing damage or rapidly progressive glomerulonephritis (GN). Exclusion Criteria for SLE:

- Drug-induced SLE.

- Catastrophic antiphospholipid syndrome.

- Thrombotic thrombocytopenic purpura.

- Active or unstable lupus neuropsychiatric manifestations within last 6 months. Exclusion Criteria for SSc:

- Infected digital ulceration or necrosis with signs of infection.

- Severe pulmonary hypertension.

- History of systemic sclerosis renal crisis within 12 months prior to enrollment.

- History of active bleeding related to gastric antral vascular ectasia. Exclusion Criteria for IIM:

- Other inflammatory and noninflammatory myopathies.

- Severe, irreversible muscle damage. Note: Other protocol defined Inclusion/Exclusion criteria may apply.