AB-101 (also known as AlloNK) is an off-the shelf, allogeneic cell product made of "natural killer" cells, also called NK cells. White blood cells are part of the immune system and NK cells are a type of white blood cell that is known to enhance the effect of monoclonal antibody therapies. This clinical trial will enroll adult patients with lupus nephritis Class III or IV either with or without the presence of Class V who relapsed or did not respond to previous standard of care treatment approaches, or other forms of refractory systemic lupus erythematosus. The primary objective is to assess the safety, tolerability and preliminary activity of AB-101 plus a B-cell depleting mAb (e.g., rituximab, obinutuzumab) after cyclophosphamide and fludarabine in adult subjects with relapsed/refractory lupus nephritis Class III or IV, with or without the presence of Class V, or other forms of refractory systemic lupus erythematosus. Patients will be assigned to receive either AB-101 alone as monotherapy or in combination with a B-cell depleting mAb (e.g., rituximab, obinutuzumab). All patients will receive at least 1 treatment cycle of AB-101, followed by scheduled assessments of overall health and response status. Patients may receive up to 2 cycles of treatment spaced 24 weeks apart.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
51
NK Cell Therapy
Lymphodepleting chemotherapy
Lymphodepleting chemotherapy
Anti-CD20 antibody therapy
Anti-CD20 antibody therapy
Artiva Investigational Site Birmingham
Birmingham, Alabama, United States
Artiva Investigational Site Tucson
Tucson, Arizona, United States
Artiva Investigational Site San Diego
San Diego, California, United States
Artiva Investigational Site Aventura
Aventura, Florida, United States
Artiva Investigational Site Plantation
Plantation, Florida, United States
Artiva Investigational Site Iowa
Iowa City, Iowa, United States
Artiva Investigational Site Charlotte
Charlotte, North Carolina, United States
Artiva Investigational Site Mesquite
Mesquite, Texas, United States
Artiva Investigational Site Woodlands
The Woodlands, Texas, United States
Incidence of Treatment-Emergent Adverse Events and Serious Adverse Events
Incidence, severity and causality of adverse events and serious adverse events
Time frame: From the time of consent through 104 weeks after initiation of study treatment
AB-101 Clinical Activity
Determined by Overall Response Rate in subjects with lupus nephritis and refractory systemic lupus erythematosus
Time frame: From the time of first dose through 104 weeks after initiation of study treatment
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