|
AlloNK®, an Allogeneic Non-genetically Modified, Cord Blood-derived NK Cell Therapy, in Combination With Rituximab, Studied in Relapsing Forms of B-cell Dependent Rheumatologic Diseases.
RECRUITINGPhase 2Sponsored by Artiva Biotherapeutics, Inc.
Actively Recruiting
PhasePhase 2
SponsorArtiva Biotherapeutics, Inc.
Started2025-07-09
Est. completion2028-01
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations16 sites
View on ClinicalTrials.gov →
NCT06991114
Summary
A Basket Trial of Refractory Rheumatoid Arthritis (RA), Sjögren's Disease (SjD), Idiopathic Inflammatory Myopathies (IIMs) and Systemic Sclerosis (SSc) subjects to evaluate the safety and efficacy of AlloNK, a non-genetically modified allogeneic NK cell, in combination with rituximab.
Eligibility
Age: 18 Years+Healthy volunteers accepted
For Subjects with Refractory Rheumatoid Arthritis (RA): * Documented diagnosis of RA, meeting the 2010 ACR/EULAR classification criteria. * Rheumatoid Factor (RF) or Anti Citrullinated Protein Antibody (ACPA) positive. * High-sensitivity C-reactive protein (hs-CRP) \> 3 mg/L or Erythrocyte Sedimentation Rate (ESR) \> 28 mm/hr. * Have had prior treatment for a period of at least 12 weeks with a biologic disease modifying anti-rheumatic drug and were deemed refractory by the treating physician. * Minimum of six swollen joint counts (SJC) and six tender joint counts (TJC) according to joint assessment. For subjects with Sjögren's Disease (SjD) * Prior diagnosis of Primary SjD as per 2016 ACR/EULAR criteria with confirmatory diagnosis in the 24 weeks preceding screening. * Total Clinical European League Against Rheumatism Sjogren's Syndrome Disease Activity Index (clinESSDAI) \> 6. * Salivary Flow Rate \> 0.1 mL/min on stimulation. For subjects with Idiopathic Inflammatory Myopathies (IIMs) * Presence of a positive autoantibody (ANA \>1:80 or RNP or SSA/SSB or other myositis specific autoantibodies. * Refractory IIM as defined by inadequate response/intolerance to at least 3 months of glucocorticoids and/or at least one other immunosuppressive. * Muscle biopsy or muscle MRI to confirm IIM diagnosis, where applicable, within 12 months prior to enrollment. For Subjects with Systemic Sclerosis (SSc) * Diagnosis of SSc in accordance with the ACR/EULAR 2013 classification. * Modified Rodnan skin score (mRSS) \> 10. * Initial confirmatory diagnosis within 8 years of screening. * Refractory SSc as defined by inadequate response/intolerance to at least 3 months of glucocorticoids and/or at least one other immunosuppressive.
Conditions10
ArthritisIIMIdiopathic Inflammatory Myopathies (IIMs)MyositisRefractory Rheumatoid Arthritis (RA)Rheumatoid Arthritis (RASclerodermaSjogren SyndromeSjogrens DiseaseSystemic Sclerosis (SSc)
Locations16 sites
Artiva Investigational Site Tuscaloosa
Tuscaloosa, Alabama, 35406
Artiva Investigational Site Phoenix
Phoenix, Arizona, 85037
Artiva Investigational Site Covina
Covina, California, 91723
Artiva Investigational Site Los Alamitos
Los Alamitos, California, 90720
Artiva Investigational Site Aventura
Aventura, Florida, 33180
Browse More Trials
Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
This site does not provide medical advice. Always consult your doctor before considering enrollment in a clinical trial. Learn more on our About page.
Actively Recruiting
PhasePhase 2
SponsorArtiva Biotherapeutics, Inc.
Started2025-07-09
Est. completion2028-01
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations16 sites
View on ClinicalTrials.gov →
NCT06991114