AB-101 in Combination With B-Cell Depleting mAb in Patients Who Failed Treatment for Class III or IV Lupus Nephritis or Other Forms of Refractory Systemic Lupus Erythematosus

Last updated: August 12, 2025
Sponsor: Artiva Biotherapeutics, Inc.
Overall Status: Active - Recruiting

Phase

1

Condition

Cutaneous Lupus Erythematosus

Lupus

Lupus Nephritis

Treatment

Obinutuzumab

Fludarabine

AB-101

Clinical Study ID

NCT06265220
AB-101-03
  • Ages > 18
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria for all subjects (Lupus Nephritis or SLE)

  • Diagnosis of SLE according to the 2019 European League Against Rheumatism/AmericanCollege of Rheumatology (EULAR/ACR) Classification Criteria

  • Subjects must have had an inadequate response with at least two prior lines ofstandard of care (SoC) treatment.

Inclusion Criteria for LN:

  • Adult subjects with lupus nephritis Class III or IV (with or without the presence ofClass V)

  • Evidence of active disease on renal biopsy.

  • All subjects are required to receive adequate concomitant antihypertensive andantiproteinuric therapy with blockade of the renin-angiotensin system

Inclusion Criteria for SLE:

  • Total systemic lupus erythematosus disease activity index (SLEDAI-2K score) ≥ 8, andclinical SLEDAI-2K ≥ 4.

  • British Isles Lupus Assessment Group 2004 (BILAG-2004) activity score of A in ≥ 1organ, or a BILAG-2004 activity score of B in ≥ 2 organs.

  • Subjects have failed at least two conventional therapies

Exclusion

Exclusion Criteria:

  • Known past or current malignancy

  • Clinical evidence of significant unstable or uncontrolled acute or chronic diseasesnot due to SLE

  • Subjects with known active viral infections

  • Severe active CNS Lupus

Study Design

Total Participants: 51
Treatment Group(s): 5
Primary Treatment: Obinutuzumab
Phase: 1
Study Start date:
April 03, 2024
Estimated Completion Date:
August 31, 2027

Connect with a study center

  • Artiva Clinical Trial Site

    Birmingham, Alabama 35249
    United States

    Active - Recruiting

  • Artiva Investigational Site Birmingham

    Birmingham, Alabama 35249
    United States

    Active - Recruiting

  • University of Alabama at Birmingham (UAB)

    Birmingham, Alabama 35294
    United States

    Active - Recruiting

  • Artiva Clinical Trial Site

    Tucson, Arizona 85724
    United States

    Active - Recruiting

  • Artiva Investigational Site Tucson

    Tucson, Arizona 85724
    United States

    Active - Recruiting

  • Artiva Clinical Trial Site

    Foster City, California 75150
    United States

    Site Not Available

  • Artiva Clinical Trial Site

    San Diego, California 92121
    United States

    Active - Recruiting

  • Artiva Investigational Site San Diego

    San Diego, California 92121
    United States

    Active - Recruiting

  • University of California, San Diego

    San Diego, California 92121
    United States

    Active - Recruiting

  • Artiva Clinical Trial Site

    Aventura, Florida 33180
    United States

    Active - Recruiting

  • Artiva Investigational Site Aventura

    Aventura, Florida 33180
    United States

    Active - Recruiting

  • Artiva Clinical Trial Site

    Plantation, Florida 33324
    United States

    Active - Recruiting

  • Artiva Investigational Site Plantation

    Plantation, Florida 33324
    United States

    Active - Recruiting

  • Artiva Clinical Trial Site

    Iowa City, Iowa 52242
    United States

    Active - Recruiting

  • Artiva Investigational Site Iowa

    Iowa City, Iowa 52242
    United States

    Active - Recruiting

  • Artiva Clinical Trial Site

    Charlotte, North Carolina 28625
    United States

    Active - Recruiting

  • Artiva Investigational Site Charlotte

    Charlotte, North Carolina 28625
    United States

    Active - Recruiting

  • Artiva Clinical Trial Site

    Statesville, North Carolina 28625
    United States

    Site Not Available

  • Artiva Clinical Trial Site

    Mesquite, Texas 75150
    United States

    Active - Recruiting

  • Artiva Investigational Site Mesquite

    Mesquite, Texas 75150
    United States

    Active - Recruiting

  • Artiva Clinical Trial Site

    The Woodlands, Texas 77382
    United States

    Active - Recruiting

  • Artiva Investigational Site Woodlands

    The Woodlands, Texas 77382
    United States

    Active - Recruiting

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.