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NCT06265220 · ClinicalTrials.gov registry record · Phase 1
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
A Phase 1 study of SLE and Lupus Nephritis - WHO Class IV, sponsored by Artiva Biotherapeutics.
- Active
- Registry status
- Phase 1
- Development phase
- 51
- Enrollment target
- 9
- Study locations
NCT06265220 is a Phase 1 study of SLE and Lupus Nephritis - WHO Class IV that is active but no longer recruiting, run by Artiva Biotherapeutics. The registered enrollment target is 51 participants, below the 84-participant average among 9 other SLE trials with a reported enrollment target (39% lower). The trial reports 9 study locations across 7 states.
The verdict
NCT06265220, a Phase 1 study of SLE and Lupus Nephritis - WHO Class IV, is active but no longer recruiting, sponsored by Artiva Biotherapeutics.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 1
- Development phase
- 51 participants
- Enrollment target
- 9
- Study locations
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.
Conditions Studied
Interventions
- DRUG AB-101
- DRUG Cyclophosphamide
- DRUG Fludarabine
- DRUG Rituximab
- DRUG Obinutuzumab
Study Locations (9)
Florida
- Artiva Investigational Site Aventura - Aventura
- Artiva Investigational Site Plantation - Plantation
Texas
- Artiva Investigational Site Mesquite - Mesquite
- Artiva Investigational Site Woodlands - The Woodlands
Alabama
- Artiva Investigational Site Birmingham - Birmingham
Arizona
- Artiva Investigational Site Tucson - Tucson
California
- Artiva Investigational Site San Diego - San Diego
Iowa
- Artiva Investigational Site Iowa - Iowa City
North Carolina
- Artiva Investigational Site Charlotte - Charlotte
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 51 participants |
| Start Date | 2024-04-03 |
| Est. Completion | 2027-08 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06265220
The ClinicalTrials.gov registry entry for NCT06265220 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 84-participant average among 9 other SLE trials with a reported enrollment target (39% lower). The listed sponsor is Artiva Biotherapeutics, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with SLE appearing as the primary indexed condition, and to 5 interventions - of which AB-101 is the first listed.
NCT06265220 reports 9 study locations spanning 7 distinct geographic areas - top geographies include Florida, Texas, Alabama.
Frequently Asked Questions
What is clinical trial NCT06265220 about?
NCT06265220 is a clinical study titled "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". 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 cli...
What is the current status of trial NCT06265220?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 51 participants. The study started on 2024-04-03. Estimated completion is 2027-08.
What conditions does trial NCT06265220 study?
This clinical trial studies the following conditions: SLE, Lupus Nephritis - WHO Class IV, Lupus Nephritis - WHO Class III, Refractory Systemic Lupus Erythematosus.
What interventions are being tested in trial NCT06265220?
The interventions under investigation include: AB-101 (DRUG), Cyclophosphamide (DRUG), Fludarabine (DRUG), Rituximab (DRUG), Obinutuzumab (DRUG).
Who is sponsoring clinical trial NCT06265220?
This trial is sponsored by Artiva Biotherapeutics, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06265220 being conducted?
This trial has 9 study locations across Alabama, Arizona, California, Florida, Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.