← Back to Search

CAR T-cell Therapy

NKX019 for Lupus

Phase 1

Recruiting

Led By Anca D Askanase, MD, MPH

Research Sponsored by Columbia University

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Positive antinuclear antibodies (ANA) ≥ 1:80 at screening OR positive anti-dsDNA OR positive anti-Smith (anti-Sm) as determined by the local laboratory

Age: 18-65 years old at the time of informed consent

Must not have

Major surgery within 28 days prior to the first dose of NKX019 or any surgery from which the subject has not recovered or has ongoing complications

Pregnancy, breast feeding or, if of childbearing potential, not using adequate contraceptive precautions or planned oocyte and sperm donation

Timeline

Screening 3 weeks

Treatment Varies

Follow Up up to 2 years after nkx019 infusion

Awards & highlights

No Placebo-Only Group

Summary

This trial aims to test the safety and tolerability of a drug called NKX019 after lymphodepletion. Secondary objectives include evaluating the effectiveness of NKX019 in patients with lupus, studying how

Who is the study for?

This trial is for individuals with Systemic Lupus Erythematosus (SLE), a chronic autoimmune disease. Participants should have active symptoms and may or may not have lupus nephritis, which affects the kidneys. The full eligibility criteria are not provided, but typically include specific health requirements and no recent treatments that could interfere with the study.

What is being tested?

The trial is testing NKX019, a type of cell therapy targeting CD19 to treat SLE. It's given after 'lymphodepletion' using low doses of Cyclophosphamide to prepare the body. The study will check how safe it is, its effects on lupus symptoms, how long it stays in the body (PK), and if it causes any immune response against itself.

What are the potential side effects?

While specific side effects aren't listed here, similar therapies can cause infusion reactions, increased risk of infections due to immune system suppression by Cyclophosphamide LD, fatigue, nausea or other organ-specific inflammation as common issues.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Select...

I have tested positive for specific autoimmune markers.

Select...

I am between 18 and 65 years old.

Select...

My lupus hasn't improved after trying at least two different treatments for over 3 months.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:

Select...

I haven't had major surgery in the last 28 days or have fully recovered from any surgery without complications.

Select...

I am not pregnant, breastfeeding, and if capable of becoming pregnant, I am using effective birth control or not planning to donate eggs or sperm.

Select...

I have previously received cellular therapy, such as CAR-T.

Select...

I haven't taken any SLE treatments or experimental drugs within the last 4 weeks or 5 half-lives of the drug.

Select...

My kidney function, measured by eGFR, is below 45 mL/min/1.73 m2.

Select...

I am on dialysis or expected to need it during the study.

Select...

I have had or am planning to have an organ or bone marrow transplant.

Select...

I have a weak immune system that leads to severe infections or I am on long-term immune system boosting treatments.

Select...

I do not have severe liver disease or very high liver enzyme levels.

Select...

I have lung problems like COPD or asthma that need daily oral steroids, or my oxygen levels are low without extra oxygen.

Select...

I have smoked more than 10 pack-years.

Select...

I have needed steroids for COPD/asthma in the last 6 months.

Select...

My blood counts are low not because of my lupus.

Select...

I have tested positive for HIV, Hepatitis B or C, or have active or latent TB needing treatment.

Select...

I am not taking any medications that are not allowed in the study.

Select...

I am not allergic to the study drug or its components.

Select...

I do not have major heart issues, recent severe heart events, or active bleeding disorders.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ up to 2 years after nkx019 infusion

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~up to 2 years after nkx019 infusion

This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 2 years after nkx019 infusion for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.

Primary study objectives

Incidence of adverse events (AEs)

Secondary study objectives

Change from baseline in hybrid SLEDAI (Systemic Lupus Erythematosus Disease Activity Index) score

Change from baseline of autoantibody levels

Maximum concentration (Cmax) of PK in peripheral blood

+2 more

Awards & Highlights

No Placebo-Only Group

All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups

Experimental Treatment

Group I: NKX019 infusionExperimental Treatment2 Interventions

Subjects with SLE will receive cyclophosphamide LD followed by NKX019.

0 / 20Eligibility criteria met

Find a Location

Who is running the clinical trial?

Columbia UniversityLead Sponsor

1,486 Previous Clinical Trials

2,655,310 Total Patients Enrolled

Anca D Askanase, MD, MPHPrincipal InvestigatorColumbia University

1 Previous Clinical Trials

8 Total Patients Enrolled

~4 spots leftby Dec 2026

Unbiased ResultsWe believe in providing patients with all the options.

Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.

Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.

1045 Sansome St, Suite 321, San Francisco, CA

hello@withpower.com (415) 900-4227

About Us Treatment Support Dossier Update A Trial Listing

Conditions

Locations

Psychology Related

Treatments

Depression Trials Near You