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Active, not recruiting Phase 2 Interventional

A Study of Rapcabtagene Autoleucel in Active, Refractory Systemic Lupus Erythematosus (SLE) or Lupus Nephritis (LN) Patients (AUTOGRAPH - SLE/LN)

ClinicalTrials.gov ID: NCT06581198

Public ClinicalTrials.gov record NCT06581198. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 7, 2026, 8:54 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Open-label, Study to Evaluate the Efficacy and Safety of Rapcabtagene Autoleucel in Patients With Active, Refractory Systemic Lupus Erythematosus (SLE) or Active, Refractory Lupus Nephritis (LN).

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the efficacy and safety of rapcabtagene autoleucel (administered once following lymphodepletion) in patients with active, refractory systemic lupus erythematosus (SLE) or active, refractory lupus nephritis (LN).

Study identification

NCT ID
NCT06581198
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
179 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 3, 2024
Primary completion
Feb 13, 2028
Completion
Feb 5, 2032
Last update posted
Sep 1, 2026

2024 – 2032

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
University Of Alabama Birmingham Alabama 35294
Loma Linda University San Bernardino California 92408
UCSF San Francisco California 94115
Sutter Health Network San Pablo California 94806
Ann and Robert H Lurie Childs Hosp Chicago Illinois 60611
Northwestern University Chicago Illinois 60611
University Of Iowa Iowa City Iowa 52242
University of Kentucky Lexington Kentucky 40536-0284
Tufts Medical Center Boston Massachusetts 02111
Boston Medical Center Boston Massachusetts 02118
WA Uni School Of Med St Louis Missouri 63110
Duke Clinical Research Institute Durham North Carolina 27710
James Cancer Hospital Columbus Ohio 43210
Oregon Health Sciences University Portland Oregon 97239
Houston Methodist Hospital Houston Texas 77030
Univ Of TX MD Anderson CC Houston Texas 77030
LDS Hospital Salt Lake City Utah 84143

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 90 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06581198, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 1, 2026 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06581198 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →