Recurrent or Refractory Systemic Lupus ErythematosusEarly Phase 1NCT07339540

the Safety and Efficacy of Targeted BCMA In Vivo LV Injection for Recurrent or Refractory Autoimmune Diseases

A Early Phase 1 study testing V001-BCMA in people with Recurrent or Refractory Systemic Lupus Erythematosus and Recurrent or Refractory IgG4 Related Diseases, run by Tongji Hospital at 1 site in China.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record

Search all trials

Trial summary

This study is designed as a single arm, open label, single center clinical trial to evaluate the safety, tolerability, efficacy, pharmacokinetic or pharmacodynamic characteristics of the investigational drug V001-BCMA in autoimmune disease. Read more about this study

Who is it for?: Ages 18 to 65 years
Conditions the study is for: Recurrent or Refractory Systemic Lupus Erythematosus, Recurrent or Refractory IgG4 Related Diseases, Recurrent or Refractory Systemic Sclerosis
What is being tested?: V001-BCMA
Type of treatment: Injection or infusion
Could I receive a placebo?: No, everyone receives an active treatment
How many people: 45 participants
Where: 1 siteChina
Study dates: 4 Nov 2025to 30 Oct 2028
Phase: Early Phase 1

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

Ages 18 to 65 years
All sexes
No healthy volunteers
Adult, Older adult

Who may be able to join

1. The age at the time of signing the informed consent form is ≥18 years old and ≤65 years old;
2. For cohort 1: recurrent or refractory systemic lupus erythematosus (all of the following four items must be met simultaneously)
Diagnosed with SLE according to the 2012 SLICC or 2019 EULAR/ACR revised criteria.
During screening, the patient exhibits positive anti-nuclear antibodies, and/or positive anti-ds-DNA antibodies, and/or positive anti-Smith antibodies.
Before screening, patients must have received treatment with glucocorticoids combined with immunosuppressants and/or biologics for at least 3 months, with a stable dose for more than 2 weeks, and the disease remains active or the patient is intolerant to the medication.
During the screening period, the SLEDAI-2K score is ≥8 points

Show all 28Show fewer

3. For cohort 2: recurrent or refractory IgG4-related disease (all three of the following criteria must be met simultaneously)
Meet the American College of Rheumatology (ACR)/EULAR 2019 classification criteria for IgG4-RD.
Patients with clinical manifestations of recurrent or refractory IgG4-RD and ineffective conventional treatment
Meet the clinical phenotype of "Mikulicz-system involvement"
4. For cohort 3: relapsed or refractory systemic sclerosis (all of the following 5 items must be met simultaneously)
Meet the 2013 American College of Rheumatology (ACR) and European League Against Rheumatism (EULAR) classification criteria for SSc.
Anti-Scl 70 antibody positive, or anti-centromere protein antibody positive, or anti-RNA polymerase III antibody positive
Patients with a modified Rodnan skin score (mRSS) of ≥10 at screening
Before screening, patients must have received treatment with glucocorticoids combined with immunosuppressants and/or biologics for at least 3 months, with a stable dose for more than 2 weeks, and the disease remains active or intolerable.
5. For cohort 4: relapsed or refractory idiopathic inflammatory myopathies (all of the following 5 criteria must be met)
Meet the 2017 EULAR/ACR classification criteria for inflammatory myopathies (including dermatomyositis DM, polymyositis PM, anti-synthetase syndrome ASS, and necrotizing myositis NM).
At least one myositis-specific antibody (MSA) or myositis-associated antibody (MAA) positive (+ or above)
During the screening period, the patient meets 2 of the following criteria: PGA(VAS)≥2cm (VAS-10cm scale); PtGA(VAS)≥2cm (VAS-10cm scale); HAQ>0.25; one or more muscle enzymes are elevated (CK, LDH, AST, ALT) ≥1.5×ULN; overall muscle extrinsic assessment (MDAAT) ≥2.0cm (VAS-10cm scale)
After at least 3 months of treatment with glucocorticoids and immunosuppressants and/or biologics, with stable doses for more than 2 weeks, the disease remains active or the patient is intolerant to the medication.
Active myositis is present in muscle biopsy or muscle MRI during the screening period or within the first 6 months before the screening period.
6. For cohort 5: relapsed or refractory AAV (all three of the following conditions must be met simultaneously)
According to the 2022 ACR/EULAR criteria, the patient is diagnosed with AAV (GPA or MPA subtype). According to the KDIGO guidelines, after 3 months of treatment with glucocorticoids combined with immunosuppressants such as cyclophosphamide or biologics such as rituximab, and the dose is stable for more than 2 weeks, the disease is still active or the patient is intolerant to the drug;
The patient is currently or has been in the course of AAV related antibodies positive;
Severe disease requiring treatment (BVAS score ≥3.0).
7. Possess sufficient organ function
8. Men with fertility and women of childbearing age must agree to use effective contraception from the time they sign the informed consent form until 1 year after the study drug is administered. Blood pregnancy tests for women of childbearing age must be negative at screening and before infusion;
9. The subject or his/her guardian agrees to participate in this clinical study and signs the informed consent form (ICF), indicating that he/she understands the purpose and procedures of this clinical study and is willing to participate in the study.

Who cannot join

1. For cohort 1: relapsed or refractory systemic lupus erythematosus
Subjects with uncontrolled lupus crisis within 8 weeks before screening were assessed by the investigator as unsuitable for participation in this study.
Before screening, patients with clinically significant central nervous system diseases or pathological changes not caused by lupus, including but not limited to cerebrovascular accident, aneurysm, epilepsy, convulsion/convulsion, aphasia, stroke, severe brain injury, dementia, Parkinson's disease, cerebellar disease, brain organic syndrome, or mental illness, should be excluded.
2. For cohort 3: relapsed or refractory systemic sclerosis. High-risk pulmonary arterial hypertension, according to the "Risk Stratification of Arterial Pulmonary Arterial Hypertension (PAH)" in the "Guidelines for the Diagnosis and Treatment of Pulmonary Arterial Hypertension in China (2021 Edition)".
3. History of major organ transplantation (such as heart, lung, kidney, liver) or hematopoietic stem cell/bone marrow transplantation.
4. Subjects with a history of ≥ Grade 2 bleeding within 30 days prior to screening, as assessed by the investigator, were deemed unsuitable for enrollment.

Show all 23Show fewer

5. Use of any live vaccines against infectious diseases within 8 weeks before infusion.
6. Received any treatment using vesicular stomatitis virus G (VSVG) pseudotype virus.
7. The subject has a history or evidence of suicidal thoughts within 6 months before signing the ICF, or any suicidal behavior within 12 months before signing the ICF, and the researcher believes that there is a significant risk of suicide.
8. Pregnant or lactating women;
9. The patient has a history of severe and/or uncontrolled liver, gastrointestinal, kidney, lung, cardiovascular, psychiatric, neurological, or musculoskeletal diseases, hypertension, or any other medical condition that, in the opinion of the investigator, may affect the integrity of the patient's participation in the study, or may endanger the safety of the subject or affect the validity of the study results.
10. Suffered from malignant tumor within 3 years before screening, except for the following conditions: received radical treatment for malignant tumor and had no known active disease within ≥3 years before enrollment; or had fully treated non-melanoma skin cancer and currently had no evidence of disease;
11. Received any B-cell depleting biologic therapy (e.g., rituximab, ocrelizumab, obinutuzumab, ofatumumab, inebilizumab, etc.) within 3 months prior to infusion, unless B-cell recovery is proven.
12. Received immunosuppressants and other small molecule drugs within 3 days before infusion.
13. Use of any other clinical research drugs within 4 weeks before infusion. However, if the study treatment is ineffective or the disease progresses during the study period, and at least 3 half-lives have elapsed before screening, enrollment is allowed.
14. The patient has received live vaccines or live therapeutic infectious pathogens within 2 weeks before infusion.
15. The presence of chronic and active hepatitis B (excluding HBV-DNA levels below 500IU/ml), hepatitis C (HCV), human immunodeficiency virus (HIV) infection, or syphilis infection;
16. Active infection exists, requiring intravenous antibiotic therapy or hospitalization;
17. Patients who have undergone major surgery other than diagnosis or biopsy within 4 weeks before infusion, or are expected to undergo major surgery during the study period; note: patients who plan to undergo surgical procedures under local anesthesia can participate in the study.
Kyphoplasty or vertebroplasty are not considered major surgery;
18. Obvious evidence of cardiovascular disease as follows: a. N-terminal pro-B-type natriuretic peptide (NT-proBNP) > 8500ng/L; b. New York Heart Association (NYHA) classification of heart failure as III or IV; c. Patients who have received inpatient treatment for unstable angina or myocardial infarction within 6 months before the first dose, or who have received percutaneous coronary intervention and have received the latest stent placement within 6 months, or who have received coronary artery bypass grafting within 6 months;
19. Individuals who have known allergies, hypersensitivity reactions, intolerances, or contraindications to any component of V001-BCMA, or who have previously experienced severe allergic reactions.
20. Those who were deemed unsuitable for infusion or otherwise unsuitable for participation in the study by the researchers.

Trial locations and contacts

1 site in 1 country.

China1 site

Tongji Hospital, Affiliated to Tongji Medical College of Huazhong University of Science and Technology
Wuhan, Hubei, 430000

Other trials in China

About this study

Official title: Clinical Study on the Safety and Efficacy of Targeted BCMA In Vivo LV Injection in the Treatment of Recurrent or Refractory Autoimmune Diseases

Conditions: Recurrent or Refractory Systemic Lupus Erythematosus, Recurrent or Refractory IgG4 Related Diseases, Recurrent or Refractory Systemic Sclerosis, Recurrent or Refractory Idiopathic Inflammatory Myopathy, Recurrent or Refractory ANCA Associated Vasculitis
Being tested: V001-BCMA
Medical subject headings: Recurrence, Lupus Erythematosus, Systemic, Immunoglobulin G4-Related Disease, Scleroderma, Systemic, Myositis, Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

V001-BCMADrug
Targeted BCMA In-vivo LV Injection (Code: V001-BCMA) is a third-generation non-replicating self-inactivating lentiviral vector. Its envelope protein has been engineered to express targeting molecules on the lentiviral surface for specific recognition of T cells, while its nucleic acid contains a T cell-specific promoter and a CAR gene. After specifically targeting and binding to T cells, V001-BCMA enables the expression of CAR on the surface of T cells, forming CAR-T cells. These CAR-T cells can then specifically kill target cells.

Study groups in NCT07339540
Study group	Role	What they receive
V001-BCMA injection	Experimental	Not described Receives: Drug: V001-BCMA

What is being measured

The primary outcome is the main question the study is designed to answer.

The incidence of adverse events of V001-BCMA single infusion.
For all participants
Measured: At Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion

Secondary outcomes (53)

BILAG-2004 Scale Score
The BILAG-2004 index assesses disease activity in systemic lupus erythematosus (SLE) to guide treatment. It evaluates nine organ systems separately, grading each from A to E based on clinical features: A (severe, requiring aggressive therapy), B (moderate), C (mild), D (previous involvement), and E (no involvement). Its focus is on tracking changes per system for targeted management.
Measured: At baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
PGA
Physician Global Assessment. PGA score is used to assess the disease activity status of patient by physician. PGA min-max(0-3, the higher score represents the worse result)
Measured: At baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
SF-36
The 36-Item Short Form Health Survey. For SLE and AAV. SF-36 score min-max(0-100,the higher score represents the better result)
Measured: At baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
DORIS score
The DORIS score defines remission criteria in systemic lupus erythematosus (SLE), guiding treatment goals and trial endpoints. Its core assessment includes: 1) clinical SLEDAI=0; 2) Physician Global Assessment (PGA)<0.5; 3) prednisone ≤5mg/day; 4) stable immunosuppressive/biologic therapy. It also requires stable/improved serology and sustained duration of remission.
Measured: At Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
LLDAS
The LLDAS defines a "low disease activity state" in SLE, a key treatment target linked to better long-term outcomes. Core criteria include: 1) SLEDAI-2K ≤4; 2) no new disease activity; 3) Physician Global Assessment (PGA) ≤1.0; 4) prednisone ≤7.5mg/day; 5) stable immunosuppressive/biologic doses.
Measured: At Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Renal function response
Only for LN patients
Measured: At Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Cmax
For all subjects. Parameters of CAR copy number
Measured: Baseline, Day 2, Day 6, Day 10, Day 14, Day 21, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, Month 24
Tmax
For all subjects
Measured: Baseline, Day 2, Day 6, Day 10, Day 14, Day 21, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, Month 24
AUC0-28d
For all subjects
Measured: Baseline, Day 2, Day 6, Day 10, Day 14, Day 21, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, Month 24
AUC0-90d
For all subjects
Measured: Baseline, Day 2, Day 6, Day 10, Day 14, Day 21, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, Month 24
Tlast
For all subjects
Measured: Baseline, Day 2, Day 6, Day 10, Day 14, Day 21, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, Month 24
24-hour urine protein
Only for LN
Measured: Baseline, Day 2, Day 6, Day 10, Day 14, Day 21, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, Month 24
UPCR
UPCR (Urine Protein-to-Creatinine Ratio) is a key index to measure assessing treatment response in lupus nephritis.
Measured: Baseline, Day 2, Day 6, Day 10, Day 14, Day 21, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, Month 24
Proportion of CAR-T cells in T cells
For all subjects
Measured: baseline、Day 2、Day 6、Day 10、Day 14、Day 21、Day 28 after infusion
serum sBCMA level
BCMA expression levels of memory B cells and plasma blast cells in peripheral blood
Measured: Screening period, baseline, Day 14, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 post-infusion.
Time to disease recurrence
For IgG4-RD. Defined as the number of days between the day of infusion and the date of first treatment for IgG4-RD recurrence, as determined by a clinical professional, during the follow-up period
Measured: through study completion (at most 52 weeks)
Changes in lymphocyte subpopulations
For all subjects
Measured: Screening period, Day 14, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion, and at recurrence
Proportion of patients with improved disease activity (IgG4-RD RI)
For IgG4-RD. Improvement is defined as a decrease of ≥2 from the baseline disease activity score
Measured: Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
annualized recurrence rate
For IgG4-RD
Measured: through study completion, an average of 1 year
The proportion of subjects who achieved complete remission without relapse at week 52
For IgG4-RD
Measured: at week 52
Change in CRISS-25 score from baseline
For systemic sclerosis. The score of CRISS-25 min-max(0-1.0, the higher score represents the better result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Change in forced vital capacity (FVC) (mL) from baseline
For systemic sclerosis
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Change in mRSS from baseline
For systemic sclerosis. The score of mRSS min-max(0-51, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Change from baseline in Quantitative Interstitial Lung Disease (QILD) imaging score
For systemic sclerosis. The min-max score (0-100%, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Change from baseline in Quantitative Lung Fibrosis (QLF) imaging score
For systemic sclerosis. The min-max score (0-100%, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in Scleroderma Patient Skin Report (SSPRO) compared to baseline
For systemic sclerosis.The min-max score (0-108, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in Scleroderma Clinical Trial Consortium Damage Index (SCTC-DI) compared to baseline
For systemic sclerosis. The min-max score (0-55, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in EUSTAR activity index scores compared to baseline
For systemic sclerosis The min-max score (0-10, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in Capillaroscopic skin ulcer risk index (CSURI) compared to baseline
For systemic sclerosis. CSURI is a continuous variable; the higher the score, the greater the ulcer risk.
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in Gastrointestinal questionnaire scores of the University of California, Los Angeles Scleroderma Clinical Trial Alliance compared to baseline
For systemic sclerosis.The min-max score (0-3, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in serum SSc-related antibodies compared to baseline
For systemic sclerosis
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in Muscle Strength Score (MRC) compared to baseline
For idiopathic inflammatory myopathies. The min-max score (0-60, the higher score represents the better result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
The changes in total improvement score (TIS) compared to baseline
For idiopathic inflammatory myopathies. The min-max score (0-100, the higher score represents the better result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in lesion size and severity index (CDASI) compared to baseline
For idiopathic inflammatory myopathies. The CDASI is a core instrument for assessing the severity of cutaneous dermatomyositis. It consists of two independent subscales: Activity (scored 0-100, with higher scores indicating worse status) and Damage (scored 0-32, with higher scores indicating worse status).
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Physician's overall disease activity score
For idiopathic inflammatory myopathies. The min-max score (0-10, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in Manual Muscle Testing 8 (MMT8) compared to baseline
For idiopathic inflammatory myopathies. The min-max score (0-150, the higher score represents the better result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in Expanded Myositis Disease Activity Index (EMDA) compared to baseline
For idiopathic inflammatory myopathies. The min-max score (0-10, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in MDAAT score compared to baseline
For idiopathic inflammatory myopathies. the overall score of extramuscular disease activity was assessed using the MDAAT scoring tool. The min-max score (0-60, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Myositis Core Set Measures
For idiopathic inflammatory myopathies
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
the remission rate of myositis (defined as an increase in TIS of ≥20, ≥40, and ≥60 points) was assessed according to the 2016 ACR/EULAR criteria for myositis remission
For idiopathic inflammatory myopathies
Measured: Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Time to improvement (TIS≥20, ≥40 and ≥60)
For idiopathic inflammatory myopathies
Measured: up to 52 weeks
Duration of remission (time from clinical remission to deterioration/time from remission to first recurrence)
For idiopathic inflammatory myopathies
Measured: up to 52 weeks
Changes in myositis specific antibodies and myositis associated antibodies in serum compared to baseline after injection
For idiopathic inflammatory myopathies
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in ILD on CT imaging compared to baseline (only for patients with ILD at baseline)
For idiopathic inflammatory myopathy patients with ILD in the baseline period
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Pulmonary function examination evaluates changes in ventilation and diffusion function compared to baseline
For idiopathic inflammatory myopathies. Pulmonary function examination can comprehensively evaluate the ventilation function, air exchange function, and airway responsiveness of the lungs, which is of great significance for the diagnosis, condition evaluation, and efficacy judgment of respiratory diseases
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Myositis specific antibody levels
For idiopathic inflammatory myopathies
Measured: Screening period, baseline, Day 14, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 post-infusion.
Myositis related antibody levels
For idiopathic inflammatory myopathies
Measured: Screening period, baseline, Day 14, Day 28, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 post-infusion.
The proportion of subjects who maintained remission
For AAV
Measured: Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
duration of response
For AAV
Measured: Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in Vasculitis Damage Index (VDI) scores compared to baseline
For AAV
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in quality of life (SF-36 V2 scale) scores compared to baseline
For AAV. The min-max score (0-100, the higher score represents the better result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in Disease Scope Index (DEI) compared to baseline
For AAV. The min-max score (0-21, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion
Changes in Five Factor Score (FFS) compared to baseline
For AAV. The min-max score (0-5, the higher score represents the worse result)
Measured: At Baseline, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 18, and Month 24 after infusion

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

4 Nov 202530 Oct 2028

First posted14 Jan 2026
Study start4 Nov 2025
Primary completion30 Oct 2028 (estimated)
Study completion30 Oct 2028 (estimated)

Resources

Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
Other trials for Recurrent or Refractory Systemic Lupus ErythematosusStudies of the same condition, open and under way.
What the trial phases meanHow a treatment moves from first tests in people to approval.

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design

Study type: Interventional
Phase: Early Phase 1
Primary purpose: Treatment
Allocation: Not applicable
Intervention model: Single group
Masking: None (open label)
Enrolment: 45 participants (estimated)

IDs, dates and publications

ClinicalTrials.gov ID: NCT07339540
Sponsor's protocol ID: PRG2503E2
Status last verified: Sep 2026
First submitted: 26 Nov 2025
Last updated: 17 Sep 2026
Results posted: No
Data monitoring committee: No
FDA-regulated drug: No
FDA-regulated device: No