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RecruitingPhase 1

US Zamto-cel Autoimmune Diseases

Miltenyi Biomedicine GmbH · NCT06708845

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Phase 1
Target enrollment
48
US sites recruiting
1
Study start
July 2026
Record last updated
June 11, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

AID is a phase I multi-cohort study to assess the safety and tolerability of zamtocabtagene autoleucel (zamto-cel) in patients with refractory autoimmune diseases (SLE-Non renal, SLE-LN, SSc/dcSSc) after receiving standard therapy.

Being studied: zamtocabtagene autoleucel; Cyclophosphamide; Fludarabine

Conditions: Lupus Nephritis; Systemic Lupus Erythematosus; Systemic Sclerosis (SSc); Diffuse Cutaneous Systemic Sclerosis

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

General Key Inclusion/Exclusion Criteria Across All Cohorts

Inclusion Criteria

•Confirmed diagnosis of autoimmune disease (SLE-Non-renal, SLE-LN, SSc/ dcSSc)

Exclusion Criteria

  • Prior gene therapy treatment
  • Active malignancy within past 5 years
  • Significant active fungal or bacterial infection
  • History or presence of CNS lupus or other CNS disease
  • eGFR \< 45 mL/min/1.73 m\^2
  • Total bilirubin outside the normal range (unless congenital hyperbilirubinemia such as Gilbert syndrome has been confirmed).

Systemic Lupus Erythematosus-Non-renal Key Inclusion/Exclusion Criteria

Inclusion Criteria

  • Positive for at least 1 of the following autoantibodies at Screening: anti- double stranded DNA or anti-Smith
  • Systemic Lupus Erythematosus Disease Activity Index-2000 score ≥ 8 AND at least 1 British Isles Lupus Assessment Group (BILAG)-2004 Class A (severe manifestation) organ scores
  • Inadequate response to glucocorticoids and to at least 2 of the following treatments, used for at least 3 months each: cyclophosphamide, mycophenolic acid or its derivatives, belimumab, azathioprine, anifrolumab, methotrexate, rituximab, or obinutuzumab

Exclusion Criteria

  • Subjects with neuropsychiatric SLE.
  • Drug-induced SLE.

Systemic Lupus Erythematosus - Lupus Nephritis Key Inclusion/Exclusion Criteria

Inclusion Criteria

  • Positive for at least 1 of the following autoantibodies at Screening: anti- double stranded DNA or anti-Smith
  • Confirmed LN diagnosis by kidney biopsy during screening or within the previous 6 months, with severe active phase of the disease.
  • Progressing despite maintenance on maximally tolerated doses of renin- angiotensin system (RAS) blocking agents, unless allergic to or intolerant of ACE inhibitors and ARBs
  • Inadequate response to glucocorticoids and hydroxychloroquine and at least 1 of the following treatments, used for at least 3 months each: cyclophosphamide, mycophenolic acid derivatives, belimumab, azathioprine, methotrexate, rituximab, obinutuzumab, calcineurin inhibitor (cyclosporin, tacrolimus or voclosporin)

Exclusion Criteria

•Evidence of Rapidly progressive glomerulonephritis (defined as a doubling of serum creatinine within 3 months prior to enrollment) or as determined by the study investigator.

Systemic Sclerosis/Diffuse Cutaneous Systemic Sclerosis Cohort Key Inclusion/ Exclusion Criteria

Inclusion Criteria

  • Active disease defined as:
  • Modified Rodnan skin score (mRSS) ≥ 16 units, in the prior 6 months, with 1 or more of the following:
  • Increase in mRSS by ≥ 3 units or 10%
  • Involvement of 1 new body area with increase in mRSS by ≥ 2 units
  • Involvement of 2 new body areas with increase by ≥ 1 mRSS unit OR
  • Progressive interstitial lung disease (ILD) defined as:
  • Worsening of respiratory symptoms and an increased extent of fibrosis evaluated by high-resolution computed tomography
  • Lack of response to standard therapy (e.g., failure of ≥ 2 immunosuppressive therapies)

Exclusion Criteria

  • "Active" gastric antral vascular ectasia, as evidenced by bleeding (ie, on esophagogastroduodenoscopy) in the past 6 months or as per Investigator's assessment.
  • History of SSc renal crisis within 1 year prior to Screening; presence of kidney impairment due to conditions other than SSc

Recruiting US locations

  • Froedtert Hospital and the Medical College of Wisconsin

    Milwaukee, WI 53226

    Site contact: Kiley Timler · ktimler@mcw.edu

Study contacts (from the official record)

  • Sadie Swift · 617-218-0044 · clinicaltrials@miltenyi.com
  • Paris Jamiel · 617-218-0044 · clinicaltrials@miltenyi.com
All phase 1 studies in Wisconsin →
US Zamto-cel Autoimmune Diseases (NCT06708845) | Bored Studies