CAR-DC for End-Stage IPF (NCT07329959) | Clinical Trial Compass
Not Yet RecruitingPhase 1
CAR-DC for End-Stage IPF
8 participantsStarted 2026-02-01
Plain-language summary
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, fatal interstitial lung disease characterized by irreversible scarring, leading to respiratory failure. With limited treatment options and a poor prognosis, new therapies are urgently needed. This study investigates a novel cell therapy targeting pathological fibroblasts, a key driver of fibrosis.
Single-cell analyses identify CTHRC1+FAP+ fibroblasts as a collagen-producing subpopulation crucial in IPF progression. Chimeric antigen receptor (CAR) technology enables precise targeting of these cells. While CAR-Treg therapy has shown promise in preclinical models, its clinical translation requires careful safety evaluation regarding infection risk, potential tumor promotion, and immune reconstitution.
This trial employs an innovative approach using engineered dendritic cells (DCs). CAR technology is applied to generate immunosuppressive CAR-DCs (iCAR-DCs) designed to target FAP, localize to fibrotic lung areas, and attenuate fibrosis without eliciting a detrimental immune response. Preliminary mouse studies demonstrated that iCAR-DC administration following lung injury significantly reduced fibrosis without apparent organ toxicity and improved survival.
This single-arm trial aims to evaluate the efficacy and safety of this immunosuppressive CAR-DC therapy in patients with end-stage IPF. Key assessments will include changes in lung function, fibrosis extent on imaging, and comprehensive monitoring of potential adverse effects, particularly infections, tumor markers, and immune parameters.
Who can participate
Age range18 Years – 75 Years
SexALL
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Inclusion criteria
✓. A decline in forced vital capacity (FVC) ≥10% over a 6-month follow-up period.
✓. A decline in diffusing capacity of the lungs for carbon monoxide (DLCO) ≥10% of predicted value over 6 months.
✓. Six-minute walk test results showing oxygen saturation \<88%, a distance walked \<250 meters, or a decline of \>50 meters in distance over 6 months.
✓. Presence of pulmonary hypertension (PH) confirmed by right heart catheterization or transthoracic echocardiography.
✓. Hospitalization due to respiratory functional decline, pneumothorax, or acute exacerbation.
Exclusion criteria
✕. History of acute exacerbation of IPF within 4 weeks prior to screening or during the screening period.
✕. Presence of interstitial lung disease (ILD) other than IPF, including but not limited to: other forms of idiopathic interstitial pneumonia; ILD associated with fibrogenic agents, environmental exposures, or drug toxicity; other occupational lung diseases; granulomatous lung diseases; pulmonary vascular diseases; or ILD related to systemic diseases (e.g., vasculitis, infections such as tuberculosis, connective tissue diseases). Cases with uncertain diagnosis require serological testing and/or multidisciplinary team review for confirmation.
What they're measuring
1
The safety and efficacy of targeted FAP immunosuppressive CAR-DC in the treatment of end-stage idiopathic pulmonary fibrosis
Timeframe: Within six months after CAR-DC therapy
Trial details
NCT IDNCT07329959
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University
✕. History of malignancy, except for malignancies treated with curative intent and with no recurrence for ≥5 years, resected basal cell or squamous cell skin carcinoma, carcinoma in situ of the cervix, or resected colonic polyps.
✕. Significant history of infectious diseases.
✕. Presence of psychiatric illness or other conditions that would compromise the patient's ability to cooperate with study requirements, comply with treatment, or undergo monitoring.
✕. Known hypersensitivity to any component of the immunosuppressive CAR-DC cell product.
✕. History of severe renal failure requiring renal dialysis, or serum creatinine level \>2.5 mg/dL.