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OncoMatch/Clinical Trials/NCT04789486

Nano-SMART: Nanoparticles With MR Guided SBRT in Centrally Located Lung Tumors and Pancreatic Cancer

Is NCT04789486 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies AGuIX for non-small cell lung cancer.

Phase 1/2RecruitingDana-Farber Cancer InstituteNCT04789486Data as of May 2026

Treatment: AGuIXThis research study is being done to help determine the safety and efficacy of gadolinium based nanoparticle, Activation and Guidance of Irradiation X (AGuIX), used in conjunction with MR-guided stereotactic body radiation therapy (SBRT) in the treatment of pancreatic cancer and lung tumors.

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Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Pancreatic Cancer

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Must have received: induction chemotherapy (FOLFIRINOX, gemcitabine and nab-paclitaxel) — locally advanced pancreatic cancer

Completion of at least 3 months of standard induction chemotherapy for LAPC, which should consist of either FOLFIRINOX, gemcitabine and nab-paclitaxel, or another standard combination of induction chemotherapy agent, with a washout period no longer than 10 weeks prior to first dose of study drug.

Cannot have received: radiation therapy

Participants who have had prior radiation therapy to the chest or abdomen that would overlap with the current treatment field.

Lab requirements

Blood counts

absolute neutrophil count ≥1,500/mcL; platelets ≥100,000/mcL

Kidney function

creatinine within normal institutional limits OR creatinine clearance ≥60 mL/min/1.73 m2 for participants with creatinine levels above institutional normal

Liver function

total bilirubin within normal institutional limits; AST(SGOT)/ALT(SGPT) ≤2.5 × institutional upper limit of normal

Participants must have normal organ and marrow function as defined below: absolute neutrophil count ≥1,500/mcL; platelets ≥100,000/mcL; total bilirubin within normal institutional limits; AST(SGOT)/ALT(SGPT) ≤2.5 × institutional upper limit of normal; creatinine within normal institutional limits OR creatinine clearance ≥60 mL/min/1.73 m2 for participants with creatinine levels above institutional normal.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Brigham and Women's Hospital · Boston, Massachusetts
  • Dana Farber Cancer Institute · Boston, Massachusetts

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