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Recruiting Phase 1

Phase I Study of [177Lu]Lu-DFC413 in Patients With Solid Tumors

NCT07261631 · tracked via the Priya Life Science USA tracker
Phase
Phase 1
Started
2025-11-24
Last updated
2026-06-17

Condition(s) studied

Pancreatic Ductal AdenocarcinomaNon-Small Cell Lung CancerHR+/HER2- Ductal and Lobular Breast CancerTriple Negative Breast CancerColorectal CancerSoft Tissue Sarcoma

Investigational drug(s) / intervention(s)

68Ga-NNS309 →177Lu-DFC413

68Ga-NNS309: Diagnostic investigational radiopharmaceutical

177Lu-DFC413: Therapeutic investigational radiopharmaceutical

Study summary

The purpose of this study is to evaluate the safety, tolerability, dosimetry and preliminary efficacy of \[177Lu\]Lu-DFC413 and safety and imaging properties of \[68Ga\]Ga-NNS309 in patients aged ≥ 18 years with solid tumors

Eligibility

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: * Adults ≥ 18 years with one of the following indications: * Locally advanced unresectable or metastatic PDAC, with disease progression following, or intolerance to cytotoxic therapy, unless patient was ineligible to receive such therapy * Locally advanced unresectable or metastatic NSCLC without any actionable genomic alterations with disease progression following, or intolerance to chemotherapy and immunotherapy, unless patient was ineligible to receive such therapy, or locally advanced unresectable or metastatic NSCLC with an actionable genomic alteration with disease progression following, or intolerance to chemotherapy and targeted therapy, unless patient was ineligible to receive such therapy * Locally advanced unresectable or metastatic HR+/HER2- ductal and lobular breast cancer with disease progression following, or intolerance to, hormone therapy and CDK inhibitor, and at least one additional line of therapy, unless patient was ineligible to receive such therapy * Locally advanced unresectable or metastatic triple negative breast cancer (TNBC) with disease progression following, or intolerance to, at least two lines of therapy, unless patient was ineligible to receive such therapy * Locally advanced or metastatic unresectable CRC with disease progression following, or intolerance to cytotoxic chemotherapy, unless patient was ineligible to receive such therapy. Patients with known microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) status must also have had disease progression following, or intolerance to, immune checkpoint inhibitor therapy, unless patient was ineligible to receive such therapy * (Dose expansion only) Locally advanced unresectable or metastatic soft tissue sarcoma (excluding GIST and Kaposi) with disease progression following, or intolerance to, at least one line of systemic therapy * Patients must have lesions showing 68Ga-NNS309 uptake Exclusion Criteria: * Absolute neutrophil count (ANC) \< 1.5 x 109/L, hemoglobin \< 9 g/dL, or platelet count \< 100 x 109/L * QT interval corrected by Fridericia's formula (QTcF) ≥ 470 msec * eGFR \< 60 mL/min/1.73m2, calculated using CKD-EPI 2021 or measured * Unmanageable urinary tract obstruction or urinary incontinence * Presence of symptomatic CNS metastases, or CNS metastases that require local CNS-directed therapy * Any prior radioligand therapy * Radiation therapy within 4 weeks prior to the first dose of \[177Lu\]Lu-DFC413 Other protocol-defined inclusion/exclusion criteria may apply.

Primary outcome measure(s)

  • Incidence and severity of dose limiting toxicities of 177Lu-DFC413 — Within first treatment cycle, up to maximum 6 weeks
    A dose limiting toxicity (DLT) is defined as any adverse event or abnormal laboratory value of CTCAE (version 5.0) Grade 3 or higher that occurs within the DLT evaluation period and that is not primarily related to disease, disease progression, intercurrent illness, or concomitant medications with a few exceptions defined in the study protocol. Other clinically significant toxicities may be considered to be DLTs, even if not Grade 3 or higher.
  • Incidence and severity of adverse events and serious adverse events of 177Lu-DFC413 — From study treatment start up to approximately 42 months
    The distribution of adverse events will be done via the analysis of frequencies for treatment emergent Adverse Event (TEAEs) and Serious Adverse Event (TESAEs) and through the monitoring of relevant clinical and laboratory safety parameters.
  • Dose modifications for 177Lu-DFC413 — From study treatment start until last dose of study treatment, assessed up to approximately 24 weeks
    Dose modifications (dose interruptions and reductions) for 177Lu-DFC413 will be assessed and summarized using descriptive statistics. The number of patients with dose modification and the reasons will be summarized by treatment groups.
  • Dose intensity for 177Lu-DFC413 — From study treatment start until last dose of study treatment, assessed up to approximately 24 weeks
    Dose intensity for 177Lu-DFC413 will be assessed and summarized using descriptive statistics. Dose intensity is computed as the ratio of actual cumulative dose received and actual duration of exposure.

Trial sites (8)

FacilityCityRegionStatus
Novartis Investigative Site Montreal Quebec Recruiting
Novartis Investigative Site Odense C Denmark Recruiting
Novartis Investigative Site Vandœuvre-lès-Nancy France Recruiting
Novartis Investigative Site Essen Germany Recruiting
Novartis Investigative Site Haifa Israel Recruiting
Novartis Investigative Site Tel Aviv Israel Recruiting
Novartis Investigative Site Singapore Singapore Recruiting
Novartis Investigative Site Singapore Singapore Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07261631 on ClinicalTrials.gov ↗ ← All trials in the USA