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

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

Trial Details

NCT ID
NCT07261631
Phase
PHASE1
Sponsor
Novartis Pharmaceuticals
Status
RECRUITING
Cancer Type
Lobular Carcinoma Breast Cancer
Interventions
  • 68Ga-NNS309
  • 177Lu-DFC413
Locations (sample)
  • Montreal, Quebec, Canada|45.50884,-73.58781
  • Odense C, Denmark|55.40841,10.39538
  • Vandœuvre-lès-Nancy, France|48.66115,6.17114
  • Haifa, Israel|32.81303,34.99928
  • Tel Aviv, Israel|32.08088,34.78057

Key Eligibility 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 ineli…
  • Locally advanced unresectable or metastatic NSCLC without any actionable genomic alterations with disease progression following, or intolerance to …
  • Locally advanced unresectable or metastatic HR+/HER2- ductal and lobular breast cancer with disease progression following, or intolerance to, hormo…

For full eligibility, visit ClinicalTrials.gov.

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