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

NCT07261631

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

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

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Pancreatic Ductal Adenocarcinoma
  • Non-Small Cell Lung Cancer
  • HR+/HER2- Ductal and Lobular Breast Cancer
  • Triple Negative Breast Cancer
  • Colorectal Cancer
  • Soft Tissue Sarcoma

Eligibility basics and study details

Study type
Interventional
Phase
Phase 1
Ages
18 years and older
Sex
All
Healthy volunteers
Not accepted
Sponsor
Novartis Pharmaceuticals
Last updated on ClinicalTrials.gov
October 9, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

New Jersey · 1

  • United Theranostics · Princeton, NJ

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.